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Article

Adaptation and Validation of a Questionnaire to Evaluate Knowledge of the Low Phe Diet in PKU

by
Rodolfo Ramos-Álvarez
1,*,
Maili Kapp
2,
María Mercedes Rodríguez-Ruiz
3,
Rocío Fausor
4,
María Amor Bueno-Delgado
5,
Kirsten Ahring
6 and
Susan E. Waisbren
7,*
1
Department of Social Psychology, Melilla Campus, Granada University, 52005 Melilla, Spain
2
Teaching Innovation Project (Code: 14–82), Melilla Campus, Granada University, 52005 Melilla, Spain
3
Osakidetza, Basque Health Service, 010006 Vitoria, Spain
4
Department of Personality, Assessment and Clinical Psychology, Complutense University of Madrid, 28223 Madrid, Spain
5
Pediatrics Service, Virgen del Rocío University Hospital, 41013 Sevilla, Spain
6
Center for PKU, Copenhagen University Hospital, 2600 Copenhagen, Denmark
7
Genetics and Metabolism Programs, Boston Children’s Hospital, Harvard Medical School, Harvard University, Boston, MA 02115, USA
*
Authors to whom correspondence should be addressed.
Nutrients 2021, 13(8), 2719; https://doi.org/10.3390/nu13082719
Submission received: 15 June 2021 / Revised: 21 July 2021 / Accepted: 30 July 2021 / Published: 7 August 2021
(This article belongs to the Section Nutrition Methodology & Assessment)
Versions Notes

Abstract

:
Phenylketonuria (PKU) is an autosomal recessive disorder of phenylalanine (Phe) metabolism, causing a build-up of Phe in the body. Treatment consists of a Phe-restricted diet for life and regular determination of blood Phe levels to monitor the intake of Phe. Despite the fact that diet is the cornerstone of treatment, there are no studies examining common knowledge about food items and whether they are allowed as part of the PKU diet. Improving parents’ and patients’ knowledge and competence about the diet enables them to make appropriate food choices. This study validates a food-knowledge questionnaire first developed in Spanish and modified for English speaking populations. The questionnaire potentially helps parents to prepare appropriate meals and healthcare providers to create individualized educational programs about PKU for children and adolescents with this disorder.

