Keywords
high-protein diet, hs-CRP, obese,weight cycling
This article is included in the All trials matter collection.
high-protein diet, hs-CRP, obese,weight cycling
The global prevalence of obesity according to the World Health Organization (WHO) in 1980 was 5% in the male population and 8% in the female population. In 2014, this increased to 38% in men aged over 18 years and 40% in women. The WHO stated that in the Southeast Asian regions, the prevalence of overweight population varies from 7.6% in male adults in Bangladesh to 53% female adults in Maldives1,2. In Indonesia, a report by RISKESDAS showed that the prevalence of central obesity increased from 18.8% in 2007 to 26.6% in 2013, and the prevalence for males aged >18 years old in the country was 19.7% and females >18 years old was 32.9%. Jakarta province has an obesity prevalence higher than the national rate, 30% for men and 40% for women3.
Obesity is associated with various health problems, mainly hypertension, cardiovascular diseases, dyslipidemia, diabetes, sleep apnea, and osteoarthritis. Obese people are more likely to be disabled in their later years, and many obese-related illnesses cause people in productive years to lose their productivity4. Attempts to lose weight by managing dietary intake and increasing physical activity are frequently conducted by many people, but the difficulty in maintaining body weight causes a fluctuation in body weight, called weight cycling5,6. A study by Votruba et al. (2002) reported that 16 (57%) of 28 women regained 19% of the body weight they lost after 1 year of follow-up7.
Obesity is accompanied by low-grade inflammation, which contributes to the development of cardiac complications4. The mild increase in hs-CRP levels, as an indicator of low-grade inflammation, is an indepent predictive factor of future cardiovascular diseases8. C-reactive protein (CRP) is an abnormal protein that appears in the blood during inflammation. Highly specific (hs-CRP) test can detect low CRP levels (0,2 mg/L) compared to CRP (N≤5 mg/L)4,9. A previous study by Azadbakht et al. showed that energy-restricted HP and SP diet brought about similar hs-CRP reduction in overweight and obese people8. Further studies are needed to asesss whether in obese individuals with weight cycling history, protein composition could affect inflammation markers. Therefore, the dietary composition that will give the best results for body composition as well as inflammation marker improvement for such population should be investigated. The aim of this study is to evaluate the effects of a low calorie high protein diet compared to a standard protein diet on the level of hs-CRP.
This is a part of an open-randomized parallel trial assessing the effect of a weight loss program with low calorie high protein diet conducted through dietary consultation on body composition, oxidative stress, inflammation marker and metabolic syndrome in obese individuals with weight cycling. The main interest of this article is the change of hsCRP levels among the HP and SP group before and after completing this program. There are two intervention groups with the allocation ratio 1:1, namely high protein (HP) group and standard protein (SP) group. There were no changes made to the methods after the study had been started (original trial protocol can be found in our sister article10).
Approval from the Health Research Ethical Committee of the Faculty of Medicine Universitas Indonesia – Cipto Mangunkusumo Hospital has been obtained by the letter number 237/UN2.F1/ETIK/2017. Written informed consent for participation in the trial and publication of patient information was obtained from each patient. A completed CONSORT checklist can be found in Supplementary File 1.
Trial registration number: NCT03374150
Registry name: Clinicaltrials.gov
Date of trial registration: 12/03/2017
Trial link: https://clinicaltrials.gov/show/NCT03374150
This study was conducted at the province’s Civil Workers’ Health Service Centre of the Special Capital Region of Jakarta (Pusat Pelayanan Kesehatan Pegawai Provinsi DKI Jakarta). Initial screening criteria for subject inclusion was men and women age > 20 years old with body mass index ranged 25 – 35 kg/m2. In this study, weight cycling was defined by history of weight loss ≥2 kg and regaining weight into or exceeding its initial body weight at least twice in last five years. Weight cycling history was obtained from a questionnaire regarding history of body weight changes (see supplementary materials of our sister article10). Subjects were excluded if they had diabetes mellitus, history of gastrointestinal tract resection, hormonal disorders, using hormonal contraception, menopause, and having kidney function disruption, which was identified from serum urea and creatinine levels. The recruitment and intervention were conducted in two periods, namely May – July and July – September of 2017.
