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Article

Altered Red Blood Cell Fatty Acid and Serum Adipokine Profiles in Subjects with Obesity

by
Asier Léniz
1,2,3,4,5,6,
Alfredo Fernández-Quintela
2,3,4,5,6,*,
Sara Arranz
7,
Kevin Portune
7,
Itziar Tueros
7,
Eunate Arana
8,
Luis Castaño
8,9,10,11,12,
Olaia Velasco
8,9,10,11,12 and
María P. Portillo
2,3,4,5,6
1
Vitoria-Gasteiz Nursing School, Osakidetza-Basque Health Service, 01009 Vitoria-Gasteiz, Spain
2
BIOARABA Institute of Health, 01006 Vitoria-Gasteiz, Spain
3
CIBER Physiopathology of Obesity and Nutrition (CIBERobn), Institute of Health Carlos III, 01006 Vitoria-Gasteiz, Spain
4
Nutrition and Obesity Group, Department of Nutrition and Food Sciences, Faculty of Pharmacy, University of the Basque Country (UPV/EHU), Paseo de la Universidad, 7, 01006 Vitoria-Gasteiz, Spain
5
Lucio Lascaray Research Centre, Avenida Miguel de Unamuno, 3, 01006 Vitoria-Gasteiz, Spain
6
Department Pharmacy and Food Sciences, Faculty of Pharmacy, University of the Basque Country (UPV/EHU), 01006 Vitoria-Gasteiz, Spain
7
AZTI, Food Research, Basque Research and Technology Alliance (BRTA), Parque Tecnológico de Bizkaia, Astondo Bidea, Edificio 609, 48160 Derio, Spain
8
Hospital Universitario Cruces, BIOBIZKAIA Institute of Health, 48903 Barakaldo, Spain
9
Department Pediatrics, Faculty of Medicine and Nursing, University of the Basque Country (UPV/EHU), 48940 Leioa, Spain
10
CIBER Diabetes and Associated Metabolic Diseases (CIBERdem), Institute of Health Carlos III, 48903 Barakaldo, Spain
11
CIBER Rare Diseases (CIBERer), Institute of Health Carlos III, 48903 Barakaldo, Spain
12
European Reference Network on Rare Endocrine Conditions (ENDO-ERN), 48903 Barakaldo, Spain
 
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*
Author to whom correspondence should be addressed.
Biomedicines 2023, 11(12), 3320; https://doi.org/10.3390/biomedicines11123320
Submission received: 21 November 2023 / Revised: 13 December 2023 / Accepted: 14 December 2023 / Published: 15 December 2023
(This article belongs to the Special Issue Recent Advances in Adipokines—2nd Edition)
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Abstract

:
Background: Adipokines, as well as the fatty acid profile of red blood cell (RBC) membranes, are known to play important roles in the development and progression of metabolic complications induced by obesity. Thus, the objective of this study is to compare the serum adipokine profile and the RBC membrane fatty acid profile of normal-weight and obese adults, and to analyze their relationship with serum biochemical parameters. Methods: An observational case–control study was performed in 75 normal-weight and obese adult subjects. Biochemical serum parameters, eight serum adipokines and the RBC membrane fatty acid profiles were measured. Associations between parameters were established using regression analysis. Results: Subjects with obesity showed increased levels of leptin, fibroblast growth factor 21 (FGF21) and overexpressed nephroblastoma (NOV/CCN3), decreased adiponectin, and similar levels of vaspin and chemerin compared to normal-weight subjects. Significant positive and negative correlations were found with triglycerides and high-density lipoprotein-cholesterol (HDL-c), respectively. An increase in the total ω-6 fatty acids in the RBC membrane fatty acid profiles in subjects with obesity was observed, because of higher levels of both dihomo-γ-linolenic acid (DGLA) and arachidonic acid (AA), and decreased total ω-3 fatty acids, mainly due to lower levels of docosahexaenoic acid (DHA). The ω-6/ω-3 ratio in the RBCs was significantly higher, suggesting an inflammatory status, as was also suggested by a reduced adiponectin level. A negative association between DGLA and adiponectin, and a positive association between DHA and serum triglycerides, was observed. Conclusions: Important alterations in serum adipokine and RBC fatty acid profiles are found in subjects with obesity.