1. Introduction

Phenylketonuria (PKU), or phenylalanine hydroxylase deficiency (PAH deficiency), is an autosomal recessive disorder of phenylalanine (Phe) metabolism caused by a deficiency of the enzyme phenylalanine hydroxylase (PAH). Phe is one of the essential amino acids found in all protein. The inability to convert Phe to tyrosine causes the accumulation of Phe in the body. Excess Phe is toxic to the central nervous system [1,2]. The prevalence varies between countries. It is estimated to be 1:4000 in Turkey, 1:10,000 in Europe and between 1 in 10,000 to 15,000 in children born in the United States [3,4].
Before treatment, three phenotypes are differentiated based on blood Phe concentrations measured prior to initiating treatment. (1) In classic or severe PKU, Phe values exceed 1200 µmol/L. Untreated severe PKU leads to permanent intellectual disability, seizures, developmental delay, behavioral problems, and psychiatric disorders [5,6]. (2) In mild PKU, blood Phe concentrations are between 600–1200 µmol/L. Most centers now recommend dietary treatment and/or treatment with sapropterin dihydrochloride (BH4) for infants and children with blood Phe levels within this range. BH4 is a co-factor of the deficient enzyme and when supplemented is often effective in reducing blood Phe concentrations in mild PKU. (3) Mild hyperphenylalaninemia, with blood Phe concentrations 120–600 µmol/L, may not require dietary treatment [4,7,8].
There is consensus on the importance of controlling Phe in the blood, as measured through restricting dietary Phe [7,9]. Adherence to diet has been shown to be a reliable predictor of clinical outcomes. Frequent blood tests are required to assess metabolic status and determine an adequate dietary intake of Phe. In order to meet the body’s requirements for protein, individuals with PKU are prescribed a protein substitute with all the necessary nutrients and amino acids in protein apart from the “offending” amino acid, Phe. It also contains the amounts of fat, carbohydrate and micronutrients suitable or right for patients of a particular age. They consume this protein substitute, called a medical food, at least three times a day. It prevents the deficiency that may result from a limited intake of other amino acids and variable amounts of carbohydrates, fats, vitamins, and minerals [6,9,10].
Adhering to the Phe restricted diet for life is essential [10]. Initially, children with PKU will be guided by parents and later in adolescence and adulthood by self-management. This reduces the risks of cognitive decline in babies and mental and neurological problems in adults [11,12]. However, a low Phe diet during childhood but abandoned later in life can increase the risk of other adverse outcomes, such as depression, anxiety and executive functioning deficits in adulthood [13].
During adolescence and adulthood, many individuals with PKU find that the limited diet is unpleasant, difficult to follow and a hindrance to social relationships [14,15]. Studies show that PKU diet adherence decreases with age [16,17,18] and many patients are lost to follow-up [19]. Many factors can influence eating behavior. Different studies have considered demographic factors [20,21,22], educational level [23], environmental factors [15], nutritional knowledge and parents’ attitudes [24,25] and psychosocial factors [21], among others.
Equally important is knowledge and competence about diet, enabling the correct food choices [24,25,26]. Parents and individuals with PKU need to understand the age-appropriate nutrition recommendations as well as food-based guidelines, and how to apply these to food choices and eating behaviors [27,28].
Witalis and colleagues reported that only 33 to 40% of patients with PKU (10–19 years and >20 years) knew the Phe content in the most common food products [29]. Other authors have found that the parents’ poor dietary knowledge may have an impact on long-term metabolic control in children [30]. Some authors observe a negative correlation between maternal knowledge about food and the average concentration of Phe in the blood in the child [31]. In the general population, consumers from different countries vary in their level of knowledge about nutrition [27].
The early detection of misinformation and knowledge gaps among parents and patients would alert caregivers to provide training and to focus education on specific areas needed to improve motivation, dietary management, and adherence to medical recommendations [19,32].
Despite the fact that diet is the cornerstone of treatment, there are no objective measures of knowledge in English related to the allowed and disallowed foods in PKU.
The objective of this study was to adapt a Phe diet questionnaire, originally developed in Spain, for individuals with PKU and their parents. The questionnaire was translated into English and modified to incorporate foods commonly found in the United States (USA). Caregivers and individuals with PKU in the USA completed the questionnaire, representing the first of this kind to be administered by healthcare professionals.

2. Methods

2.1. Description of the Spanish Questionnaire

The Spanish questionnaire “Cuestionario de valoración de conocimientos sobre la dieta baja en fenilalanina en familiares de afectados por la fenilcetonuria” (Questionnaire to evaluate knowledge of the low Phe diet in PKU) provided the template for the questionnaire developed for the English speaking population in the USA. For the Spanish version, a representative sample of items taken from a list of all food types was chosen. Food selection for this representative sample was based on the following criteria or guidelines:
  • The amount of Phe in a food determined whether it was prohibited or allowed. The limit was set at 50 mg of Phe per 100 g product.
  • The proportion of prohibited and permitted foods included in the questionnaire was the same, with 34 items of permitted foods (42.5%) and 46 of prohibited foods or allowed only in very small quantities (57.5%).
  • All food categories were included: meat, fish, seafood, eggs, dairy, cereals, legumes, vegetables, fruits, beverages, sauces, sweets and condiments.
  • Within the different food categories, there were regularly consumed foods (prototypical) and less frequently consumed foods (non-prototypical).
  • All foods in the list were easily available and accessible for consumption.
The final Spanish version of the questionnaire included 80 items of food to be rated as “allowed” or “prohibited”. In addition, there were questions to elicit basic health and demographic information (age, sex, town of residence, level of education and type of phenylketonuria) and information about the person completing the questionnaire (age, sex, town of residence, level of education and relationship to the individual with PKU). The Spanish version of the questionnaire was found to be psychometrically sound, with a Cronbach’s index of 0.87. The Spanish version is available from the first author (R.R.-Á.) and a manuscript describing its development is forthcoming.