All subjects who meet the inclusion criteria were measured for anthropometric data and were instructed to cease their previous diet program and requested to continue performing their daily physical activity at a regular level. History of previous daily calorie intake was gained from food recall interview 24 hours by asking type, cooking method, and estimation of amount of food consumed using household size, based on food photo books issued by Tim Survey Konsumsi Makanan Individu, Ministry of Health of Indonesia.
Dietary consultation for weight loss program was given for each subject in which all of them were suggested to reduce their daily caloric intake by 1000 kcal from their regular amount with lower limit of 1000 kcal/day. Subjects of HP group were assigned to low calorie-high protein diet with a composition of 22–30% protein, 50–55% carbohydrate, 20–25% fat while SP group were low calorie-balanced composition diet with 12–20% protein, 55–60% carbohydrate, and 20–30% fat. In order to ensure the compliance, follow-up to each subject were conducted by weekly person-to-person encounter with nutritionist and daily text reminder Subjects were equipped with diet formula, and logbook. Dietary program was applied for 8 weeks and subjects were instructed to fill logbook everyday to record their food intake. The measurement for hs-CRP level was done pre-intervention and re-measured after each subject has completed the 8 weeks of diet intervention.
A total of 28 participants would be needed in order that the difference between groups could be detected with a two-tailed α of 0.05 and a (1-β) of 0.80. Subject allocation into the intervention arms was determined through block randomization method with a block size of two. The group allocation sequence was constructed by the investigator (JJ) by random number generation method in which a computer-generated random number was taken, even number represent an arrangement of HP-SP and vice versa. The allocation sequence for all the participants that will be used throughout the study was generated by the investigator before the study commenced. Envelopes each representing a particular group were arranged according to the allocation sequence and then were orderly numbered. It was given consecutively to each subject who come hence the allocation sequence was blinded from the subject. The investigator assigned the subjects to the treatment group according to the envelope he/she received.
The primary data of this study is serum hs-CRP level before and after the diet intervention, which was measured using Immunochemmiluminescent device (Immulite 1000 Immunoassay system, Siemens Healthineers, Erlangen, Germany). The secondary outcome was dietary profile comprising mean daily caloric intake and mean daily proportion of macronutrients during the 56-days of diet program. Dietary data was measured with 24 hours food recall, while subject’s physical activity was calculated using Global Physical Activity Questionnaire from the WHO. Body weight and BMI measurement were conducted using 8-electrode method of Bio-Electrical Impedance Analysis (BIA; SC-330 Tanita Corp. Tokyo, Japan). No change to the outcome measures was done after the study commenced.
The characteristics of subjects were analyzed statistically using independent sample t-test (age and previous calorie intake), Fisher’s exact test (gender and weight cycling history), and Mann-Whitney test (weight and Body Mass Index (BMI)). All data except for body weight in HP group given as mean wih 95% confidence interval. Thirty-six subjecs were included for analysis. Change in body weight and BMI analyzed statistically using independent sample t-test, while intragroup pre- and post- mean difference of body weight and BMI analyzed by Wilcoxon test. The value of measured hs-CRP analyzed statistically by Mann-Whitney test. Statistical analysis was performed using SPSS for Windows version 20.
The number of participants who were screened, randomised and allocated into treatment, completed the treatment and analysed are provided in Figure 1. There were 54 participants completed the 56-days of diet program but only 15 subjects from SP group and 17 subjects from HP group who completed the treatment and had their hsCRP been measured were analyzed for the primary outcome to the group they were initally assigned. During the course of treatment, no major harms were reported by the participants.
