The Association of Nighttime Fasting Duration and Prostate Cancer Risk: Results from the Multicase-Control (MCC) Study in Spain
by
, , , , ,
Anna Palomar-Cros
1,2,*
,
Ana Espinosa
1,2,3,4,
Kurt Straif
1,
Beatriz Pérez-Gómez
4,5,
Kyriaki Papantoniou
6, 
Inés Gómez-Acebo
4,7,
Ana Molina-Barceló
8,
Rocío Olmedo-Requena
4,9,10,
Juan Alguacil
4,11,
Guillermo Fernández-Tardón
4,12,13,
Delphine Casabonne
4,13,
Nuria Aragonés
4,5,
Gemma Castaño-Vinyals
1,2,3,4,
Marina Pollán
4,5,
Dora Romaguera
1,14,15 and
Manolis Kogevinas
1,2,3,4 1
Barcelona Institute for Global Health (ISGlobal), 08003 Barcelona, Spain
2
Department of Experimental and Health Sciences, Universitat Pompeu Fabra (UPF), 08003 Barcelona, Spain
3
Hospital del Mar Medical Research Institute (IMIM), 08003 Barcelona, Spain
4
Consortium for Biomedical Research in Epidemiology and Public Health (CIBERESP), Institute of Health Carlos III, 28029 Madrid, Spain
5
National Centre for Epidemiology, Carlos III Institute of Health, 28029 Madrid, Spain
6
Department of Epidemiology, Centre of Public Health, Medical University of Vienna, 1090 Vienna, Austria
7
Facultad de Medicina, Universidad de Cantabria—IDIVAL, 39011 Santander, Spain
8
Cáncer y Salud Pública, FISABIO, 46020 Valencia, Spain
9
Department of Preventive Medicine and Public Health, Universidad de Granada, 18016 Granada, Spain
10
Instituto de Investigación Biosanitaria de Granada (ibs.GRANADA), Hospitales Universitarios de Granada/Universidad de Granada, 18014 Granada, Spain
11
Centro de Investigación en Recursos Naturales, Salud y Medio Ambiente (RENSMA), Universidad de Huelva, Campus Universitario de El Carmen, 21071 Huelva, Spain
12
Instituto de Investigación Sanitaria del Principado de Asturias (ISPA) and IUOPA, Universidad de Oviedo, 33006 Oviedo, Spain
13
Cancer Epidemiology Research Programme IDIBELL, Institut Català d’Oncologia, 08908 L’Hospitalet de Llobregat, Spain
14
Health Research Institute of the Balearic Islands (IdISBa), 07120 Palma de Mallorca, Spain
15
CIBER Fisiopatología de la Obesidad y Nutrición (CIBEROBN), 28029 Madrid, Spain
*
Author to whom correspondence should be addressed.
Nutrients 2021, 13(8), 2662; https://doi.org/10.3390/nu13082662
Submission received: 21 June 2021
/
Revised: 22 July 2021
/
Accepted: 27 July 2021
/
Published: 30 July 2021
(This article belongs to the Section Nutrition and Public Health)
Abstract
:Nighttime fasting has been inconclusively associated with a reduced risk of cancer. The purpose of this study was to investigate this association in relation to prostate cancer risk. We examined data from 607 prostate cancer cases and 848 population controls who had never worked in night shift work from the Spanish multicase-control (MCC) study, 2008–2013. Through an interview, we collected circadian information on meal timing at mid-age. We estimated odds ratios (OR) and 95% confidence intervals (CI) with unconditional logistic regression. After controlling for time of breakfast, fasting for more than 11 h overnight (the median duration among controls) was associated with a reduced risk of prostate cancer compared to those fasting for 11 h or less (OR = 0.77, 95% 0.54–1.07). Combining a long nighttime fasting and an early breakfast was associated with a lower risk of prostate cancer compared to a short nighttime fasting and a late breakfast (OR = 0.54, 95% CI 0.27–1.04). This study suggests that a prolonged nighttime fasting duration and an early breakfast may be associated with a lower risk of prostate cancer. Findings should be interpreted cautiously and add to growing evidence on the importance of chrononutrition in relation to cancer risk.
1. Introduction
Prostate cancer is the most frequently diagnosed cancer in men and ranks as the third cause of cancer mortality in Spain [1]. Several non-modifiable risk factors for prostate cancer have been identified, including age, ethnicity and a family history of prostate cancer [2]. In 2019, following a first evaluation in 2007 of shift work that involves circadian disruption, the International Agency for Research on Cancer (IARC) classified night shift work as probably carcinogenic to humans, supported by limited evidence in humans for prostate, breast and colon cancer [3,4]. Circadian rhythms allow the adaptation to daily environmental changes and regulate multiple physiological activities in the organism following cycles of 24 h [5]. In the IARC report, several mechanistic hypotheses were proposed to explain the evaluated association, including chronic inflammation, hormonal alterations, cell proliferation and immunosuppression [3]. In the general population, circadian disruption as a result of exposure to artificial light-at-night (ALAN) [6,7], sleep duration [8,9,10] and mutations in clock genes [11], has also been associated with prostate cancer.
Although the light captured by the retina is the main synchronizer of the central circadian system, the feeding–fasting cycle also plays a major role in the regulation of peripheral clocks. Late-night eating has been associated with an increased prostate cancer risk in a study in France [12]. Similarly, previous results from the multicase-control (MCC) study in Spain found that having a long-time interval between supper and sleep was associated with a statistically significant reduced risk of prostate cancer [13]. This protective association was more pronounced in individuals with a morning chronotype, a human attribute believed to have a genetic basis that reflects a personal preference for timing of activity [13]. The morning chronotype was defined as having a mid-sleep time before 3:35 AM, based on the distribution among controls [13]. Results from the same study showed that having an early supper was associated with a reduced risk of prostate cancer, but results were not statistically significant [13]. Another study in adults reported an association between nighttime snacking and increased body fatness [14], the latter classified as a probable risk factor for prostate cancer [15,16].
Various fasting regimens have been associated with weight loss and have been recently popularized [17]. Intermittent fasting is a form of fasting that consists of restricting the feeding window to 8 h, therefore prolonging the nighttime fasting duration [17]. Prolonged nighttime fasting has also been associated with a reduction in waist circumference, blood glucose (HbA1c) levels and systemic inflammation, which may influence cancer risk [18,19]. Results from the prospective Women’s Healthy Eating and Living study suggested that fasting for 13 h or more reduced the risk of breast cancer recurrence compared to a shorter fasting period [20]. However, data from the NutriNet-Santé prospective cohort study showed that duration of fasting overnight was not significantly associated with the risk of developing prostate cancer [12]. Although nighttime fasting has been associated with a lower risk of cancer outcomes, skipping breakfast has been linked with an increased risk of low-grade inflammation [21].
Food behaviors, including time of supper and interval between supper and sleep, were previously examined in the MCC study [13]. However, the associations with nighttime fasting duration and time of breakfast were not evaluated. Given the current surge in fasting as a new food behavior, in this study we investigate whether prolonged nighttime fasting is associated with a reduced prostate cancer risk Additionally, we consider whether the time window of this period of fasting and the time of breakfast play an important role in this association.