2.2. Translation and Adaptation of the Spanish Version to American Population

The Spanish questionnaire was translated into English and adapted to incorporate contemporary food practices and colloquial or common language. Guidelines proposed by Muñiz and Hambleton (1996) and Muñiz, Elosua and Hambleton (2013) were used [33,34]. After carrying out a morpho-semantic assessment, additional modifications about sociodemographic questions were made. Finally, items that presented comprehension problems were rewritten. A multinational and multidisciplinary panel of experts and consumers participated in the item selection phase to establish the questionnaire’s content validity. The panel included nutrition professionals, physicians, and other healthcare providers, as well as affected individuals and their parents recruited from the National PKU Alliance and the California PKU Association. In addition, a group of 6 native English speakers from outside of the PKU community, reviewed the questionnaire and provided suggestions regarding wording and item selection.
The questionnaire adaptation to American English revealed some differences related to expressions, the use of some foods and words to define them. For example, “Identification of the surveyed family member” was changed to “Data about the person who completes this survey.” Items related to education were also changed: “Nursery” became “kindergarten”; and “Number of years of education” replaced “Your level of education.” The most frequent changes related to food. For example, “Horchata” (a typical refreshing drink from an area of Spain) is almost unknown. The words “sweet potato” and “yam” led to confusion since the words are often used interchangeably in the USA, although referring to different species of tuberous vegetables. Lentils, commonly eaten in Europe, were not recommended until 2010 in the Dietary Guide for Americans and were dropped from the list. “Seasoning” replaced “vegetable concentrate” and “lobster” and “shrimp” were included instead of “prawns”.
Two versions of the questionnaire were made: a computer version and a paper version. Both versions were intended to be administered by a health professional but completed as a self-report questionnaire. Analyses revealed that both were assessing the same construct and that the data collection by the two different systems (paper and computer) did not affect the results. A forthcoming manuscript details the statistical methods used in the development of the questionnaire.
After initial piloting, additional terms were changed if found to be confusing, ambiguous or related to food items not in the diet. The final questionnaire (Supplementary Materials) included 80 items adapted to the American population. In addition, brief instructions were written. As the questionnaire involved simply placing a checkmark next to each food item, almost all participants completed the task in under 10 min, including completion of the sociodemographic questions.

2.3. Statistical Analyses

Once the translation was verified and content validity was determined, statistical analyses were performed to address psychometric properties of the questionnaire. A factor analysis was carried out with the Factor program (Tarragona, Spain) (Lorenzo-Seva and Ferrando, 2013) [35]. A tetrachoric correlation matrix, ULS fit and Promin rotation were used. Calculations were made for determining a non-normalized fit index (Tucker and Lewis, 1973) [36], a comparative fit index, a goodness of fit index and adjusted goodness of fit index. Details regarding the more extensive statistical methods to document the psychometric properties of the questionnaire will be included in a forthcoming manuscript.
Discrimination: item-total correlations were verified to identify the extent to which answering an item correctly was related to scoring high on the entire subscale. Items with Chronbach Alpha values below 0.30 would be eliminated.
Mean and variance: the questionnaire represents optimal performance (right/wrong responses). Therefore, items with extreme mean difficulty values (either too easy or too hard) were eliminated. Items with mean difficulty values close to 0.5 would be retained. Similarly, items that presented a very small variance, close to 0, would also be eliminated. Data were processed using IBM SPSS Statistics 25 software (Armonk, NY, USA). The level of statistical significance was set at p < 0.05.

2.4. Ethical Considerations

The research was carried out following recommended standards for research on human participants of the European Community Code of Ethics as well as Ethical Research and Publication Standards of the Psychological Association. The research was approved by the vice-rector for research of the UGR and the Melilla Campus, Granada University, Granada Spain, with the approval of the National PKU Alliance and the California PKU Association. Privacy in data processing was guaranteed. Participation in the study was voluntary and anonymous.

3. Results

3.1. Descriptive Analysis

The questionnaire was completed by 177 parents of children with PKU living in the USA. The mean age of the parents was 40.31 (SD = 8.66), with a range of 24–76 years. The mean age of their children (n = 177) was 6.92 (SD = 4.77) ranging from 1 to 18 years. The demographic data of the sample are presented in Table 1.
According to follow-up assessments by the respondents to both the on-line and paper versions, the questionnaire was clear and easy to understand. They described the instructions and the response options as simple and free of ambiguity. They reported that they had no difficulty in choosing the answers.