Characteristics of subjects are presented in Table 1. There is no statistically significant difference found in the subjects’ characteristics. Meanwhile, dietary profile of the subjects among both groups during the 56-days of dietary programme were presented in the Table 2. Subjects’ body weight and BMI before and after the programme as well as the difference are provided in Table 3. The body weight, BMI, as well as the change in the body weight and BMI before and after the diet programme were higher in the SP group than the HP group, although those were not statistically significant. SP and HP groups both showed significant intragroup mean difference in body weight and BMI reduction pre- and post intervention. SP group experienced slightly greater reduction in body weight and BMI compared to HP protein (body weight 0.216, BMI p=0.136). The hs-CRP level before and after completing the intervention are provided in the Table 4. The hs-CRP level before (P=0.094) and after (P=0.063) the diet programme were higher in the SP group than in the HP group. After completing the 56-day diet programme, SP group experienced reduction of hs-CRP by -0.446 ± 4.239 while HP underwent overall increase by 0.135 ± 2.389 (p=0.094).
Only subjects who completed the study were included.
Variable | Standard protein group (n=15) | High protein group (n=17) | P value* |
---|---|---|---|
Age (years) | 33.4 ± 8.6 | 35.12 ± 8.8 | 0.598t |
Gender (n, %) | |||
Male | 1 (6.7) | 3 (17.6) | 0.603f |
Female | 14 (93.3) | 14 (82.4) | |
Body composition (mean±SD) | |||
Weight (kg) | 76.9 ± 8.55 | 74.0 ± 12.64 | 0.496m |
Body mass index (kg/m2) | 29.94 ± 2.79 | 29.16 ± 3.52 | 0.385m |
Frequency of weight cycling history (n, %) | |||
2–3 times | 11 (73.3) | 14 (81.7) | 0.907p |
4–5 times | 4 (26.7) | 3 (17.7) | |
Usual daily caloric intake (mean±SD) | 1759.3 ± 345.6 | 1802.3 ± 452.7 | 0.767t |
Physical activity level | |||
Very low | 3 (20) | 0 (0) | 0.152 |
Low | 8 (53.3) | 11 (64.7) | |
Moderate | 4 (26.7) | 6 (35.3) |
Variable | Standard protein (n=15) | High protein (n=17) | P-value* |
---|---|---|---|
Mean caloric intake (kcal; mean±SD) | 964.7 ± 83.33 | 1032.8 ± 177.27 | 0.184t |
Mean percentage of caloric intake from carbohydrate (%;mean±SD) | 50.73 ± 4.23 | 40.6 ± 5.22 | <0.001t |
Mean percentage of caloric intake from protein (%;mean±SD) | 20.91 ± 2.57 | 27.74 ± 3.31 | <0.001m |
Mean percentage of caloric intake from fat (%;mean±SD) | 21.05 ± 3.49 | 24.66 ± 3.73 | 0.009t |
Number of days with diet program compliance* (mean±SD) | 20 ± 9 | 26 ± 12 | 0.741t |
Group (mean±SD) | Standard group (n=15) | High protein (n=17) | P* |
---|---|---|---|
Body weight before intervention | 76.9 ± 8.55 | 74.0 ± 12.64 | 0.313m |
Body weight after intervention | 71.8 ± 9.98 | 70.07 ± 11.97 | 0.406m |
Intragroup pre- and post- mean difference significance | P<0.001 | P<0.001 | |
Body mass index before intervention | 29.9 ± 2.79 | 29.16 ± 3.52 | 0.496t |
Body mass index after intervention | 27.96 ± 3.42 | 27.68 ± 3.39 | 0.815t |
Intragroup pre- and post- mean difference significance | P<0.001 | P<0.001 | |
Change in body weight | -5.1 ± 2.57 | -4.0 ± 2.33 | 0.216t |
Change in BMI | -1.97 ± 1.01 | -1.47 ± 0.83 | 0.136t |
hs-CRP | Group of intervention | P-value | |
---|---|---|---|
SP group (n=15) | HP group (n=17) | ||
hs-CRP before intervention | 6.08 ± 3.99 | 3.84 ± 3.75 | 0.094m |
hs-CRP after intervention | 5.63 ± 5.65 | 3.97 ± 4.51 | 0.063m |
Intragroup pre- and post- mean difference significance | 0.105w | 0.586w | |
Change in the hs-CRP | -0.446 ± 4.239 | 0.135 ± 2.389 | 0.094m |
Mean difference of change in hsCRP (95%CI) | 0.582 ((-1.864) - 3.028) |
The baseline and post-treatment hs-CRP level of HP group was lower than that of the SP group, although both were insignificant. The change of hs-CRP level of both group were also statistically insignificant. While the mean hs-CRP level of HP group increased, in the SP group it decreased. The insignificant reduction in hs-CRP despite weight loss and the decrease of BMI may because all the subjects were still in the overweight or obese state. Adipokines released by adypocites or macrophages induced low-grade chronic inflammation in overweight and obese people11; hence the hs-CRP level as the indicator of such condition is maintained.