2. Methods
2.1. Study Population
The MCC study (http://www.mccspain.org, accessed on 6 April 2021) is a multicase-control study conducted in 12 provinces of Spain between 2008 and 2013 [22]. Included in this analysis were individuals between the ages of 20 and 85 with histological confirmation of prostate cancer. As soon as possible after diagnosis, cancer cases were frequency matched based on age, sex and area with population controls. In each of the recruitment areas, administrative records from primary healthcare centers were reviewed to randomly select controls residing there for a minimum period of 6 months. For this study, participants who did not respond to the follow-up circadian interview (N = 522) were excluded (Figure 1). To avoid confounding, subjects ever doing night shift work were excluded (N = 535), with night shift work defined as working partly or entirely between midnight and 6 AM for 3 nights or more per month [13]. Participants with missing data on nighttime fasting (N = 93) were also excluded. In this analysis, 607 prostate cancer cases and 848 population controls from 7 different regions (Madrid, Barcelona, Asturias, Huelva, Cantabria, Valencia and Granada) were selected. Each of the Ethics committees of the included centers reviewed and approved the study protocol. All subjects signed a written informed consent.
2.2. Data Collection
A questionnaire was answered by participants in a face-to-face interview with a trained interviewer [22]. We requested information on age, sociodemographic factors, family history of prostate cancer, smoking, sleep duration, sleep problems and height and weight one year before the interview, from which the body mass index (BMI) was calculated as kg/m2. Exposure to indoor ALAN was assessed in the questionnaire through a Likert scale ranging from total darkness, almost dark and dim light to quite illuminated [6]. Outdoor ALAN exposure was also assessed but only for the cities of Barcelona and Madrid, where satellite images were available [6]. Light exposure was modeled and attributed to participants’ geocoded residences through Geographic Information System [6].
Following the interview, information on daily energy intake was gathered through a semi-quantitative food frequency questionnaire answered at home and estimated using the Centro de Enseñanza Superior de Nutrición y Dietética (CESNID) food composition table [23]. Ten percent of the participants did not respond to the food frequency questionnaire. A World Cancer Research Fund/American Institute of Cancer Research (WCRF/AICR) score was constructed [24]. The WCRF/AICR score ranged from 0 to 6 and included information on body fatness, physical activity, foods and drinks that promote weight gain, plant foods, animal foods and alcoholic drinks. This variable was further categorized into sex-specific tertiles based on the distribution in the control group [24].
Circadian data, including information on meal frequencies, duration and timings, were assessed through a telephone interview conducted 6 months to 5 years after the initial interview (median time 3 years) [13]. In this paper, we refer to these variables as dietary circadian variables. Participants reported their dietary circadian variables on weekdays and weekends at 40 years of age and during the year prior to the initial interview. Participants younger than 40 years of age were only asked for the information on the year prior to recruitment. Participants were also asked questions on sleep and timing of physical activity and answered the Munich Chronotype Questionnaire [13]. Chronotype was estimated as the standard mid-sleep time on free days, Mid-sleep time on free days (MSF) = [sleep onset on a free day + (sleep duration on free day/2)], and mid-sleep time on free days corrected for oversleeping on free days (MSFcorr) = MSF − [sleep duration on a free day − (sleep duration on a working day/2)]. Further details have been described elsewhere [13].
2.3. Exposure and Outcome Assessment
Nighttime fasting duration was defined as the period elapsed between the last eating episode before going to sleep and the first episode the following day. In the previous paper from MCC, we investigated time of supper [13], but now time of last intake also considered after supper snacks. For participants reporting not having breakfast, lunch was considered as breakfast, understood as the wider concept of breaking the nightly fast. The cut-off point for nighttime fasting distribution was set at 11 h (the median distribution among controls), defining a categorical variable with two levels: 11 h or less of fast, the reference category, versus more than 11 h of fast. We based the main analysis on patterns of weekdays and at 40 years of age, because weekdays are more representative of daily lifestyle habits, and this also helped avoid having missing data on weekend patterns. We used data at 40 years of age to avoid potential reverse causation since it has been reported that cancer can cause anorexia (loss of appetite), thus affecting eating patterns [25].
Clinical information on prostate cancer aggressiveness determined by the Gleason score was recorded from medical records. We did not use the new Gleason grading system because of small numbers in some groups [26]. We classified cases into two groups: low-grade aggressive prostate cancer (Gleason score = 6 or 3 + 4) and high-grade aggressive prostate cancer (Gleason score 4 + 3 or higher), as it has been previously reported in the literature [27].
2.4. Statistical Analyses
We compared the distribution of characteristics in prostate cancer cases and controls and also prostate cancer risk factors according to nighttime fasting duration in controls. To evaluate significant differences, chi-square tests and t-tests were applied to calculate the p-value in categorical and continuous variables, respectively.
We assessed the correlation between nighttime fasting and the other dietary circadian variables (time of supper, interval between supper and sleep and time of breakfast) using Spearman’s correlation coefficient. We examined the linearity of the association between nighttime fasting duration (continuous variable, in hours) and prostate cancer using generalized additive models (GAM). We applied ANOVA, including the smoothing terms versus the linear term model, to test this association’s linearity.
Odds ratios (OR) and 95% confidence intervals (CI) were estimated with unconditional logistic regression using categorical exposure data. The crude model was adjusted for age (continuous, years), center (Madrid, Barcelona, Asturias, Huelva, Cantabria, Valencia, Granada) and for educational level (less than primary school, primary school, secondary school, university). We included educational level in the crude model because population controls had a higher level of education compared to cases [22]. Moreover, in our study population, education was significantly associated both with the exposure and the outcome (see Table 1 and Table 2).
Since there is limited prior evidence of determinants for both the exposure and the outcome, we followed a mixed criterion for the selection of further potential confounders. First, on the basis of the limited prior knowledge, we built a directed acyclic graph using Daggity (Figure S1) [28]. The variables considered were family history of prostate cancer (yes, no), adherence to a healthy lifestyle through the WCRF/AICR score (high, medium, low), indoor ALAN (total darkness, almost dark, dim light, quite illuminated), outdoor ALAN (continuous, cd/m2), sleep problems (yes, no) and duration (7 h or less, more than 7 h), number of daily eating episodes (three or less, more than three), time of the last intake (before 9 PM, 9:00 to <10 PM, 10 PM, or later) and the interval between the time of supper and sleep (1 h or less, from >1 to 2 h, more than 2 h). “Time of breakfast” was categorized in two levels (8:30 AM or before, after 8:30 or skip breakfast). Skipping breakfast has been associated with negative metabolic outcomes, but in our study only 3 cases reported never having breakfast. We also considered timing of physical activity (inactive, 8 AM–10 AM, 10 AM–12 PM, 12 PM–7 PM, 7 PM–11 PM, any other pattern), since it has been recently reported that morning exercise may be associated with a lower risk of prostate cancer compared to exercising later in the day [29]. Additionally, we considered diabetes (yes, no) because its treatment can include changes in dietary habits and it has been inconsistently suggested as a protective factor for prostate cancer [30,31,32]. Finally, we included BMI (continuous, kg/m2), smoking (never, ex-smoker, current smoker) and chronotype (morning, intermediate, evening).
In the adjusted model we included variables strongly associated with both the exposure and outcome in our study population (see Table 1 and Table 2) and variables changing the association between nighttime fasting and prostate cancer risk by more than 10% (Table S1). These variables were diabetes and indoor ALAN for the first criterion and breakfast time as the second criterion. Less than 1% of data was missing in the selected covariates. Multicollinearity was assessed in the adjusted model through the variance inflation factor to control for redundancy.