3.2. Psychometric Properties of the Subscales

  • Reliability analysis (internal consistency): global reliability was analyzed and confirmed. Without eliminating any of the final 80 items, Cronbach’s alpha coefficient was 0.945, indicating high internal reliability.
  • Factor analysis: as described below, a satisfactory 3-factor factorial solution was revealed by parallel analysis using Factor program (Lorenzo-Seva and Ferrando, 2013) [35].
    • Factor 1: foods allowed (factor reliability = 0.97).
    • Factor 2: prohibited foods, easy to recognize (factor reliability = 0.92).
    • Factor 3: limited foods, NOT easy to recognize (factor reliability = 0.91).
As shown in Table 2, the overall proportion of variance explained was 56%; 35% corresponding to factor 1, 14% to factor 2 and 7% to factor 3. The fit indices are shown in Table 3.

4. Discussion

Expert review and psychometric analyses support the use of a translated and adapted version of the questionnaire to evaluate knowledge of the low Phe diet in PKU. The questionnaire was designed to identify misinformation and gaps in knowledge regarding allowed and prohibited foods for individuals required to follow a diet for PKU. The results from the questionnaire provide a tool for dieticians and other healthcare providers advising parents and patients with PKU.
In addition, the questionnaire can be used in conjunction with new technologies, such as mobile apps or PKU-related games that can extend such training and permit access to materials and resources beyond specific advice. The questionnaire is quick to administer, easy to understand, and reliable. This is the first questionnaire designed for this purpose to be administered by healthcare professionals.
Participants in this study were not recruited based on the phenotype of the child with PKU. Thus, some individuals with milder phenotypes may be correct in identifying some foods with relatively high Phe content as allowed. However, the questionnaire includes an item regarding type of PKU so that individual results can be interpreted with this information in mind. The adaptation of the questionnaire to American English revealed some differences related to expressions, the use of some foods and words to define them. Thus, when used with individuals from other countries or for whom English is not a first language, some items may need to be explained or interpreted. In general, though, study participants accepted the questionnaire and found it easy to understand and complete.
The questionnaire is now available in translated and adapted versions in the US and Spain and may soon be available in Denmark and Estonia. Future research including cross-cultural studies correlating questionnaire results and indices of metabolic control will add to the understanding of factors related to dietary adherence in PKU.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/nu13082719/s1, PKU Questionnaire to Evaluate Knowledge of the Low Phe Diet.

Author Contributions

Design of the study and methodology, R.R.-Á. and S.E.W.; adaptation of the questionnaire to the US population, S.E.W., R.R.-Á. and M.K.; data collection, R.R.-Á. and M.K.; statistical data analysis, M.M.R.-R.; writing—original draft preparation, M.M.R.-R.; writing—review and editing, S.E.W., K.A., R.R.-Á., M.M.R.-R., M.A.B.-D., R.F. and M.K.; supervision, S.E.W., K.A. and R.R.-Á. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by a grant from the Vice-Rectorate for Scientific Policy and Research of the Granada University, through a Contract Program between the Faculty of Education and Humanities of Melilla and the University of Granada (project number 3/12-14). The cost for the open access publishing was covered by the company Danone Specialized Nutrition.

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki and approved by the Institutional Review Board of the Vice-Rectorate for Scientific Policy and Research at Granada University, Melilla Campus, on 15 June 2011, renewed on 1 June 2012 and 27 September 2016. The study in the USA was revised by the National PKU Alliance.

Informed Consent Statement

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

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Acknowledgments

The authors would like to acknowledge and thank all the patients and families participating in this study for their invaluable contributions. We want to thank the General Council of Psychology of Spain for the support and the development and computer adaptation of the questionnaire. We would like to acknowledge and thank the Vice-Rectorate for Scientific Policy and Research at Granada University, Melilla Campus, and the National PKU Alliance for approving this research. We would like to thank the California Coalition for PKU and Allied Disorders (CCPKUAD), especially Diane Pytel, for collaborating in the development of this questionnaire. The authors would like to thank Danone Specialized Nutrition for supporting the open access publishing.

Conflicts of Interest

The authors declare no conflict of interest. The authors have no conflict of interest with the company that covered the cost for the open access publishing.