1. Introduction

Obesity can be defined as an excessive accumulation of fat mass with consequential effects on health. Nowadays, obesity has become a relevant health problem worldwide, especially in Western countries, and it affects almost 30% of the world population [1]. This disease is a key factor in the development of metabolic syndromes, and it can induce alterations at the inflammatory and hormonal level. As a result, obesity is associated with a variety of co-morbidities such as type 2 diabetes, dyslipidemia, hypertension, arthritis, non-alcoholic fatty liver diseases, breathing pathologies and some types of cancer [2].
Cytokines are 5 to 30 kDa peptides, glycoproteins or proteins secreted by cells that act, via receptors, to regulate the growth, responsiveness or maturation of certain target cell groups. Once a cytokine binds to its corresponding receptor in the cell surface, an intracellular signaling cascade is triggered, which leads to changes in gene expression of the target cell and, consequently, to a biological action. Cytokines can regulate complex networks with autocrine, paracrine or endocrine functions and can act in a pleiotropic, redundant, synergic or antagonistic manner [3].
Among cytokines, great attention has been paid to those secreted by white adipose tissue, known as adipocytokines or adipokines. Adipose tissue is considered an endocrine organ that can establish a crosstalk with other organs and tissues by secreting adipokines. These molecules play important roles in regulating whole-body homeostasis with a relevant influence in the development and progression of metabolic complications induced by obesity [4,5]. In the presence of adipocyte hypertrophy produced by excess energy storage, adipokine secretion is altered due to an energy imbalance, which contributes to the pathogenesis of obesity-associated complications [6].
On the other hand, the fatty acid profile of red blood cell (RBC) membranes can be considered a good predictor of the fatty acid profile of other body tissues [7], and can help monitor the ω-6 and ω-3 fatty acid contents in phospholipids that are directly linked with inflammation mediators. Additionally, since RBC half-life is around 4 months, membrane fatty acid composition of these cells can reflect the status of obesity-related diseases [8].
The aim of the present study is to compare the serum adipokine profile and the RBC membrane fatty acid profiles of normal-weight and obese adults, and to analyze their relationship with serum biochemical parameters.

2. Materials and Methods

2.1. Design and Subjects

The present observational case–control study was carried out on a cohort of 37 normal-weight (18 males and 19 females) and 38 obese (19 males and 19 females) 19–68 year-old adult subjects recruited from the Endocrinology Department at the Hospital Universitario Cruces (Barakaldo, Spain). The distribution between both groups was made according to body mass index (BMI), taking BMI > 30 kg/m2 as a reference to classify obesity and 18.5 < BMI < 25 kg/m2 for the normal-weight group. After a physical examination by an endocrinologist, participants with any kind of acute or chronic disease or who were taking medication were excluded from the study. Anthropometric measurements were all conducted by doctors during the participant’s visit to the Hospital Universitario Cruces/IIS Biocruces Bizkaia.
The study protocol was approved by the Euskadi Clinical Research Ethics Committee (permission number PI2016181) and carried out according to the ethics principles derived from the Declaration of Helsinki, consistent with Good Clinical Practice guidelines. All participants were provided with a written informed consent form, in agreement with the corresponding laws (Organic Law 3/2018, of December 5, Protection of Personal Data and guarantee of digital rights; Law 14/2007 on Biomedical Research and RD 1716/2011 of Biobanks).

2.2. Blood Collection and Biochemical Analysis

Blood samples were obtained in vacutainer tubes containing ethylenediaminetetraacetic acid (EDTA). Blood was centrifuged at 1250× g for 20 min, and the plasma obtained was stored at −80 °C until analysis. Plasma concentrations of glucose, insulin, total cholesterol (TC), high-density lipoprotein cholesterol (HDL-c), low-density lipoprotein cholesterol (LDL-c), triglycerides (TG), aspartate aminotransferase (AST), alanine aminotransferase (ALT), uric acid and bilirubin were measured using standard laboratory assays.
For cytokine measurements, sensitive and specific enzyme-linked immunoassay kits were used: RD191001100 (BioVendor, Brno, Czech Republic) for leptin, RD195023100 (BioVendor, Brno, Czech Republic) for adiponectin, RD191100200R (BioVendor, Brno, Czech Republic) for omentin, ab155430 (Abcam, Cambridge, UK) for chemerin, RD191097200R (BioVendor, Brno, Czech Republic) for vaspin, ab193710 (Abcam, Cambridge, UK) for NOV-CCN3, ab222506 (Abcam, Cambridge, UK) for FGF21 and RD191016100 (BioVendor, Brno, Czech Republic) for resistin. The measurements were performed with a Labsystems iEMS Reader MF analyzer plate photometer (Labsystems Diagnostics Oy, Helsinki, Finland).
The homeostatic model assessment for insulin resistance (HOMA-IR) was calculated using the following formula:
HOMA-IR = Fasting plasma insulin (μU/mL) × fasting glycaemia (mg/d μU L)/405