We explored whether there was evidence of effect modification of the association of interest by chronotype, healthy lifestyle (assessed with the WCRF/AICR score) and time of breakfast, including an interaction term in each of the models and examining results from a likelihood ratio test. We also investigated the combined association of nighttime fasting duration and time of breakfast with prostate cancer risk. The association between nighttime fasting and prostate cancer aggressiveness was examined with a multinomial logistic regression model. The statistical package R-4.0.0 (The R Project for Statistical Computing, Vienna, Austria) was used for these analyses.
2.5. Sensitivity Analyses
We explored the role of nighttime fasting on days off and working days by combining nighttime fasting data from weekdays and weekends (at 40 years of age). We used a weighted mean giving a weight of 5/7 to weekdays and of 2/7 to weekends. We also explored eliminating point outliers of the exposure distribution to exclude the most extreme patterns. We considered as potential point outliers any observation below the Q1 − (1.5*IQR) and above Q3 + (1.5*IQR). Nine (0.6%) and 35 observations (2.4%) were identified and excluded, respectively. To test the robustness of our results, exposure the previous year to the circadian interview was also considered, despite the potential bias due to reverse causation. This model was adjusted for time of breakfast corresponding to the year before the circadian interview and we assumed that exposure to indoor ALAN did not change during these years.
The time elapsed between the inclusion in the study and the exposure assessment from the circadian interview was long for some participants. Therefore, we did a sensitivity analysis including only those participants that answered the interview 3 years or less after the baseline questionnaire.
3. Results
3.1. Study Population
Characteristics of the included prostate cancer cases (N = 607) and matched controls (N = 848) are shown in Table 1. Educational level (p-value < 0.001), family history of prostate cancer (p-value < 0.001) and poor adherence to the WCRF/AICR recommendations (p-value = 0.004) were significantly associated with prostate cancer. Having a shorter time interval elapsed between supper and sleep (p-value = 0.034), not having breakfast consistently (p-value = 0.001) and being exposed to indoor artificial light at night (p-value = 0.001) were significantly associated with prostate cancer. Cases were less likely to have diabetes (p-value = 0.003).
3.2. Nighttime Fasting and Prostate Cancer Risk
The median nighttime fasting duration in the control group was 11 h (interquartile range 10–12). The distribution among controls of prostate cancer risk factors according to categories of nighttime fasting duration is presented in Table 2. Highly educated subjects tended to fast fewer hours overnight (p-value < 0.001). Participants with diabetes and less exposed to indoor ALAN tended to have more extended nighttime fasting periods (p-value = 0.052 and 0.005, respectively). Participants who never had breakfast or had the first intake after 8:30 AM and the last intake before 9 PM tended to fast for more hours (p-value < 0.001 for both variables).
A low positive correlation was observed between nighttime fasting duration and time elapsed between supper and sleep (Figure S2A, with a Spearman’s correlation coefficient of 0.12). Time of supper and nighttime fasting duration showed a low negative correlation (Figure S2B, with a Spearman’s correlation coefficient of −0.36). High correlation was found between nighttime fasting duration and time of breakfast (Figure S2C, Spearman’s correlation coefficient of 0.83).
The GAM showed a slight reduction of prostate cancer risk with more extended nighttime fasting (Figure S3A). When adjusting this model for time of breakfast, the reduction in the prostate cancer risk associated with fasting was more evident (Figure S3B). In the crude logistic regression model, fasting for more than 11 h overnight was associated with a slightly non-significant reduced risk of prostate cancer compared to those fasting for 11 h or less (OR = 0.92, 95% CI 0.73–1.16, Table 3). After adjusting for confounders, the model showed that a more extended nightly fast was linked to a more potent reduction of prostate cancer risk (adjusted model, OR = 0.77, 95% CI 0.54–1.07, Table 3). In this model, having breakfast after 8:30 AM was associated with a non-significant increased risk of prostate cancer (OR = 1.30, 95% CI 0.92–1.85) compared to having breakfast at 8:30 AM or before. We did not find important collinearity in the adjusted model between the two diet time-related variables.
We also tried categorizing the exposure into three categories based on the distribution of this variable in the control group: 10 h or less (reference category), more than 10 h to 12 h, and more than 12 h (Table S2). In this analysis, fasting for more than 10 h to 12 h was associated with a slightly higher prostate cancer reduced risk than the most extended fasting category. This difference was dissipated when adjusting for time of breakfast, suggesting that this difference could be explained by the adverse effects of postponing breakfast.
3.3. Prostate Cancer Risk Stratified by Time of First Intake
The prostate cancer risk reduction with a prolonged nightly fast was moderately stronger among those individuals having their breakfast at 8:30 or before (adjusted model, OR = 0.60, 95% CI 0.33–1.04) compared to those having it later on the day or skipping it (OR = 0.90, 95% CI 0.58–1.39, Table 4). Despite this pattern, confidence intervals overlapped and the interaction in the adjusted model was not significant (p-value = 0.26, 1 degree of freedom).
3.4. Association Combining Nighttime Fasting Duration and Time of Breakfast with Prostate Cancer Risk
When combining both nighttime fasting duration and time of breakfast we observed that the combination associated with a lower risk of prostate cancer was having a long nighttime fasting and an early breakfast compared to a short nighttime fasting and a late breakfast (OR = 0.54, 95% CI 0.27–1.04, Table 5). This association was maintained even after adjusting for time of last intake and interval between supper and sleep.
3.5. Prostate Cancer Risk Stratified by Chronotype
The association of prolonged fasting period overnight and reduced prostate cancer risk was slightly more pronounced in morning chronotype individuals (adjusted model, OR = 0.70, 95% CI 0.47–1.04) compared to intermediate and particularly evening ones (OR= 0.80, 95% CI 0.50–1.27; OR = 0.99, 95% CI 0.51–1.92, Table 6). However, the likelihood ratio test for interaction in the adjusted model showed a p-value = 0.60 with 2 degrees of freedom. On the other hand, we observed no effect modification by adherence to the WCRF/AICR score (Table S3).
3.6. Relative Risk among Cancer Subtypes
We evaluated the association between fasting overnight and aggressiveness of prostate cancer (Gleason score) in a multinomial logistic regression model. The association of prolonged fasting overnight and reduced prostate cancer risk was similar in cases diagnosed with a more aggressive prostate cancer subtype (Gleason score of 4 + 3 or higher) and in those with a Gleason score of 6 or 3 + 4 (adjusted model, OR = 0.78, 95% CI 0.53–1.14 and OR = 0.71, 95% CI 0.42–1.19, Table 7). The differences among cancer subtypes were non-significant (p-value = 0.97).
3.7. Sensitivity Analyses
Further adjustment of the model with other potential confounders did not change the estimates (Table S1). Combining data from weekdays and weekends did not result in different estimates than on weekdays only (data not shown). Removing the outliers of the exposure variable distribution also had a minimal effect on estimates (adjusted model, OR = 0.76, 95% CI 0.54–1.06, Table S4). The GAM in this reduced dataset showed the same pattern (see Figure S3C,D).
