1. Introduction
Phenylketonuria (PKU) is a genetic condition in which there is an inability to metabolise the amino acid phenylalanine into tyrosine. The treatment strategy for this condition is a lifelong phenylalanine-restricted diet to prevent adverse neurocognitive and psychological outcomes. This maintains blood phenylalanine levels within a narrow target therapeutic range but still delivers enough phenylalanine to support physiological protein synthesis, growth, and development. Patients with classical phenotypes usually have a natural protein tolerance that limits amounts to only 20% or less of what is expected in a regular diet [
1]. High-protein foods such as meat, fish, eggs, cheese, seeds, and nuts are avoided with controlled and measured intakes of cereals, potato, breakfast cereals, and some vegetables allocated in a 1 g protein exchange system (1 exchange is equivalent to ~50 mg phenylalanine) [
1]. The amount of natural protein tolerated is individual and influenced by the patient’s phenotype, use of adjunct therapy (such as sapropterin), growth rate, and dosage of protein substitute intake.
Since the 1960s, the UK has adopted a straightforward approach to dietary management, allocating foods such as fruit and vegetables containing phenylalanine up to 75 mg/100 g weight without measurement. Although there is a long history of including manufactured foods in a protein-restricted diet, the range of prepackaged foods available has exponentially increased, and food choice is now almost indefinable. Every major British supermarket stocks 30,000 to 40,000 consumable items, including a diverse range of prepackaged foods. The breadth of food additives is continually expanding, and many prepackaged foods contain a multitude of ingredients with some contributing extra protein or phenylalanine, such as artificial sweeteners, spirulina extract as a colour additive; cereal; gelatine thickeners and taste enhancers, e.g., yeast extracts. In particular, aspartame, an artificial sweetener, is a peptide rich in phenylalanine. In the EU and UK, prepackaged foods should list the protein content as one of six mandatory nutrients and state the amount of protein per 100 g or per 100 millilitres [
2]. However, it is not mandatory to issue food label warnings if the food product recipe changes and alters the nutritional content. Navigating food labels and understanding the suitability of individual manufactured foods has intensified the complexity of dietary management.
In 2020, the British Inherited Metabolic Disease Dietitians Group (BIMDG-DG) published consensus statements about the suitability of foods in a phenylalanine-restricted diet for PKU to help standardise interpretation, particularly of prepackaged foods [
3]. Statements divided food and drink into categories based on defined protein content. It included foods allowed without restriction, which contain protein ≤0.5 g/100 g, and foods that should be calculated/weighed as an exchange food if they contain protein exchange ingredients (categorised into foods with a protein content of: >0.1 g/100 g (milk/plant milks only), >0.5 g/100 g (bread/pasta/cereal/flours), >1 g/100 g (cook-in/tabletop sauces/dressings), and >1.5 g/100 g (soya sauces) [
3]. The practical statements were endorsed and translated into practical dietary advice for patients and caregivers by the National Society for PKU (NSPKU).
In order for patients/caregivers to fully adhere to dietary management, they are expected to acquire expert knowledge about the protein content of foods. It is the role of dietitians specialising in inherited metabolic disorders to teach parents and patients about the application of the complex set of BIMDG dietary rules. This enables patients/caregivers to understand and interpret food label ingredient lists and explain how to calculate 1 g protein exchanges directly from protein labelling. Patients and caregivers are given a range of dietary resources, including ‘pocket’ protein exchange calculators, dietary information books, detailed food lists, and a collection of suitable manufactured food picture books.
In practice, reading and interpreting food labels adds an additional task to a dietary regimen already associated with a heavy time burden [
4]. The ability of adults with PKU/caregivers to calculate protein exchanges and any difficulties they encounter in interpreting food labels and calculating protein exchanges have not been studied systematically. This project aimed to explore the perception and opinion of patients with PKU and their caregivers about their experiences when calculating protein exchanges from the food labelling of prepackaged foods.
2. Materials and Methods
2.1. Methodology
This was a cross-sectional study using an online survey collecting qualitative and quantitative data from caregivers of children with PKU and adult patients. Respondents were excluded if they did not reside in the UK.
The questionnaire was built in an Online Surveys platform (
https://www.onlinesurveys.ac.uk, accessed on 17 July 2020). This was shared on the UK National Society for Phenylketonuria (NSPKU) website, with additional promotion on the NSPKU Twitter, Instagram, and Facebook sites. The questionnaire was open from the 18 July 2020 until the 1 February 2021.
2.2. Questionnaire
The non-validated questionnaire contained 24 questions. There were fourteen multiple-choice, four multiple-responses, and six open-ended questions. Five questions consisted of more than one part (2–7 parts). Four other questions invited additional comments. There were 4 questions about alcohol labelling that were targeted at adults aged ≥18 years; these data will be included in a separate publication.