2.3. Red Blood Cell (RBC) Membrane Fatty Acid Analysis

The fatty acid composition of mature RBC membrane phospholipids was obtained from blood samples (approximately 2 mL) collected in vacutainer tubes containing ethylenediaminetetraacetic acid (EDTA). Samples were shipped to the Lipidomic Laboratory, where they underwent the certified procedure MEM_LIP_1 upon arrival, according to the quality control guidelines. The absence of hemolysis was promptly checked. For the blood, the procedure to extract and work-up lipids to obtain fatty acid methyl esters (FAMEs) was conducted following an automated protocol, including the selection of mature RBCs as previously disclosed [8,9]. Briefly, the EDTA blood was centrifuged (4000 rpm for 5 min at 4 °C) and the cell fraction was isolated based on the high density of the aged cells and controlled using a cell counter (Scepter 2.0 with Scepter™ Software Pro, EMD Millipore, Darmstadt, Germany). The automated equipment subsequently executed the following tasks: cell lysis, membrane pellets isolation, and phospholipid extraction from pellets using the Bligh and Dyer method [10], transesterification to FAMEs was made with a solution of methyl alcohol and potassium hydroxide (0.5 mol/L) during 10 min at room temperature and extracted using n-hexane (2 mL). The automated procedure is available at the Lipidomic Laboratory facility of Lipinutragen srl (www.lipinutragen.it) and is compliant with the ISO/EIC 17025:2017 regulation [11]. Laboratory machinery used to analyze FAMEs were a capillary column gas chromatography Agilent 6850 Network, supplied with a fused silica capillary column Agilent DB23 (60 m × 0.25 mm × 0.25 µm) and a flame ionization detector (FID). Libraries of trans isomers of monounsaturated (MUFAs) and polyunsaturated fatty acids (PUFAs) [12] and commercial standards allow us to separate and identify fatty acids as well as their geometrical and positional isomers registered. The results are reported as a relative % for each fatty acid, with more than 97% of the GC peaks recognized with appropriate standards.

2.4. Statistical Analysis

Data are presented as mean values ± standard error of the mean. The statistical analyses were performed using IBM SPSS statistics (v25, Chicago, IL, USA). Normal data distribution were assessed with Shapiro–Wilk’s test and the Kolmogorov–Smirnov test. Differences between groups (subjects with a normal weight and subjects with obesity) were evaluated using Student’s t test or the Mann–Whitney U test for data that were not normally distributed. Correlations between variables were conducted using Spearman’s rank correlation. Multiple linear regression analysis was used to find the major determinants for serum biochemical parameters. This stepwise regression was achieved by including all potential independent variables in the model and eliminating those that were not statistically significant using a backward selection method. Statistical significance was chosen at p value of <0.05.

3. Results

3.1. Anthropometric Parameters

As expected, obese subjects presented higher values of BMI and waist circumference (Table 1).

3.2. Biochemical Parameters

Table 2 summarizes the biochemical parameters of normal-weight subjects and subjects with obesity. The latter presented higher concentrations of glucose, insulin, uric acid, LDL-cholesterol, triglycerides and alanine aminotransferase (ALT/GPT) than normal-weight subjects, as well as lower levels of HDL-cholesterol and albumin. No significant differences were found in total cholesterol and aspartate aminotransferase (AST/GOT). The HOMA-IR index was significantly higher in subjects with obesity.

3.3. Adipokine Concentrations

Figure 1 shows adipokine concentrations. Subjects with obesity showed significantly higher values of NOV/CCN3, leptin and FGF21, and significantly lower values of adiponectin than normal-weight subjects. No significant differences were found in omentin, vaspin and chemerin. Lastly, resistin showed a tendency towards higher values in subjects with obesity than in individuals with normal weight.