The median nighttime fasting duration reported one year before the inclusion in the study in the control group was 11.50 h (interquartile range 10.50–12.50). Models built with data on nighttime fasting during weekdays reported one year before diagnosis or before inclusion in the study for the controls changed the direction of the association (adjusted model OR = 1.13, 95% CI 0.88–1.46, Table S5). Analyzing the cancer subtypes, we observed that the relative risk ratio for aggressive prostate cancer cases (adjusted RRR = 1.23, 95% CI 0.82–1.84, Table S6) was slightly higher than for less aggressive cases (adjusted RRR = 1.10, 95% CI 0.83–1.46, Table S6).
In a model that excluded participants answering the circadian interview more than 3 years later from the baseline interview strengthened the findings (participants interviewed within 3 years: OR = 0.68, 95% CI 0.41–1.13; all participants: OR = 0.77, 95% CI 0.54–1.07).
4. Discussion
This is one of the first studies to examine the association between nighttime fasting duration and cancer risk. These findings suggest a possible lower risk of prostate cancer with longer overnight fasting time, especially when feeding is synchronized with the appropriate circadian timing by having an early breakfast.
From an evolutionary perspective, the benefits of a prolonged period of fast overnight are plausible. Life on earth has evolved to adapt and anticipate daily environmental oscillations resulting from the 24 h rotation of our planet. Natural selection drove the development of circadian rhythms enabling the daily optimization of energy acquisition, including sunlight (for photosynthetic organisms) or food [33]. The circadian clock permitted organisms to be prepared and aroused to access food when available and store supplies and undergo repairment processes during fasting hours, improving metabolic fitness and survival [33]. The extensive discussion on the benefits of nighttime fasting in mass media (e.g., Twitter) that are frequently based on this evolutionary perspective is not, however, backed by reliable population data.
Prolonged periods of fast overnight have been linked to a significant improvement in glycemic control and inflammation biomarkers, potentially explaining a lower risk of prostate cancer [18,19]. Our results are consistent with those of the prospective WHEL study, showing that fasting for less than 13 h was associated with a 36% increased hazard of breast cancer recurrence than a more extended fasting period [20]. Similarly to what we found, the prospective study from the NutriNet-Santé cohort showed that each hour increase in time of first intake was associated with a 17% increase in the hazard of developing PCa (HR = 1.17, 95% CI 0.96–1.43) [12]. However, contrary to what we found, even adjusting for this confounding effect of time of breakfast, nighttime fasting duration was associated with a slight increase in the hazard of developing prostate cancer in this study population (HR= 1.12, 95% CI 0.93–1.34) [12]. Differences between findings of epidemiological studies might be explained because of varying methods, sample sizes and time intervals examined.
It has been previously reported that time of supper [12,13] and time elapsed between supper and sleep [13] are associated with breast and prostate cancer. To disentangle these effects from the effects of nighttime fasting, we inspected their correlation and we explored adjustment of the crude model for these variables. We found low correlation between nighttime fasting duration and time of supper and with time interval between supper and sleep. Similarly, when we explored adjusting our basic model for time of last intake and for time interval between supper and sleep, the estimates did not significantly change. These results show that the potentially protective association between a prolonged nightly fasting period and reduced prostate cancer risk might be complementary to the protective association of having a larger time interval between supper and sleep.
Fasting regimens that promote long periods of fasting overnight, even by skipping breakfast, have become increasingly popular. Our results suggest that the time of breakfast is confounding the association between nighttime fasting and prostate cancer risk and that elongating the nightly period of fast by skipping breakfast might be counterproductive. Nighttime fasting is most beneficial when the eating window starts early in the morning, a form of intermittent fasting known as early time-restricted feeding [34]. Time-of-day variations in the benefits of nightly fasting can be explained by fluctuations of the circadian rhythms, which can also vary across chronotypes. The optimal time for food intake might be in the early hours of the day when diet-induced thermogenesis, glucose tolerance, insulin sensitivity, pancreatic beta-cell responsiveness and oxidation of fatty acids are higher [35].
Our study shows that in morning chronotype individuals, the association between a prolonged period overnight and a prostate cancer risk reduction is slightly larger than other chronotypes. This association was independent of the time of the first intake. On the contrary, in evening chronotype individuals, long nighttime fasting was not associated with lower prostate cancer risk. This may be explained by a higher frequency of chronic sleep deprivation and social jet-lag among late chronotypes, especially when working on early morning work schedules [36].
Reverse causation might explain the differences observed between the analyses of habits at 40 years of age and those shortly before disease or inclusion in the study. A possible explanation may be that eating and sleep habits one year before diagnosis might be reflecting a cancer-related loss of appetite or other early disease-related changes in lifestyle [25].
The strengths of this research include the novelty of the research question, the large sample size, the adjustment for a wide variety of well-measured confounders and the validated questionnaires to assess diet and the individual chronotype. As limitations, one of the primary concerns is that this assessment is subject to recall bias [13]. We tried to minimize this bias by requesting data on the timing of diet at mid-life. Additionally, in a sensitivity analysis, we explored excluding those participants with a longer time elapsed between inclusion in the study and exposure assessment in the circadian interview and, therefore, more prone to recall bias. After excluding these participants, estimates for our association of interest were strengthened. Meal timings and diet quality were assessed in one time point and these are behaviors prone to fluctuations. Future studies should include multiple time assessments to increase the validity of the results. A further inherent limitation of studies on prostate cancer is the lack of knowledge of this cancer’s non-genetic risk factors that could result in uncontrolled confounding. Finally, circadian patterns, including sleep timing and duration, light exposure and meal timings, are all interconnected. To improve public health recommendations, a future approach could be to analyze these behaviors in an integrated manner.
5. Conclusions
To conclude, this is one of the first studies with epidemiological data examining the association between nighttime fasting duration and prostate cancer risk and to consider the time window of this period of fasting. Complementing the previous results from the MCC study that showed a beneficial association between an early supper and a long supper–sleep time interval, our results suggest that lengthening the fasting period could be associated with a lower risk of this cancer, especially when having an early breakfast. This research highlights the importance of considering a circadian perspective, such as the time window of nighttime fasting and combined effects of meal timing aspects, in studies evaluating dietary and sleep determinants of cancer.
Supplementary Materials
The following are available online at https://www.mdpi.com/article/10.3390/nu13082662/s1. Figure S1. Directed acyclic graph representing the potential association between nighttime fasting duration and prostate cancer risk; Figure S2. Scatter plot for each of the correlations among controls; Figure S3. Generalized additive model examining the linearity of the association between nighttime fasting duration (continuous variable, in hours) and prostate cancer risk; Table S1. Examination of further adjustment with potential confounders; Table S2. Association of nighttime fasting duration with prostate cancer risk. Exposure variable categorized into three levels based on the distribution of this variable in the control group; Table S3. Association of nighttime fasting and prostate cancer risk stratified by adherence to the WCRF/AICR score; Table S4. Association of nighttime fasting duration with prostate cancer risk excluding outliers; Table S5. Association of nighttime fasting duration with prostate cancer risk based on information on dietary habits the year before the circadian interview; Table S6. Prostate cancer relative risk by cancer subtypes with information on dietary habits the year before the circadian interview.