The questionnaire was developed by dietitians with expert practical and scientific knowledge of PKU (AP, SE, CA, AD, AM), a colleague from the NSPKU (SF), and a student dietitian from Birmingham City University (IH). It was reviewed by colleagues and lay people to ensure its readability and then amended according to feedback.
2.3. Data Collected
The questionnaire was divided into 3 sections.
Section 1 collected information on patient age, sex, type of supermarket they commonly shopped at, and ease of calculating protein exchanges from food analysis labels for known problems previously identified [
5].
These included 4 groups of manufactured foods:
- (1)
Stock cubes, gravy granules, dried sauce powders, tabletop sauces, cooking sauces, curry paste;
- (2)
Tinned tomatoes, tomato puree, dried soups, tinned or soup pots;
- (3)
Dried custard, ready-made custard, instant dessert powders, milkshake powders, milkshake liquids, drinking chocolate powder, ice cream, ice lollies;
- (4)
Dried rice, cooked rice, microwave rice, dried noodles, pot noodles.
Section 2 contained information about interpreting the protein content of alcohol that was only collected from adults.
Section 3 contained information collected about the problems with food labelling, examples of issues experienced in the previous 6 months, the respondents’ approach to dealing with food labelling issues, emotions when identifying misleading labelling, and changes that should be made to food labelling legislation. All data collected were based on the patient’s/caregiver’s knowledge of their own experiences when interpreting the suitability of foods and calculating protein exchanges from food labelling.
2.4. Statistics
Questions were analysed with descriptive statistics only.
Qualitative data analyses of open-ended responses were carried out in NVIVO v 12 PRO (QSR International Pty Ltd., Australia, New Zealand and Oceania Level 5, Suite 5.11 737 Burwood Road Hawthorn East, Vic 3123). The whole survey dataset was imported into NVIVO so that coding of open-ended responses could be broken down by survey questions. All open-ended question responses were analysed thematically.
2.5. Ethics
Ethical approval was obtained from the Birmingham City University Ethics Committee prior to commencement of the study (Hall/7499/R(B)/2020/Jul/HELS FAEC–MSc Healthcare Project: What are the current issues with protein labelling for PKU patients?). At the beginning of the online questionnaire, respondents gave consent, and it was emphasised that questionnaire completion was voluntary. Potential respondents were advised that data from the survey would be published in an anonymised form. Names or hospitals mentioned in verbatim abstracts were removed from results presented in this manuscript.
3. Results
3.1. Demographics
Two hundred and forty-six respondents from the UK answered the questionnaire. Twenty-three per cent (n = 57/246) were adults with PKU (aged >18 years), 11% (n = 28/246) were parents/caregivers of adults with PKU, 62% (n = 152/246) were parents of children with PKU, and 4% (n = 9/246) were children/teenagers with PKU. Forty-eight per cent (n = 117/246) of the respondents or respondent’s children with PKU were male, 50% (n = 124/246) female, and 2% (n = 4/246) non-binary, and one respondent (0.4%) preferred not to answer. The four main regular supermarkets used by respondents were: Tesco (62%, n = 153/246), Asda (54%, n = 132/246), Aldi (39%, n = 97/246), and Sainsbury’s (39%, n = 95/246).
3.2. Rating of Food Labelling in General
This received a mixed response from respondents, with 2% (n = 5/246) describing it as very good, 41% (n = 101/246) as fairly good, 30% (n = 74/246) as neither good nor bad; 19% (n = 47/246) as fairly bad, 7% (n = 17/246) as poor, and 1% (n = 2/246) did not know.
3.3. Ease of Calculating Protein Exchanges from Food Labels
There was difficulty in calculating protein exchanges from food labels for food and drinks for at least one-third of the respondents (
Table 1). For some individually manufactured foods, increased problems were described, including dried powdered products such as sauces, soups, dessert powders, dried custard powders, drinking chocolates, pot noodles, and noodles. In an open comment question, 398 verbatim comments were received about food labelling. The mixed responses were thematically analysed into the following categories: (1) finding food labelling easy to understand, (2) difficulty with interpreting food content, (3) difficulty with understanding how to calculate protein exchanges, and (4) did not use protein labelling. Examples of responses are given in
Table 2.
Many respondents commented that protein labelling was unclear when the protein analysis was given after theoretical preparation, particularly when the manufacturers had assumed a product was prepared with cow’s milk or egg. Ice cream was complicated as protein analysis was commonly given by volume as mL rather than weight as g. Some commented that it was difficult when food products such as jelly or yoghurt had to be checked for both protein content and the presence of aspartame. It was also remarked that due to deficits with cognitive functioning, particularly mathematical and reading skills, some respondents were unable to calculate protein exchanges. Some respondents with sight difficulties were unable to read the small font of some food analysis labelling, and some did not calculate protein intake but preferred to use food picture books showing suitable manufactured foods provided to them by their hospitals and NSPKU, as they had confidence that these were likely to be correct. Others did not deviate from the foods they knew were safe and did not try new manufactured foods.
