Effect of Protein Intake on Visceral Abdominal Fat and Metabolic Biomarkers in Older Men With Functional Limitations: Results From a Randomized Clinical Trial
Grace Huang, Karol Pencina, Zhuoying Li, Caroline M Apovian, Thomas G Travison, Thomas W Storer, Thiago Gagliano-Jucá, Shehzad Basaria, Shalender Bhasin, Grace Huang, Karol Pencina, Zhuoying Li, Caroline M Apovian, Thomas G Travison, Thomas W Storer, Thiago Gagliano-Jucá, Shehzad Basaria, Shalender Bhasin
Abstract
Background: It remains controversial whether high protein diets improve cardiometabolic profile. We investigated whether increasing protein intake to 1.3 g/kg/day in functionally limited older adults with usual protein intake ≤RDA (0.8 g/kg/day) improves visceral fat accumulation and serum cardiovascular risk markers more than the recommended daily allowance (RDA).
Methods: The Optimizing Protein Intake in Older Men Trial was a placebo-controlled, randomized trial in which 92 functionally limited men, ≥65 years, with usual protein intake ≤RDA were randomized for 6 months to: 0.8 g/kg/day protein plus placebo; 1.3 g/kg/day protein plus placebo; 0.8 g/kg/day protein plus testosterone enanthate 100 mg weekly; or 1.3 g/kg/day protein plus testosterone enanthate 100 mg weekly. In this substudy, metabolic and inflammatory serum markers were measured in 77 men, and visceral adipose tissue (VAT) was assessed using dual-energy x-ray absorptiometry in 56 men.
Results: Treatment groups were similar in their baseline characteristics. Randomization to 1.3 g/kg/day protein group was associated with greater reduction in VAT compared to 0.8 g/kg/day group (between-group difference: -17.3 cm2, 95% confidence interval [CI]: -29.7 to -4.8 cm2, p = .008), regardless of whether they received testosterone or placebo. Changes in fasting glucose, fasting insulin, HOMA-IR, leptin, adiponectin, IL-6, and hs-CRP did not differ between the 0.8 versus 1.3 g/kg/day protein groups regardless of testosterone use.
Conclusions: Protein intake >RDA decreased VAT in functionally limited older men but did not improve cardiovascular disease risk markers.
Clinical trials registration number: NCT01275365.
Keywords: Insulin resistance; Metabolic; Protein intake; Testosterone; Visceral fat.
© The Author(s) 2021. Published by Oxford University Press on behalf of The Gerontological Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
Figures
![Figure 1.](https://www.ncbi.nlm.nih.gov/pmc/articles/instance/8140050/bin/glab007f0001.jpg)
Source: PubMed