Author Contributions
Conceptualization, A.P.-C., D.R., M.K., I.G.-A., J.A., G.F.-T., D.C.; Methodology, A.P.-C., A.E., K.S., K.P., G.C.-V., D.R., M.K.; Validation, R.O.-R., B.P.-G., A.M.-B.; Formal Analysis, A.P.-C., A.E.; Resources, J.A., G.F.-T., N.A., K.S., K.P.; Data Curation, A.E., G.C.-V.; Writing—Original Draft Preparation, A.P.-C., D.R., M.K.; Writing—Reviewing & Editing, A.P.-C., A.E., K.S., K.P., I.G.-A., B.P.-G., A.M.-B., R.O.-R., J.A., G.F.-T., D.C., N.A., G.C.-V., M.P., D.R., M.K.; Supervision, D.R., M.K.; Project Administration, G.C.-V., M.P., M.K.; Funding Acquisition, G.C.-V., M.P., M.K. All authors have read and agreed to the published version of the manuscript.
Funding
Instituto de Salud Carlos III FIS PI11/01889. Anna Palomar-Cros is supported by a MINECO (Ministry of Economy in Spain) fellowship. We acknowledge support from the Spanish State Research Agency and Ministry of Science and Innovation through the “Centro de Excelencia Severo Ochoa 2019–2023” Program (CEX2018-000806-S), and support from the Generalitat de Catalunya through the CERCA Program.
Institutional Review Board Statement
The study was conducted according to the guidelines of the Declaration of Helsinki, and approved by the Ethics committees of all participating institutions.
Informed Consent Statement
Informed consent was obtained from all subjects involved in the study.
Data Availability Statement
Data can be provided by contacting the corresponding author and following permission by the participating centres in the MCC Spain study. The computing code can be provided by the corresponding author.
Conflicts of Interest
The authors declare no conflict of interest.
References
- Sociedad Española de Oncología Médica (SEOM). Las Cifras del Cáncer en España. 2021. Available online: https://seom.org/images/Cifras_del_cancer_en_Espnaha_2021.pdf (accessed on 4 February 2021).
- Patel, A.R.; Klein, E.A. Risk factors for prostate cancer. Nat. Clin. Pr. Urol. 2009, 6, 87–95. [Google Scholar] [CrossRef]
- Ward, E.; Germolec, D.; Kogevinas, M.; McCormick, D.; Vermeulen, R.; Anisimov, V.; Aronson, K.; Bhatti, P.; Cocco, P.; Costa, G.; et al. Carcinogenicity of night shift work. Lancet Oncol. 2019, 20, 1058–1059. [Google Scholar] [CrossRef]
- Straif, K.; Baan, R.; Grosse, Y.; Secretan, B.; El Ghissassi, F.; Bouvard, V.; Altieri, A.; Benbrahim-Tallaa, L.; Cogliano, V.; WHO International Agency For Research on Cancer Monograph Working Group. Carcinogenicity of shift-work, painting, and fire-fighting. Lancet Oncol. 2007, 8, 1065–1066. [Google Scholar] [CrossRef]
- Challet, E. The circadian regulation of food intake. Nat. Rev. Endocrinol. 2019, 15, 393–405. [Google Scholar] [CrossRef]
- Garcia-Saenz, A.; Miguel, A.S. de Espinosa, A.; Valentin, A.; Aragonés, N.; Llorca, J.; Amiano, P.; Sánchez, V.M.; Guevara, M.; Capelo, R.; et al. Evaluating the Association between Artificial Light-at-Night Exposure and Breast and Prostate Cancer Risk in Spain (MCC-Spain Study). Environ. Health Perspect. 2018, 126, 47011. [Google Scholar] [CrossRef] [PubMed]
- Kim, K.Y.; Lee, E.; Kim, Y.J.; Kim, J. The association between artificial light at night and prostate cancer in Gwangju City and South Jeolla Province of South Korea. Chronobiol. Int. 2017, 34, 203–211. [Google Scholar] [CrossRef] [PubMed]
- Gapstur, S.M.; Diver, W.R.; Stevens, V.L.; Carter, B.D.; Teras, L.R.; Jacobs, E.J. Work schedule, sleep duration, insomnia, and risk of fatal prostate cancer. Am. J. Prev. Med. 2014, 46, S26–S33. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Sigurdardottir, L.G.; Markt, S.C.; Rider, J.R.; Haneuse, S.; Fall, K.; Schernhammer, E.S.; Tamimi, R.M.; Flynn-Evans, E.; Batista, J.L.; Launer, L.; et al. Urinary melatonin levels, sleep disruption, and risk of prostate cancer in elderly men. Eur. Urol. 2015, 67, 191–194. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Sigurdardottir, L.G.; Valdimarsdottir, U.A.; Mucci, L.A.; Fall, K.; Rider, J.R.; Schernhammer, E.; Czeisler, C.A.; Launer, L.; Harris, T.; Stampfer, M.J.; et al. Sleep disruption among older men and risk of prostate cancer. Cancer Epidemiol. Biomark. Prev. 2013, 22, 872–879. [Google Scholar] [CrossRef] [Green Version]
- Zhu, Y.; Zheng, T.; Stevens, R.G.; Zhang, Y.; Boyle, P. Does “clock” matter in prostate cancer? Cancer Epidemiol. Biomark. Prev. 2006, 15, 3–5. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Srour, B.; Plancoulaine, S.; Andreeva, V.A.; Fassier, P.; Julia, C.; Galan, P.; Hercberg, S.; Deschasaux, M.; Latino-Martel, P.; Touvier, M. Circadian nutritional behaviours and cancer risk: New insights from the NutriNet-santé prospective cohort study: Disclaimers. Int. J. Cancer 2018, 143, 2369–2379. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Kogevinas, M.; Espinosa, A.; Castelló, A.; Gómez-Acebo, I.; Guevara, M.; Martin, V.; Amiano, P.; Alguacil, J.; Peiro, R.; Moreno, V.; et al. Effect of mistimed eating patterns on breast and prostate cancer risk (MCC-Spain Study). Int. J. Cancer 2018, 143, 2380–2389. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Liu, X.; Zheng, C.; Xu, C.; Liu, Q.; Wang, J.; Hong, Y.; Zhao, P. Nighttime snacking is associated with risk of obesity and hyperglycemia in adults: A cross-sectional survey from Chinese adult teachers. J. Biomed. Res. 2017, 31, 541–547. [Google Scholar]
- Continuous Update Project: Diet, Nutrition, Physical Activity and the Prevention of Cancer. Summary of Strong Evidence. 2018. Available online: https://www.wcrf.org/wp-content/uploads/2021/02/Summary-of-Third-Expert-Report-2018.pdf (accessed on 10 March 2021).