The result of this study is similar to a study by Due et al., in which SP diet in overweight subjects showed a better reduction of hs-CRP than HP diet12. The result is also in line with a study by Azadbakht et al. on the effects of HP diet to weight, cardiovascular risk and hs-CRP. Between the HP-low calorie diet (protein, carbohydrate, and fat: 25%, 45%, and 30% respectively) and SP-low calorie diet (protein, carbohydrate and fat : 15%, 55%, and 30%), hs-CRP in the standard group decreased greater by which it reduced −0.08 ± 0.11%, while in the HP group it only reduced by −0.04 ± 0.09% (p=0.06)13. Another study by Kitabchi et al., which compared various metabolic marker in the HP diet and high carbohydrate diet for 6 months showed a greater decrease of inflammation marker (CRP) in the group receiving high carbohydrate diet than in the HP group (-2,1 vs. -0.8 mg/L, p=0.0003)14.
Despite the benefit of higher protein diet in increasing satiety, the present study found that SP composition provided larger reduction in body weight and hs-CRP level compared to HP group. The amino acids obtained from protein intake were absorbed then are passed into the liver. The rate of synthesis and degradation of amino acids there is influenced by many factors including immediate food intake and nutritional status14. Inflammation and physical inactivity in the weight cycling condition which were characterized by accelerated wasting of lean body mass lead to the accelerated depletion of amino acids obtained from the dietary protein intake to counter the amino acids loss during the degradation of protein from body mass15.
A major limitation of this study is the absence of detailed assessment of the condition of the participants during the course of the intervention, such as the presence of acute illness, the use of drugs that affect the body inflammatory state and so on, which potentially affect the level of hs-CRP. Besides, the dietary consultation failed to maintain the compliance of the participants to the dietary plan to the desired extent. The average number of days in which subjects comply towards the assigned program is only 20 days in the SP group and 26 in the HP group which may further limit the validity of this study. The majority of participants of this study were office workers which may limit the generalisability of this study.
Although both standard and high protein low-calorie diet for 56 days reduced body weight and BMI significantly in obese people with weight cycling, SP diet of 12–20% of overall daily caloric intake decreased hs-CRP levels, as an inflammation marker, greater than HP diet. However, the mean difference of change in hs-CRP level between the two groups were not statistically significant. This is probably due to the subjects from both groups were still in the obese/overweight state hence the change in the level of inflammation marker were less prominent. A trial with larger participants and/or longer follow-up period are needed to confirm whether protein proportion of dietary programme affects the change in serum hs-CRP level.
Dataset 1: Harvard Dataverse. Replication Data for Comparison of low calorie-standard protein or high protein diet on body composition, malondialdehyde and glutathione, and hs-CRP level, http://dx.doi.org/10.7910/DVN/7H55FP16
Data are available under the terms of the Creative Commons Zero "No rights reserved" data waiver (CC0 1.0 Public domain dedication).
Publikasi Internasional Terindeks Untuk Tugas Akhir Mahasiswa (PITTA) grant 2017, Directorate of Research and Community Services (DRPM) Universitas Indonesia.
The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
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Is the work clearly and accurately presented and does it cite the current literature?
Partly
Is the study design appropriate and is the work technically sound?
No
Are sufficient details of methods and analysis provided to allow replication by others?
No
If applicable, is the statistical analysis and its interpretation appropriate?
No
Are all the source data underlying the results available to ensure full reproducibility?
No
Are the conclusions drawn adequately supported by the results?
No
Competing Interests: No competing interests were disclosed.
Reviewer Expertise: Renal nutrition
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