Literature DB >> 25825948

Sex Differences in the Effects of Weight Loss Diets on Bone Mineral Density and Body Composition: POUNDS LOST Trial.

Amir Tirosh1, Russell J de Souza1, Frank Sacks1, George A Bray1, Steven R Smith1, Meryl S LeBoff1.   

Abstract

CONTEXT: Weight loss is associated with reduction in bone mineral density (BMD).
OBJECTIVE: The objective was to address the role of changes in fat mass (FM) and lean mass (LM) in BMD decline in both sexes.
DESIGN: A 2-year randomized controlled trial, the Preventing Overweight Using Novel Dietary Strategies (POUNDS-LOST).
SETTING: The setting was the general community. PATIENTS OR OTHER PARTICIPANTS: Enrolled were 424 overweight and obese participants (mean age, 52 ± 9 y; 57% females). INTERVENTION: Intervention included weight loss diets differing in fat, protein, and carbohydrates. MAIN OUTCOME MEASURES: Main outcome measures were change in spine, total hip (TH), and femoral neck (FN) BMD and sex differences after dietary intervention.
RESULTS: At baseline, a stronger correlation between BMD and body composition measurements was observed in women, primarily with LM (r = 0.419, 0.507, and 0.523 for spine, FN, and TH, respectively; all P < .001). In men, only LM correlated with hip BMD (r = 0.298; P < .001). Mean weight loss at 2 years was -6.9%, without differences among diets. Two-year changes in BMD were 0.005 (P = .04), -0.014 (P < .001), and -0.014 g/cm(2) (P < .001), at the spine, TH, and FN, respectively. These changes directly correlated with changes in LM in women (r = 0.200, 0.324, and 0.260 for spine, FN, and TH, respectively), whereas FM loss correlated only with changes in TH BMD (0.274; P < .001). In men, changes in LM (-0.323; P < .001) and FM (-0.213; P = .027) negatively correlated with changes in spine BMD.
CONCLUSIONS: Weight loss diets result in sex-specific effects on BMD. Although men exhibited a paradoxical increase in spine BMD, women tended to decrease in BMD at all sites.

Entities:  

Mesh:

Year:  2015        PMID: 25825948      PMCID: PMC4454797          DOI: 10.1210/jc.2015-1050

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


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