3.4. Fatty Acid Profile of RBCs

Table 3 shows the fatty acid profile of RBCs. No significant differences were observed in saturated fatty acids between both groups. Although individual monounsaturated fatty acids (MUFAs) were not different between groups, subjects with obesity showed significantly lower levels of total MUFAs. The fatty acid that contributed the most to this difference was sapienic acid (C16:1, 6c). The ratio of saturated/monounsaturated fatty acid (SFAs/MUFAs) was significantly higher in obese subjects compared to normal-weight subjects, mainly due to the lower level of MUFAs. Subjects with obesity also showed a significantly lower level of total ω-3 fatty acids, caused for the most part by the lower level of docosahexaenoic acid (DHA), and an increased level of total ω-6 fatty acids which was largely induced by the increase in dihomo-γ-linolenic acid (DGLA) and arachidonic acid (AA). Consequently, the ratio ω-6/ω-3 was significantly higher in individuals with obesity than in normal-weight subjects.
Based on the ratios between specific fatty acids, the activity of delta-5 desaturase (∆5D), delta-9 desaturase (∆9D) and delta-6 desaturase (∆6D) + elongase (ELO) was estimated. Whereas a nonsignificant difference was observed in the activity of ∆9D, that of ∆5D was higher in subjects with obesity and ∆6D + ELO was lower in subjects with obesity.

3.5. Correlation Analysis

The correlations between serum metabolic parameters and cytokines, using only cytokine data that showed significant differences between non-obese subjects and individuals with obesity, are shown in Table 4. Positive correlations are as follows: Serum glucose, insulin and HOMA-IR with leptin and FGF21; Serum triglycerides with leptin; HDL-c with adiponectin and FGF21; Uric acid with FGF21; ALT/GPT with FGF21. In contrast, Serum glucose, insulin and HOMA-IR, serum triglycerides, uric acid, and ALT/GPT all correlated negatively with adiponectin.
Lastly, Table 5 shows the correlations between cytokines and RBCs fatty acid profiles. Adiponectin was positively correlated with ∆6D + ELO and ∆5D, and negatively correlated with DGLA. Negative correlations were observed between leptin, ∆6D + ELO and DHA and total ω-3 fatty acids, and a positive correlation between this adipokine and the ratio ω-6/ω-3. FGF21 was positively correlated with DGLA and negatively with ∆6D + ELO.

3.6. Stepwise Multiple Regression Analysis for Major Determinations

This analysis was performed to find a set of independent variables that significantly influence biochemical parameters, adipokines and RBC membrane fatty acid. The independent variables included in the multiple regression analysis were participant sex, age and BMI, for all dependent variables, the parameters that showed to be correlated with each dependent factor through backward stepwise selection. The results are shown in Table 6.