- Lauby-Secretan, B.; Scoccianti, C.; Loomis, D.; Grosse, Y.; Bianchini, F.; Straif, K. Body Fatness and Cancer—Viewpoint of the IARC Working Group. N. Engl. J. Med. 2016, 375, 794–798. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Kesztyüs, D.; Cermak, P.; Gulich, M.; Kesztyüs, T. Adherence to Time-Restricted Feeding and Impact on Abdominal Obesity in Primary Care Patients: Results of a Pilot Study in a Pre-Post Design. Nutrients 2019, 11, 2854. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Marinac, C.R.; Natarajan, L.; Sears, D.D.; Gallo, L.C.; Hartman, S.J.; Arredondo, E.; Patterson, R.E. Prolonged Nightly Fasting and Breast Cancer Risk: Findings from NHANES (2009–2010). Cancer Epidemiol. Biomark. Prev. 2015, 24, 783–789. [Google Scholar] [CrossRef] [Green Version]
- Marinac, C.R.; Sears, D.D.; Natarajan, L.; Gallo, L.C.; Breen, C.I.; Patterson, R.E. Frequency and Circadian Timing of Eating May Influence Biomarkers of Inflammation and Insulin Resistance Associated with Breast Cancer Risk. PLoS ONE 2015, 10, e0136240. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Marinac, C.R.; Nelson, S.H.; Breen, C.I.; Hartman, S.J.; Natarajan, L.; Pierce, J.P.; Flatt, S.W.; Sears, D.D.; Patterson, R.E. Prolonged Nightly Fasting and Breast Cancer Prognosis. JAMA Oncol. 2016, 2, 1049–1055. [Google Scholar] [CrossRef] [PubMed]
- Nas, A.; Mirza, N.; Hägele, F.; Kahlhöfer, J.; Keller, J.; Rising, R.; Kufer, T.A.; Bosy-Westphal, A. Impact of breakfast skipping compared with dinner skipping on regulation of energy balance and metabolic risk. Am. J. Clin. Nutr. 2017, 105, 1351–1361. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Castaño-Vinyals, G.; Aragonés, N.; Pérez-Gómez, B.; Martín, V.; Llorca, J.; Moreno, V.; Altzibar, J.M.; Ardanaz, E.; de Sanjosé, S.; Jiménez-Moleón, J.J.; et al. Population-based multicase-control study in common tumors in Spain (MCC-Spain): Rationale and study design. Gac. Sanit. 2015, 29, 308–315. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Moreiras, O.; Cabrera, L.; Cuadrado, C.; Carbajal, A. Tablas de Composición de Alimentos; Pirámide: Madrid, Spain, 2003. [Google Scholar]
- Romaguera, D.; Gracia-Lavedan, E.; Molinuevo, A.; de Batlle, J.; Mendez, M.; Moreno, V.; Vidal, C.; Castelló, A.; Pérez-Gómez, B.; Martín, V.; et al. Adherence to nutrition-based cancer prevention guidelines and breast, prostate and colorectal cancer risk in the MCC-Spain case-control study. Int. J. Cancer 2017, 141, 83–93. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Thomas, F.; Rome, S.; Mery, F.; Dawson, E.; Montagne, J.; Biro, P.A.; Beckmann, C.; Renaud, F.; Poulin, R.; Raymond, M.; et al. Changes in diet associated with cancer: An evolutionary perspective. Evol. Appl. 2017, 10, 651–657. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Epstein, J.I.; Egevad, L.; Amin, M.B.; Delahunt, B.; Srigley, J.R.; Humphrey, P.A. The 2014 International Society of Urological Pathology (ISUP) Consensus Conference on Gleason Grading of Prostatic Carcinoma: Definition of Grading Patterns and Proposal for a New Grading System. Am. J. Surg. Pathol. 2016, 40, 244–252. [Google Scholar] [CrossRef]
- Neuzillet, Y.; Raynaud, J.-P.; Dreyfus, J.-F.; Radulescu, C.; Rouanne, M.; Schneider, M.; Krish, S.; Rouprêt, M.; Drouin, S.J.; Comperat, E.; et al. Aggressiveness of Localized Prostate Cancer: The Key Value of Testosterone Deficiency Evaluated by Both Total and Bioavailable Testosterone: AndroCan Study Results. Horm. Cancer 2019, 10, 36–44. [Google Scholar] [CrossRef] [PubMed]
- Textor, J.; van der Zander, B.; Gilthorpe, M.S.; Liśkiewicz, M.; Ellison, G.T.H. Robust causal inference using directed acyclic graphs: The R package ‘dagitty’. Int. J. Epidemiol. 2017, 45, 1887–1894. [Google Scholar] [CrossRef] [Green Version]
- Weitzer, J.; Castaño-Vinyals, G.; Aragonés, N.; Gómez-Acebo, I.; Guevara, M.; Amiano, P.; Martín, V.; Molina-Barceló, A.; Alguacil, J.; Moreno, V.; et al. Effect of time of day of recreational and household physical activity on prostate and breast cancer risk (MCC-Spain study). Int. J. Cancer 2021, 148, 1360–1371. [Google Scholar] [CrossRef] [PubMed]
- De Nunzio, C.; Tubaro, A. Prostate cancer: Diabetes and prostate cancer--an open debate. Nat. Rev. Urol. 2013, 10, 12–14. [Google Scholar] [CrossRef] [PubMed]
- Kasper, J.S.; Giovannucci, E. A meta-analysis of diabetes mellitus and the risk of prostate cancer. Cancer Epidemiol. Biomark. Prev. 2006, 15, 2056–2062. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Xu, H.; Jiang, H.W.; Ding, G.X.; Zhang, H.; Zhang, L.M.; Mao, S.H.; Ding, Q. Diabetes mellitus and prostate cancer risk of different grade or stage: A systematic review and meta-analysis. Diabetes Res. Clin. Pr. 2013, 99, 241–249. [Google Scholar] [CrossRef]
- Patterson, R.E.; Laughlin, G.A.; LaCroix, A.Z.; Hartman, S.J.; Natarajan, L.; Senger, C.M.; Martínez, M.E.; Villaseñor, A.; Sears, D.D.; Marinac, C.R.; et al. Intermittent Fasting and Human Metabolic Health. J. Acad. Nutr. Diet. 2015, 115, 1203–1212. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Jamshed, H.; Beyl, R.A.; Della Manna, D.L.; Yang, E.S.; Ravussin, E.; Peterson, C.M. Early Time-Restricted Feeding Improves 24-Hour Glucose Levels and Affects Markers of the Circadian Clock, Aging, and Autophagy in Humans. Nutrients 2019, 11, 1234. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Queiroz, J.D.N.; Macedo, R.C.O.; Tinsley, G.M.; Reischak-Oliveira, A. Time-restricted eating and circadian rhythms: The biological clock is ticking. Crit. Rev. Food Sci. Nutr. 2020, 1–13. [Google Scholar] [CrossRef] [PubMed]
- Mazri, F.H.; Manaf, Z.A.; Shahar, S.; Mat Ludin, A.F. The Association between Chronotype and Dietary Pattern among Adults: A Scoping Review. Int. J. Environ. Res. Public Health 2019, 17, 68. [Google Scholar] [CrossRef] [PubMed] [Green Version]
Figure 1.
Flow chart of study population. N = sample size.
Table 1.
Basic characteristics of study population.