3.4. Main Issues with Protein Labelling
The respondents listed that the main issues with protein content on food labels were (
Table 3): not specifying if the protein content is for the cooked or uncooked weight; a manufactured food stating that it contains 0 g protein but the ingredients list contains a source of protein such as milk or gelatine; protein amount given only after a product has been prepared with regular milk; and non-clarity if the protein content was for prepared or unprepared food weight (in addition to cooked or uncooked weight).
3.5. Issues with Protein Food Labelling in the Previous 6 Months
Over 90% (
n = 222/246) had experienced problems with food labelling in the previous 6 months. In fact,
n = 97/246 (39%) identified having problems at least 10 times in the 6-month period, with
n = 68/246 (28%) describing weekly issues with food protein labelling. One hundred and sixteen respondents listed examples of problematic food labelling, and these were thematically analysed into nine categories: (1) inadequate aspartame warning (
n = 27); (2) dried products that are made up/served with milk (
n = 16); (3) no differentiation of dried, unprepared, or uncooked weight vs. cooked/prepared weight (
n = 16), (4) unclear protein labelling in general (
n = 13); (5) suspect/doubtful protein content (
n = 11); (6) foods purchased in multi-packs with unclear protein labelling (
n = 9); (7) recipe change of a food item without warning (
n = 9); (8) unclear protein content of imported foods (
n = 8); and (9) analysis of protein content by volume rather than weight (
n = 7). Examples of verbatim comments by the respondents are given in
Table 4.
If respondents were unsure about the interpretation of food labelling, the majority said they would not use the food products (57%, n = 140/246), 47% (n = 115/246) would ask their dietitian or other health professional for help, 30% (n = 73/246) would ask others on social media, and 14% (n = 35/246) would guess the protein content and use it. Eight per cent (n = 20/246) said they would either try looking at other sources of information on websites, ask their relatives, or try and calculate it themselves.
3.6. Respondent Emotions Associated with Food Labelling
Respondents reported that misleading or inadequate information on protein food labelling made them feel frustrated (67%, n = 165/246), anxious (33%, n = 82/246), angry (33%, n = 81/246), upset (28%, n = 70/246), unhappy (28%, n = 68/246), and excluded (27%, n = 67/246).
3.7. Suggested Changes to Food Labelling by Adults with PKU/Caregivers
Suggested changes to protein labelling are presented in
Table 5.
There were 33 other suggested changes, including that manufacturers should not assume that products are prepared with cow’s milk and give the protein analysis only after theoretical preparation; aspartame should always be in bold; all protein analysis should be made available on every supermarket website; and products should state accurate protein analysis and not use protein <0.5 g/100 g, which is unhelpful for low-protein diets. Some suggested that the protein content should always be in a uniform position on the food analysis list. It was also suggested that nutrient analysis should be in a larger font, and the protein content should be included on the front of the packet alongside the energy content.
4. Discussion
This paper highlights the considerable problems faced by both adult PKU patients and caregivers of children with PKU when trying to calculate exchanges from the protein analysis provided on food labels of prepackaged foods. Although there was a consensus that overall food labelling was satisfactory, the findings indicate that many patients/caregivers find protein calculations a complex process and identified several difficulties when interpreting protein labelling.
It was disconcerting that over 90% of respondents described specific issues with food labelling in the previous 6 months. Several respondents were frustrated that some potentially suitable instant dessert mixes and dried cereals had a protein content given on the food analysis after manufacturers had assumed they would be reconstituted/prepared with added cow’s milk or egg, rendering the products unsuitable for people with PKU; no data were provided about the protein content of the dry products as purchased. There were many examples of ice creams that gave protein content for volume (in millilitres) rather than weight, and prepackaged foods that only gave a protein content of <0.5 g/100 g. Some commented that it would make a ‘massive difference’ if food labelling was clearer as there would be more foods that could be consumed, that the ‘confusing protein labelling made it very hard when choosing suitable foods in the supermarket’, and ‘the problems of interpreting protein labelling will not help my son become independent.’ These issues were also identified by Kravela et al. 2020, who examined the accuracy of protein analysis from supermarket websites [
5].