4. Discussion

Cytokines can represent interesting biomarkers of metabolic disorders and diseases. In the present study the cytokine profile of subjects with obesity that showed metabolic syndrome, in agreement with the US National Cholesterol Education Programme Adult Treatment Panel III (NCEP ATP III) [13], was evaluated and compared with that of healthy normal-weight subjects. Subjects with obesity showed an altered serum cytokine profile, characterized by increased levels of leptin, FGF21 and NOV/CCN3, a decreased level of adiponectin, and similar levels of vaspin and chemerin compared to normal-weight subjects. In general terms, this altered profile can be related to an increased risk of suffering alterations in glycemic control and inflammation [5,14]. The alterations in adipokine levels in subjects with obesity have been widely studied. However, in the vast majority of studies either a single adipokine or a reduced number of adipokines has been analyzed. Thus, a strength of the present research is that concurrent levels of eight adipokines have been studied in the same cohort together with the association with other metabolic parameters such as RBC fatty acids and biochemistry.
Correlation analyses showed a positive association between leptin and three classical parameters related to glycemic control, serum glucose, serum insulin and HOMA-IR index, and negative correlations between each of these parameters and adiponectin or FGF21. The correlations between leptin or adiponectin and glycemic control-related parameters have been widely described [15,16,17,18,19], and the present results are in accordance with the published works. Few clinical studies examining the effects of FGF21 on glycemic control and obesity are available. In the present work, increased serum FGF21 levels showed a positive correlation with glycemic control-related parameters. Nevertheless, the multiple regression analysis did not show any association between this adipokine and the glycemic control-related parameters.
In general, FGF21 influences glucose homeostasis by stimulating glucose uptake by adipocytes and inhibiting glucose production in the liver or improving insulin sensitivity [20]. In accordance with our results, other authors observed higher serum FGF21 levels in subjects with obesity compared to those detected in lean individuals [21,22]. However, a recent meta-analysis revealed that the use of FGF21 analogs exhibited no effect on fasting blood glucose, glycated hemoglobin, and HOMA index, although a decreased fasting insulinemia was detected. As stated by the authors, the quality of the evidence ranged from moderate to very low and more clinical trials are needed to increase the quality of this evidence [23].
Regarding serum lipids, the correlation study showed significant correlations with adiponectin, leptin and FGF21. The regression analysis confirmed the positive association between FGF21 and triglycerides and a negative correlation between FGF21 and HDL-cholesterol, which is in line with that observed by other authors [24,25,26]. It has been shown that this cytokine increases the expression of PGC1-α in the liver, which induces FFA oxidation through mitochondrial enhancement, thus preventing their conversion into triglycerides and reducing serum triglyceride concentration. Moreover, FGF21 lowers serum triglyceride levels through the suppression of white adipose tissue lipolysis, lipoprotein lipase activity increase and thus lipoprotein clearance enhancement [27]. Taking these facts into account, a resistance to FGF21 can be proposed [28,29]. Regarding, HDL-cholesterol, it has been demonstrated that FGF21 inhibits the expression of SREBP-2 [30], and that this transcription factor activates the transcription of the hepatic enzyme ABCA1, which catalyzes the assembly of cholesterol, phospholipids and apoproteins for HDL-c secretion from liver [31]. Consequently, FGF21 reduces HDL-cholesterol production. Moreover, a negative association between adiponectin and serum triglycerides, and a positive association between adiponectin and HDL-cholesterol were also confirmed by the regression analysis. These results are in accordance with those reported by other authors [32,33]. With regard to the negative association between adiponectin and serum triglycerides, it has been proposed that adiponectin increases triglycerides clearance by increasing lipoprotein lipase expression in white adipose tissue [34]. The positive association between adiponectin and HDL-cholesterol can be explained because compelling evidence suggests that adiponectin plays a significant role in promoting cellular cholesterol efflux and HDL biogenesis. Indeed, it has been hypothesized that ABCA1 activity and adiponectin receptors, AdipoR1 and AdipoR2, play a critical role in adiponectin-mediated cholesterol efflux [35].
In addition, adiponectin was negatively correlated with uric acid. Other studies in the literature have also shown this correlation in cohorts with characteristics different from those of the present study, in terms of ethnic background, age or gender [36,37,38]. However, the multiple regression analysis did not confirm the association.