| Controls (N = 848) | Cases (N = 607) | p-Value | |
|---|---|---|---|
| Mean (SD) or N (%) | Mean (SD) or N (%) | ||
| Age | 66.0 (8.4) | 65.6 (7.0) | 0.372 |
| BMI | 27.5 (3.6) | 27.5 (3.6) | 0.967 |
| Normal weight (<25 kg/m2) | 225 (26.5) | 153 (25.2) | 0.850 |
| Overweight (≥25 to <30 kg/m2) | 439 (51.8) | 320 (52.7) | |
| Obese (≥30 kg/m2) | 184 (21.7) | 134 (22.1) | |
| Educational level | |||
| Less than primary school | 115 (13.6) | 104 (17.1) | <0.001 |
| Primary school | 247 (29.1) | 244 (40.2) | |
| Secondary school | 264 (31.1) | 142 (23.4) | |
| University | 222 (26.2) | 117 (19.3) | |
| Family history of prostate cancer | |||
| No | 793 (93.5) | 506 (83.4) | <0.001 |
| Yes | 55 (6.5) | 101 (16.6) | |
| Smoking | |||
| Never | 242 (28.5) | 171 (28.2) | 0.571 |
| Ex-smoker | 434 (51.2) | 325 (53.5) | |
| Current smoker | 172 (20.3) | 111 (18.3) | |
| Chronotype | |||
| Morning | 419 (50.5) | 306 (50.5) | 0.974 |
| Intermediate | 303 (36.6) | 224 (37.0) | |
| Evening | 107 (12.9) | 76 (12.5) | |
| Unknown | 19 | 1 | |
| WCRF/AICR score | |||
| Low adherence a | 307 (40.1) | 203 (37.3) | 0.004 |
| Medium adherence b | 262 (34.2) | 232 (42.6) | |
| High adherence c | 196 (25.6) | 109 (20.0) | |
| Unknown | 83 | 63 | |
| Diabetes | |||
| No | 671 (79.3) | 518 (85.6) | 0.003 |
| Yes | 175 (20.7) | 87 (14.4) | |
| Unknown | 2 | 2 | |
| Indoor ALAN exposure | |||
| Total darkness | 147 (17.4) | 87 (14.4) | 0.001 |
| Almost dark | 348 (41.2) | 211 (34.9) | |
| Dim light | 261 (30.9) | 204 (33.7) | |
| Quite illuminated | 88 (10.4) | 103 (17.0) | |
| Unknown | 4 | 2 | |
| Breakfast | |||
| No | 17 (2.0) | 3 (0.5) | 0.001 |
| Only weekends | 3 (0.4) | 12 (2.0) | |
| Only weekdays | 15 (1.8) | 16 (2.6) | |
| Always | 809 (95.9) | 575 (94.9) | |
| Unknown | 4 | 1 | |
| Time of breakfast | |||
| 8:30 AM or before | 466 (55.0) | 314 (51.7) | 0.227 |
| After 8:30 AM or skip breakfast | 382 (45.0) | 293 (48.3) | |
| Time of last intake | |||
| 10 PM or later | 294 (34.7) | 227 (37.4) | 0.350 |
| 9:00 to <10 PM | 439 (51.8) | 311 (51.2) | |
| Before 9 PM | 115 (13.6) | 69 (11.4) | |
| Supper/sleep interval | |||
| 1 h or less | 186 (22.2) | 169 (28.1) | 0.034 |
| From >1 to ≤2 h | 327 (39.0) | 223 (37.0) | |
| More than 2 h | 326 (38.9) | 210 (34.9) | |
| Unknown | 9 | 5 | |
ALAN = artificial light at night; BMI = body mass index; N = sample size; NA = not applicable; SD = standard deviation; WCRF/AICR = World Cancer Research Fund / American Institute for Cancer Research. a Men (0.25–3); Women (0.5–3.5). b Men (3.25–4); Women (3.75–4.25). c Men (4.25–6); Women (4.5–6).
Table 2.
Distribution of prostate cancer risk factors according to nighttime fasting duration in controls.
Table 2.
Distribution of prostate cancer risk factors according to nighttime fasting duration in controls.
| ≤11 h of Fast (N = 474) | >11 h of Fast (N = 374) | p-Value | |
|---|---|---|---|
| Mean (SD) or N (%) | Mean (SD) or N (%) | ||
| Age | 65.5 (8.5) | 66.5 (8.2) | 0.070 |
| BMI | 27.4 (3.5) | 27.6 (3.8) | 0.384 |
| Normal weight (<25 kg/m2) | 121 (25.5) | 104 (27.8) | 0.198 |
| Overweight (≥25 to <30 kg/m2) | 258 (54.4) | 181 (48.4) | |
| Obese (≥30 kg/m2) | 95 (20.0) | 89 (23.8) | |
| Educational level | |||
| Less than primary school | 50 (10.5) | 65 (17.4) | <0.001 |
| Primary school | 115 (24.3) | 132 (35.3) | |
| Secondary school | 161 (34.0) | 103 (27.5) | |
| University | 148 (31.2) | 74 (19.8) | |
| Family history of prostate cancer | |||
| No | 445 (93.9) | 348 (93.0) | 0.727 |
| Yes | 29 (6.1) | 26 (7.0) | |
| Smoking | |||
| Never | 140 (29.5) | 102 (27.3) | 0.191 |
| Ex-smoker | 230 (48.5) | 204 (54.5) | |
| Current smoker | 104 (21.9) | 68 (18.2) | |
| Chronotype | |||
| Morning | 219 (47.1) | 200 (54.9) | 0.080 |
| Intermediate | 181 (38.9) | 122 (33.5) | |
| Evening | 65 (14.0) | 42 (11.5) | |
| Unknown | 9 | 10 | |
| WCRF/AICR score | |||
| Low adherence a | 164 (38.2) | 143 (42.6) | 0.432 |
| Medium adherence b | 154 (35.9) | 108 (32.1) | |
| High adherence c | 111 (25.9) | 85 (25.3) | |
| Unknown | 45 | 38 | |
| Diabetes | |||
| No | 387 (81.8) | 284 (76.1) | 0.052 |
| Yes | 86 (18.2) | 89 (23.9) | |
| Unknown | 1 | 1 | |
| Indoor ALAN exposure | |||
| Total darkness | 63 (13.3) | 84 (22.6) | 0.005 |
| Almost dark | 203 (43.0 | 145 (39.0) | |
| Dim light | 151 (32.0) | 110 (29.6) | |
| Quite illuminated | 55 (11.7) | 33 (8.9) | |
| Unknown | 2 | 2 | |
| Breakfast | |||
| No | 1 (0.2) | 16 (4.3) | <0.001 |
| Only weekends | NA | 3 (0.8) | |
| Only weekdays | 8 (1.7) | 7 (1.9) | |
| Always | 465 (98.1) | 344 (93.0) | |
| Unknown | NA | 4 | |
| Time of breakfast | |||
| 8:30 AM or before | 417 (88.0) | 49 (13.1) | <0.001 |
| After 8:30 AM or skip breakfast | 57 (12.0) | 325 (86.9) | |
| Time of last intake | |||
| 10 PM or later | 215 (45.4) | 79 (21.1) | <0.001 |
| 9:00 to <10 PM | 233 (49.2) | 206 (55.1) | |
| Before 9 PM | 26 (5.5) | 89 (23.8) | |
| Supper/sleep interval | |||
| 1 h or less | 110 (23.6) | 76 (20.4) | 0.553 |
| From >1 to ≤2 h | 178 (38.1) | 149 (40.1) | |
| More than 2 h | 179 (38.3) | 147 (39.5) | |
| Unknown | 7 | 2 | |
ALAN = artificial light at night; BMI = body mass index; N = sample size; SD = standard deviation; WCRF/AICR = World Cancer Research Fund / American Institute for Cancer Research. a Men (0.25–3); Women (0.5–3.5). b Men (3.25–4); Women (3.75–4.25). c Men (4.25–6); Women (4.5–6).
Table 3.
Association of nighttime fasting and prostate cancer risk.
| Nighttime Fasting | Controls N (%) | Cases N (%) | OR (95% CI) a | OR (95% CI) b |
|---|---|---|---|---|
| ≤11 h | 474 (55.9) | 342 (56.3) | Ref | Ref |
| >11 h | 374 (44.1) | 265 (43.7) | 0.92 (0.73–1.16) | 0.77 (0.54–1.07) |
N = sample size; OR = odds ratio; 95% CI = 95% confidence interval. a Adjusted for age, center and education. b Adjusted for age, center, education, diabetes (missing for 2 controls and 2 cases), indoor ALAN exposure (missing for 4 controls and 2 cases) and time of breakfast.