It was worrying that some respondents identified that manufacturers changed the recipes of some of their products, affecting the protein content, without any ‘front of package’ warnings, possibly causing dietary error. This commonly occurred in foods such as breakfast cereals following the Public Health England voluntary sugar-reduction programme (2017), which requested that manufacturers lower the sugar content of foods by 20% [
6]. Some manufacturers replaced sugar with other ingredients containing protein. If people with PKU or their caregivers do not detect changes in protein labelling immediately, it may potentially lead to a long-term miscalculation of protein intake. It is well established that some patients with PKU struggle with maintaining satisfactory blood phenylalanine control [
7,
8,
9]. This is often attributed to poor dietary adherence, but inadequate standards of food protein labelling could contribute to this. Misinterpretation of protein food labelling may cause some of the day to day blood phenylalanine variation that is observed in PKU, although this remains an area not considered by researchers.
Respondents also described an unfortunate trend for average protein labelling on multi-packs of different individually wrapped foods (e.g., small boxes of breakfast cereals, mixed flavoured bags of popcorn and crisps, and sweets and chocolates) with each individual item in the multi-pack having a different protein content per 100 g. For many multi-packs, respondents described how the protein content was given as an average on the outer packs, with no protein content stated on individual packs. For one product, a different protein content was stated on the outer compared with the inner packaging, which suggested careless protein labelling practice by the manufacturer. There appears to be no mandatory law to inform manufacturers that this practice is misleading and unsafe for people with PKU as well as other patient groups following protein-restricted diets. It is extraordinary that the UK Food Standards Agency has allowed this practice to occur.
There was respondent mistrust around the accuracy of protein labelling, with examples given of discrepancies of protein analysis between websites and actual food product labelling. Some food products declared high-protein-containing ingredients in the first two or three items listed on their labels, yet the protein analysis was 0 g/100 g. One product contained less protein per 100 g than was given for an 80 g portion size. There were examples of decimal place typing errors that had clearly not been detected by the proofreaders of the manufacturer’s labels; this could have serious consequences for patients with PKU. There were descriptions of protein analyses being hidden/lost in packaging ‘folds,’ or the protein analysis being written in a linear format with other nutrients listed on the same line, making it difficult to distinguish protein from other nutrients. There were also important concerns about the protein labelling of imported foods. Food labels from the USA state protein content in portion sizes only. Imported foods from the USA only acknowledge the presence of protein on food labels if a prepackaged product contains more than 1 g of protein/portion; otherwise, they inaccurately state that the product contains 0 g of protein/portion. Some imported foods were reported to not include any English-language food analysis on the labels, although all labels need to comply with the UK food labelling laws, and this is mandatory.
Over one-third of respondents found drinks labelling a particular issue. Any alcoholic drink with a volume content above 1.2% does not legally require protein content to be declared, although appropriate allergen information should be given [
10]. Importantly, aspartame content is exempted from inclusion in the labelling of alcoholic drinks. [
11]. Several examples were given of inconsistent aspartame identification on the labels of fruit squashes or drinks bought from shop vendors. Detailed information about the perceptions of aspartame and food labelling of patients or caregivers of patients with PKU has been reported [
11].
Except for the mandatory guidelines that manufacturers should state the product protein analysis per 100 g or 100 mL, there are few legal requirements about protein labelling [
12]. The legislation allows manufacturers to use different methods to calculate the protein content of foods. It does not necessarily require laboratory analysis, and it may be possible for a food business operator themselves to perform a calculation from the known, or actual, average values of the ingredients used or to utilize established and accepted data [
13]. Food regulations consider that a protein amount of ≤0.5 g per 100 g or 100 mL to be negligible, and so neglects the needs of people with PKU. Manufacturers may give the protein content per portion and/or per consumption unit, but this is not mandatory [
2]. There is much that is lacking in protein legislation. Legislators must be aware that an inattentive approach to protein food labelling is a source of increased stress and burden for people with PKU and their caregivers. It limits their food choices, may induce unhealthy/repetitive food patterns, reduces variety in the diet, and may contribute to food neophobia [
14].
This study has some limitations. Recruitment of participants for the online survey was performed via the NSPKU website and promoted on PKU social media sites, so respondents were limited to individuals with access to the internet using appropriate technology. Hence, it is likely that respondents were people who accessed social media sites frequently, and their views may not fully represent those of the broader population of PKU patients or their caregivers. However, problems deciphering food labels may be just as frequent in non-social media users, and this could be further investigated. Although there was a large response from caregivers (
n = 180), there was a low response from adults with PKU (
n = 57). It is known that in England alone, there are around 1100 adults on diet therapy with PKU. It is unclear whether this was due to a low interest in this area; unchanging dietary habits; limited reading of food labels; or low usage of websites, or PKU sites in particular, by affected adults [
15]. The questionnaire was not validated prior to use, and the respondents’ levels of education were unknown. We did not examine the amount of teaching they had received about a phenylalanine-restricted diet, which may have affected their answers, and the data from adult patients were not compared with those of caregivers.