Although it is known that transaminases are not as good markers of liver damage as imagined, ALT is the most commonly used parameter to reflect hepatic impairment, including non-alcoholic fatty liver disease (NAFLD). Other authors reported a positive correlation between ALT and FGF21 [39,40]. Moreover, several studies have shown that plasma FGF21 concentration was highly correlated with hepatic fat content in cases of mild and moderate liver steatosis, either in adult subjects [41,42,43,44] or children [45,46,47,48]. Unfortunately, once again the multiple regression analysis did not confirm the association. In contrast, regression analysis showed a positive association between leptin and the ratio ALT/AST. Taking into account that leptin increases in overweight subjects and subjects with obesity, this association could suggest the development of fatty liver in the subjects with obesity in the present study. Nevertheless, this hypothesis could not be confirmed because, unfortunately, potential liver steatosis was not analyzed in these subjects.
To summarize, the main result concerning the relationship between serum biochemical parameters and serum cytokines are the significant associations found between FGF21 and adiponectin with serum lipids (triglycerides and HDL-cholesterol).
With regard to the fatty acid profile in RBC membranes, in subjects with obesity this was characterized by an increase in total ω-6 fatty acids, as a result of a higher level of DGLA, and a decrease in total ω-3 fatty acids, mainly due to a lower level of DHA. Consequently, the ratio ω-6/ω-3 was significantly higher. The increase in ω-6 fatty acids and the decrease in ω-3 fatty acids observed in subjects with obesity, when compared with normal-weight subjects, indicated that the former showed an inflammatory status, as was also suggested by a reduced adiponectin level.
Concerning DGLA, several authors have proposed that the increased level of this fatty acid observed in obesity may represent a mechanism conferring protective effects against the associated inflammation [49,50]. This is due to its conversion into the series-1 prostanoids via the cyclooxygenase pathway and suppression of inflammatory leukotriene (LT) formation, and the ability to compete with AA in the synthesis of pro-inflammatory AA mediators [51,52]. However, other studies have reported a positive association with inflammatory and endothelial activation markers, with a more significant association found in obese adults [53]. In fact, DGLA can be converted to 15-HETrE via the 15-lipoxygenase pathway [54]. Regression analysis revealed a negative association between DGLA and adiponectin, suggesting that the increase in DGLA in RBC membranes acts as an inflammatory marker [51].
On the other hand, DHA, an ω-3 polyunsaturated fatty acid with cardioprotective effects was negatively associated with leptin. In fact, low levels of ω-3 fatty acids and high levels of leptin have been reported in subjects with obesity, which are related to a proinflammatory state [55]. A recent systematic review revealed that an increase in DHA intake can negatively modulate the expression of leptin [56]. Taking into account that RBC fatty profiles reflect in part fatty acid intake, this result might be in line with the association found in the present study.
The association between serum triglycerides and the content of DGLA in RBC has been scarcely studied. The present results do not agree with those reported by Deon et al., who did not find any significant association, but it should be noted that their study was addressed in children and adolescents with primary hyperlipidemia [57].
In addition, adiponectin was positively correlated with ∆6D + ELO and the association was maintained after the adjustment in the multiple regression analysis. There are few studies showing this association in the literature; they have been addressed, not in RBC membrane phospholipids, but in plasma phospholipids [58,59]. Nevertheless, taking into account that plasma phospholipids do not mirror RBC membrane phospholipids [60,61], no comparisons with the present results can be made.
In conclusion, important alterations in serum adipokine profile and RBC fatty acid profiles are found in subjects with obesity. Regression analysis reveals interesting associations between adipokines and other biochemical serum parameters, between RBC fatty acid profiles and general biochemical serum parameters, and between serum adipokines and RBC fatty acid profile, some of them being described for the first time. In view of these associations, further studies are needed to better explain them, and to check if they are also found in other cohorts.
The present study shows some limitations, the relatively small number of subjects in the sample being one of them. This fact may have affected the strength of the correlations found in this cohort. Another limitation is that, due to the cross-sectional nature of the study, it is not possible to determine a cause-and-effect relationship between changes in adipokine and RBC fatty acid profiles and the alterations found in the serum biochemical parameters in the obese subjects. Moreover, diet is considered to be the major modifying factor of fatty acid composition of tissues. Unfortunately, dietary intake was not registered in the present study.