Table 4.
Association of nighttime fasting and prostate cancer risk stratified by time of breakfast.
| Nighttime Fasting | Controls N (%) | Cases N (%) | OR (95% CI) a | OR (95% CI) b |
|---|---|---|---|---|
| Breakfast at 8:30 AM or before | ||||
| ≤11 h | 417 (89.5) | 293 (93.3) | Ref | Ref |
| >11 h | 49 (10.5) | 21 (6.7) | 0.66 (0.37–1.13) | 0.60 (0.33–1.04) |
| Breakfast after 8:30 AM or skip breakfast | ||||
| ≤11 h | 57 (14.9) | 49 (16.7) | Ref | Ref |
| >11 h | 325 (85.1) | 245 (83.3) | 0.87 (0.57–1.33) | 0.90 (0.58–1.39) |
N = sample size; OR = odds ratio; 95% CI = 95% confidence interval. a Adjusted for age, center and education. b Adjusted for age, center, education, diabetes (missing for 2 controls and 2 cases), indoor ALAN exposure (missing for 4 controls and 2 cases) and chronotype (missing for 19 controls and 1 case).
Table 5.
Association of nighttime fasting and time of breakfast with prostate cancer risk.
| Controls N (%) | Cases N (%) | OR (95% CI) a | OR (95% CI) b | |
|---|---|---|---|---|
| Short nighttime fasting (≤11 h) and late breakfast (>8:30 AM) | 56 (6.6) | 49 (8.1) | Ref | Ref |
| Short nighttime fasting (≤11 h) and early breakfast (≤8:30 AM) | 418 (49.3) | 293 (48.3) | 0.88 (0.57–1.36) | 0.89 (0.57–1.39) |
| Long nighttime fasting (>11 h) and late breakfast (>8:30 AM) | 325 (38.3) | 244 (40.2) | 0.87 (0.57–1.33) | 0.88 (0.57–1.36) |
| Long nighttime fasting (>11 h) and early breakfast (≤8:30 AM) | 49 (5.8) | 21 (3.5) | 0.58 (0.30–1.11) | 0.54 (0.27–1.04) |
N = sample size; OR = odds ratio; 95% CI = 95% confidence interval. a Adjusted for age, center and education. b Adjusted for age, center, education, diabetes (missing for 2 controls and 2 cases) and indoor ALAN exposure (missing for 4 controls and 2 cases).
Table 6.
Association of nighttime fasting and prostate cancer risk stratified by chronotype (missing for 19 controls and for 1 case).
Table 6.
Association of nighttime fasting and prostate cancer risk stratified by chronotype (missing for 19 controls and for 1 case).
| Nighttime Fasting | Controls N (%) | Cases N (%) | OR (95% CI) a | OR (95% CI) b |
|---|---|---|---|---|
| Morning chronotype | ||||
| ≤11 h | 219 (52.3) | 170 (55.5) | Ref | Ref |
| >11 h | 200 (47.7) | 136 (44.5) | 0.84 (0.61–1.15) | 0.70 (0.47–1.04) |
| Intermediate chronotype | ||||
| ≤11 h | 181 (59.7) | 130 (58.0) | Ref | Ref |
| >11 h | 122 (40.3) | 94 (42.0) | 0.97 (0.67–1.41) | 0.80 (0.50–1.27) |
| Evening chronotype | ||||
| ≤11 h | 65 (60.7) | 41 (53.9) | Ref | Ref |
| >11 h | 42 (39.3) | 35 (46.1) | 1.17 (0.63–2.18) | 0.99 (0.51–1.92) |
N = sample size; OR = odds ratio; 95% CI = 95% confidence interval. a Adjusted for age, center and education. b Adjusted for age, center, education, diabetes (missing for 2 controls and 2 cases), indoor ALAN exposure (missing for 4 controls and 2 cases) and time of first intake.
Table 7.
Association of nighttime fasting and prostate cancer relative risk by cancer subtypes (missing for 17 cases).
Table 7.
Association of nighttime fasting and prostate cancer relative risk by cancer subtypes (missing for 17 cases).
| Nighttime Fasting | Controls N (%) | Cases N (%) | RRR (95% CI) a | RRR (95% CI) b |
|---|---|---|---|---|
| Low aggressiveness | ||||
| ≤11 h | 474 (55.9) | 246 (56.7) | Ref | Ref |
| >11 h | 374 (44.1) | 188 (43.3) | 0.91 (0.71–1.18) | 0.78 (0.53–1.14) |
| High aggressiveness | ||||
| ≤11 h | 474 (55.9) | 86 (55.1) | Ref | Ref |
| >11 h | 374 (44.1) | 70 (44.9) | 0.92 (0.63–1.33) | 0.71 (0.42–1.19) |
N = sample size; RRR = Relative risk ratio; 95% CI = 95% confidence interval. a Adjusted for age, center and education. b Adjusted for age, center, education, diabetes (missing for 2 controls and 2 cases), indoor ALAN exposure (missing for 4 controls and 2 cases) and time of first intake.
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Palomar-Cros, A.; Espinosa, A.; Straif, K.; Pérez-Gómez, B.; Papantoniou, K.; Gómez-Acebo, I.; Molina-Barceló, A.; Olmedo-Requena, R.; Alguacil, J.; Fernández-Tardón, G.; et al. The Association of Nighttime Fasting Duration and Prostate Cancer Risk: Results from the Multicase-Control (MCC) Study in Spain. Nutrients 2021, 13, 2662. https://doi.org/10.3390/nu13082662
AMA Style
Palomar-Cros A, Espinosa A, Straif K, Pérez-Gómez B, Papantoniou K, Gómez-Acebo I, Molina-Barceló A, Olmedo-Requena R, Alguacil J, Fernández-Tardón G, et al. The Association of Nighttime Fasting Duration and Prostate Cancer Risk: Results from the Multicase-Control (MCC) Study in Spain. Nutrients. 2021; 13(8):2662. https://doi.org/10.3390/nu13082662
Chicago/Turabian StylePalomar-Cros, Anna, Ana Espinosa, Kurt Straif, Beatriz Pérez-Gómez, Kyriaki Papantoniou, Inés Gómez-Acebo, Ana Molina-Barceló, Rocío Olmedo-Requena, Juan Alguacil, Guillermo Fernández-Tardón, and et al. 2021. "The Association of Nighttime Fasting Duration and Prostate Cancer Risk: Results from the Multicase-Control (MCC) Study in Spain" Nutrients 13, no. 8: 2662. https://doi.org/10.3390/nu13082662
APA StylePalomar-Cros, A., Espinosa, A., Straif, K., Pérez-Gómez, B., Papantoniou, K., Gómez-Acebo, I., Molina-Barceló, A., Olmedo-Requena, R., Alguacil, J., Fernández-Tardón, G., Casabonne, D., Aragonés, N., Castaño-Vinyals, G., Pollán, M., Romaguera, D., & Kogevinas, M. (2021). The Association of Nighttime Fasting Duration and Prostate Cancer Risk: Results from the Multicase-Control (MCC) Study in Spain. Nutrients, 13(8), 2662. https://doi.org/10.3390/nu13082662
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