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Table
Table 1. Demographic characteristics of the participants.
Table 1. Demographic characteristics of the participants.
OnlinePaperTotal
Total participants n (%)153 (86.45)24 (13.55)177 (100)
Gender n (%)
Males16 (10.46)6 (25.0)22 (12.43)
Females137 (89.54)18 (75.0)155 (87.57)
Level of education n (%) Primary school
5 (3.26)0 (0)5 (2.82)
Secondary school18 (11.77)1 (4.17)19 (10.74)
ParentsCollege/University130 (84.97)23 (95.83)153 (86.44)
Relationship to the PKU
Child n (%)
No answer0 (0)1 (4.16)1 (0.56)
Father13 (8.5)3 (12.5)16 (9.03)
Mother131 (85.62)17 (70.84)148 (83.62)
Other9 (5.88)3 (12.5)12 (6.79)
Sex n (%)
Boy80 (52.28)7 (29.17)80 (52.28)
Girl73 (47.72)17 (70.83)73 (47.71)
Level of education n (%) Daycare or preschool
75 (49.01)2 (8.33)77 (43.5)
Child withKindergarten13 (8.5)0 (0)13 (7.35)
PKUPrimary school46 (30.06)9 (37.50)55 (31,07)
Secondary school19 (12.43)13 (54.17)32 (18.08)
Type of PKU n (%)
Mild13 (8.5)1 (4.16)14 (7.9)
Moderate20 (13.07)1 (4.16)21 (11.87)
Classical107 (69.93)19 (79.2)126 (71.19)
Do not know/do not wish to answer13 (8.5)3 (12.48)16 (9.04)
Table
Table 2. Factorial structure of questionnaire.
Table 2. Factorial structure of questionnaire.
Factor 1: Allowed FoodsFactor 2: Forbidden Foods,
Easy to Recognize		Factor 3: Limited Foods,
NOT Easy to Recognize
PepperDiet CokePumpkin
PineappleNachosRice
Canned FruitFlourFrench Fries
KetchupBeansRoasted Potatoes
OnionSunflower seedsCoconut
LettuceGranola type cerealGreen peas
SyrupHot chocolate mixBroccoli
PicklesHazelnutsAvocado
OrangeBeef BouillonArtichoke
WatermelonEgg WhiteDark Chocolate
Fresh orange juice
Melon Kiwi
Olives
Plum		 Banana
Table
Table 3. Goodness of fit statistics.
Table 3. Goodness of fit statistics.
χ2NNFICFIGFIAGFI
Model912.49 (df = 493)0.860.890.990.99
Independence model4324.51 (df = 595)
Index without diagonal values 0.990.98
Note: χ2 = Chi-Square; df = degrees of freedom; NNFI = non-normalized fit index (Tucker and Lewis, 1973) [36]; CFI = comparative Fit Index; GFI = goodness of fit index; AGFI = adjusted goodness of fit index.
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Ramos-Álvarez, R.; Kapp, M.; Rodríguez-Ruiz, M.M.; Fausor, R.; Bueno-Delgado, M.A.; Ahring, K.; Waisbren, S.E. Adaptation and Validation of a Questionnaire to Evaluate Knowledge of the Low Phe Diet in PKU. Nutrients 2021, 13, 2719. https://doi.org/10.3390/nu13082719

AMA Style

Ramos-Álvarez R, Kapp M, Rodríguez-Ruiz MM, Fausor R, Bueno-Delgado MA, Ahring K, Waisbren SE. Adaptation and Validation of a Questionnaire to Evaluate Knowledge of the Low Phe Diet in PKU. Nutrients. 2021; 13(8):2719. https://doi.org/10.3390/nu13082719

Chicago/Turabian Style

Ramos-Álvarez, Rodolfo, Maili Kapp, María Mercedes Rodríguez-Ruiz, Rocío Fausor, María Amor Bueno-Delgado, Kirsten Ahring, and Susan E. Waisbren. 2021. "Adaptation and Validation of a Questionnaire to Evaluate Knowledge of the Low Phe Diet in PKU" Nutrients 13, no. 8: 2719. https://doi.org/10.3390/nu13082719

APA Style

Ramos-Álvarez, R., Kapp, M., Rodríguez-Ruiz, M. M., Fausor, R., Bueno-Delgado, M. A., Ahring, K., & Waisbren, S. E. (2021). Adaptation and Validation of a Questionnaire to Evaluate Knowledge of the Low Phe Diet in PKU. Nutrients, 13(8), 2719. https://doi.org/10.3390/nu13082719

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