Author Contributions

A.F.-Q., S.A., M.P.P. and L.C. designed the study; A.L. and I.T. conducted the study; A.L., S.A., K.P., I.T., E.A. and O.V. collected and analyzed data; A.F.-Q., A.L., S.A. and M.P.P. wrote the initial draft of the manuscript; M.P.P. and S.A., funding acquisition, M.P.P., O.V. and L.C. and A.F.-Q.; supervision. All authors contributed to the editing and review of this manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Department of Environment: Territorial Planning: Agriculture and Fisheries of the Basque Country Government (OBINTER project funding by ELKARTEK 2019 KK-2019/00028; Innovation Fund 2017), the Department of Education of the Basque Country Government (IT1482-22) and CIBEROBN under Grant CB12/03/30007.

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki and approved by the Euskadi Clinical Research Ethics Committee (permission number PI2016181).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

The data that support the findings of this study are available from the corresponding author, upon reasonable request.

Conflicts of Interest

The authors declare no conflict of interest.

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Biomedicines 11 03320 g001
Figure 1. Adipokine concentrations in normal-weight subjects and subjects with obesity. Data are expressed as mean ± SEM. * Statistically different from the normal-weight group.
Figure 1. Adipokine concentrations in normal-weight subjects and subjects with obesity. Data are expressed as mean ± SEM. * Statistically different from the normal-weight group.
Biomedicines 11 03320 g001
Table 1. Anthropometric parameters in normal-weight subjects and subjects with obesity.
Table 1. Anthropometric parameters in normal-weight subjects and subjects with obesity.
Normal-Weight Subjects
(n = 37)		Subjects with Obesity (n = 38)
Weight (kg)66.9 ± 1.4111.6 ± 5.0 ***
Height (cm)170.4 ± 1.7166.9 ± 1.60
BMI (kg/m2)22.9 ± 0.240.8 ± 1.1 ***
Waist circumference (cm)78.7 ± 1.6120.0 ± 2.6 ***
Data are expressed as mean ± SEM. *** p < 0.001. BMI: body mass index.
Table 2. Biochemical parameters in normal-weight and obese subjects.
Table 2. Biochemical parameters in normal-weight and obese subjects.
Normal-Weight Subjects
(n = 37)		Subjects with Obesity
(n = 38)
Glucose (mg/dL)86.9 ± 1.50103.0 ± 3.2 **
Insulin (mU/L)10.0 ± 1.120.5 ± 1.9 **
HOMA-IR2.2 ± 0.25.6 ± 0.5 **
Total cholesterol (mg/dL)184.8 ± 6.6193.4 ± 5.3
HDL-c (mg/dL)61.3 ± 2.650.5 ± 2.7 **
LDL-c (mg/dL)107.1 ± 5.3121.9 ± 4.9 *
Triglycerides (mg/dL)80.72 ± 4.9155.5 ± 11.2 **
AST/GOT (U/L)19.3 ± 0.821.7 ± 1.3
ALT/GPT (U/L)19.5 ± 1.726.3 ± 1.9 *
AST/ALT1.2 ± 0.10.9 ± 0.04 **
Data are expressed as mean ± SEM. * p < 0.05; ** p < 0.01. ALT/GPT: Alanine transaminase; AST/GOT: Aspartate aminotransferase; HDL-c: high-density lipoprotein cholesterol; HOMA-IR: homeostasis model of assessment of insulin resistance; LDL-c: low-density lipoprotein cholesterol.
Table 3. Red blood cell (RBC) membrane fatty acid profile in normal-weight subjects and subjects with obesity.
Table 3. Red blood cell (RBC) membrane fatty acid profile in normal-weight subjects and subjects with obesity.
Fatty Acid (%)Normal-Weight
Subjects (n = 37)		Subjects with Obesity
(n = 38)
Palmitic acid (C16:0)22.13 ± 0.2722.66 ± 0.19
Stearic acid (C18:0)17.12 ± 0.2317.11 ± 0.19
Total SFAs39.25 ± 0.2939.77 ± 0.22
Sapienic acid (C16:1, 6c)0.38 ± 0.030.32 ± 0.04
Palmitoleic acid (C16:1, 9c)0.48 ± 0.030.45 ± 0.03
Oleic acid (C18:1, 9c)17.04 ± 0.1916.75 ± 0.22
cis-Vaccenic acid (C18:1, 11c)1.29 ± 0.051.24 ± 0.04
Total MUFAs19.19 ± 0.2118.76 ± 0.23
Linoleic acid (C18:2)12.82 ± 0.2012.43 ± 0.29
Alpha-linolenic acid (C18:3)0.22 ± 0.020.20 ± 0.02
Dihomo-γ-linolenic acid (C20:3)1.84 ± 0.092.19 ± 0.07 **
Arachidonic acid (C20:4)18.03 ± 0.3318.89 ± 0.31
Eicosapentaenoic acid (C20:5)0.73 ± 0.080.64 ± 0.06
Docosapentaenoic acid (C22:5)1.97 ± 0.071.82 ± 0.05
Docosahexaenoic acid (C22:6)5.75 ± 0.205.12 ± 0.22 *
Total ω-632.69 ± 0.4633.50 ± 0.40
Total ω-38.67 ± 0.297.80 ± 0.30 *
Total PUFA41.36 ± 0.4241.30 ± 0.31
Trans C18:10.09 ± 0.010.10 ± 0.01
Trans C20:4 0.11 ± 0.020.08 ± 0.01
Total Trans0.20 ± 0.020.18 ± 0.02
SFA/MUFA2.05 ± 0.022.13 ± 0.03 *
ω-6/ω-33.95 ± 0.164.56 ± 0.20 *
∆6D + ELO 20:3/18:20.15 ± 0.010.18 ± 0.01 *
∆5D 20:4/20:310.47 ± 0.458.98 ± 0.35 *
∆9D 16:1/16:058.88 ± 6.1264.49 ± 6.12
∆9D 18:1/18:01.01 ± 0.021.03 ± 0.02
