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. 2024 Jun;48(6):884-890.
doi: 10.1038/s41366-024-01492-9. Epub 2024 Feb 28.

Cumulative effect of obesity phenotypes on body weight and body mass index

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Cumulative effect of obesity phenotypes on body weight and body mass index

Wissam Ghusn et al. Int J Obes (Lond). 2024 Jun.

Abstract

Background: Obesity originates from an imbalance between energy intake and expenditure. Changes in energy intake components (satiation, postprandial satiety, emotional eating) and energy expenditure have been linked to obesity and are referred to as obesity phenotypes. We aim to study if these obesity phenotypes have a cumulative effect on body weight and body mass index (BMI).

Subject/methods: This is a cross-sectional study of adult patients with obesity (BMI > 30 kg/m2) who completed the validated tests to measure the obesity phenotypes. A total of 464 were included in this study.

Interventions/methods: We defined higher calories to fullness during an ad libitum meal as abnormal satiation, accelerated time to half gastric emptying with scintigraphy as abnormal postprandial satiety, higher anxiety score on the Hospital Anxiety and Depression Scale as hedonic eating behavior, and decreased percentage of measured resting energy expenditure as abnormal energy expenditure. The primary analysis was done on the number of phenotypes ( ≤ 1 and ≥ 2) with body weight and BMI using an independent t-test.

Results: Our cohort included 464 patients (mean [SD] age 42.0 [10.9] years, 79% females, weight 111.2 [22.9] kg, BMI 38.9 [7.0] kg/m2). There were 294 patients who had ≤ 1 phenotype, and 170 patients with ≥ 2 phenotypes with no baseline demographical differences (i.e., age and sex). Having ≥ 2 phenotypes was associated with higher body weight (115 [25] kg vs. 109 [21] kg; p = 0.004), BMI (40 [8] kg/m2 vs. 38 [7] kg/m2; p = 0.02) and waist (118 [15] cm vs. 115 [13] cm; p = 0.04) and hip (129 [14] cm vs. 125 [13] cm; p = 0.01) circumferences compared to ≤ 1 phenotype.

Conclusion: Obesity phenotypes are associated with an additive effect on the body weight and BMI. Patients who have multiple obesity phenotypes may require a more aggressive approach to enhance weight loss.

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Conflict of interest statement

COMPETING INTERESTS

Dr. Acosta is a stockholder in Gila Therapeutics, Phenomix Sciences; he served as a consultant for Rhythm Pharmaceuticals, Nestle, Structure Therapeutics and Amgen Pharmaceuticals. There are no other disclosures. All other authors declare no competing financial interests.

Figures

Fig. 1
Fig. 1. Clinical tests to classify obesity phenotypes.
Distribution of patients based on obesity phenotypes.
Fig. 2
Fig. 2. Association between number of obesity phenotypes and clinical parameters.
Body weight (A), BMI (B), waist (C), and hip (D) circumferences in patients with ≤ 1 obesity phenotype compared to ≥ 2 phenotypes. Data are presented in mean (SEM). *p < 0.05; **p < 0.01; ***p < 0.001.
Fig. 3
Fig. 3. Association between number of obesity phenotypes and clinical parameters.
Body weight (A), BMI (B), waist (C), and hip (D) circumferences in patients with 0, 1, 2, and 3+ obesity phenotypes. Data are presented in mean (SEM). *p < 0.05; **p < 0.01; ***p < 0.001.

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