Data are presented as mean ± standard error of the mean. * p < 0.05; ** p <0.01. D: desaturase; ELO: elongase; MUFA: monounsaturated fatty acid; PUFA: polyunsaturated fatty acid; SFA: saturated fatty acid.
Table 4. Correlations between serum cytokines and biochemical parameters.
Table 4. Correlations between serum cytokines and biochemical parameters.
AdiponectinNOV/CCN3LeptinFGF21
Glucoseρ−0.338 **0.1460.453 **0.356 **
p0.0040.2440.0000.002
Insulinρ−0.392 **0.0610.495 **0.451 **
p0.0010.6150.0000.000
HOMA-IRρ−0.441 **0.0790.504 **0.503 **
p0.0000.5130.0000.000
Triglyceridesρ−0.434 **0.2230.395 **0.546 **
p0.0000.0660.0010.000
Cholesterolρ0.1440.1190.1760.123
p0.2210.3250.1330.295
HDL-cρ0.441 **−0.062−0.179−0.389 **
p0.0000.6240.1420.001
LDL-cρ0.0270.2130.1980.229
p0.8310.0940.1090.063
Uric acid ρ−0.360 **0.1740.1960.313 **
p0.0020.1500.0950.007
ALT/ASTρ−0.353 **0.0120.0270.265 *
p0.0030.9230.8210.026
ρ: Spearman’s correlation coefficient; p: p-value. * p < 0.05; ** p < 0.01. Significant correlations are in bold. ALT: Alanine transaminase; AST: Aspartate aminotransferase; HDL-c: high-density lipoprotein cholesterol; HOMA-IR: homeostasis model of assessment of insulin resistance; LDL-c: low-density lipoprotein cholesterol.
Table 5. Correlations between fatty acids in RBC membranes and cytokines.
Table 5. Correlations between fatty acids in RBC membranes and cytokines.
AdiponectinLeptinFGF21
∆6D + ELOρ0.412 **−0.344 *−0.322 *
p0.0040.0240.042
∆5Dρ0.374 *−0.197−0.263
p0.0110.3010.121
DGLAρ−0.378 *0.0680.337 *
p0.0110.2970.029
DHAρ0.177−0.375 *−0.131
p0.3640.0110.531
total ω-3 fatty acidsρ0.122−0.393 **−0.168
p0.5730.0060.398
ω-6/ω-3 ratioρ−0.1240.345 *0.157
p0.5620.0240.435
Ρ: Spearman’s correlation coefficient; p: p-value. * p < 0.05; ** p < 0.01. Significant correlations are in bold.; D: desaturase; DGLA: dihomo-γ-linolenic acid; DHA: docosahexaenoic acid; ELO: elongase.
Table 6. Stepwise multiple regression analysis.
Table 6. Stepwise multiple regression analysis.
Dependent VariableIndependent Variablesβ CoefficientpAdjusted R2
HOMA-IRsex−0.2510.0400.362
adiponectin−0.2730.017
leptin0.5210.000
TriglyceridesFGF210.4760.0000.329
adiponectin−0.2770.007
HDL-cFGF21−0.2720.0170.207
adiponectin0.3600.002
Uric acidage0.2670.0120.236
sex−0.4200.000
ALTsex−0.5530.0000.296
AdiponectinHOMA-IR−0.3200.0050.352
sex0.3070.004
D6D + ELO0.3150.005
LeptinHOMA-IR0.1750.0450.876
age0.1750.009
sex0.5200.000
ALT/AST0.1280.021
DHA−0.1750.000
FGF21triglycerides0.3290.0030.339
age0.3300.003
HDL-cholesterol−0.2320.029
DGLAtriglycerides0.3120.0150.187
adiponectin−0.2530.047
Δ6D + ELOadiponectin0.3210.0080.283
leptin−0.4260.001
Δ5Dtriglycerides−0.4100.0000.156
HDL-c: high-density lipoprotein cholesterol; HOMA-IR: homeostasis model of assessment of insulin resistance; ALT: Alanine transaminase; AST: Aspartate aminotransferase; DHA: Docosahexaenoic acid; D: desaturase; DGLA: Dihomo-γ-linolenic acid; ELO: elongase; FGF21: fibroblast growth factor 21. Sex variables considered as 0 for males and 1 for females.
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Léniz, A.; Fernández-Quintela, A.; Arranz, S.; Portune, K.; Tueros, I.; Arana, E.; Castaño, L.; Velasco, O.; Portillo, M.P. Altered Red Blood Cell Fatty Acid and Serum Adipokine Profiles in Subjects with Obesity. Biomedicines 2023, 11, 3320. https://doi.org/10.3390/biomedicines11123320

AMA Style

Léniz A, Fernández-Quintela A, Arranz S, Portune K, Tueros I, Arana E, Castaño L, Velasco O, Portillo MP. Altered Red Blood Cell Fatty Acid and Serum Adipokine Profiles in Subjects with Obesity. Biomedicines. 2023; 11(12):3320. https://doi.org/10.3390/biomedicines11123320

Chicago/Turabian Style

Léniz, Asier, Alfredo Fernández-Quintela, Sara Arranz, Kevin Portune, Itziar Tueros, Eunate Arana, Luis Castaño, Olaia Velasco, and María P. Portillo. 2023. "Altered Red Blood Cell Fatty Acid and Serum Adipokine Profiles in Subjects with Obesity" Biomedicines 11, no. 12: 3320. https://doi.org/10.3390/biomedicines11123320

APA Style

Léniz, A., Fernández-Quintela, A., Arranz, S., Portune, K., Tueros, I., Arana, E., Castaño, L., Velasco, O., & Portillo, M. P. (2023). Altered Red Blood Cell Fatty Acid and Serum Adipokine Profiles in Subjects with Obesity. Biomedicines, 11(12), 3320. https://doi.org/10.3390/biomedicines11123320

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