Abstract

Osteoporosis is a major public health problem with low bone mass affecting nearly half the women aged 50 years or older. Evidence from various studies has shown that higher body mass index (BMI) is a protective factor for bone mineral density (BMD). Most of the evidence, however, is from studies with Caucasian women and it is unclear to what extent ethnicity plays a role in modifying the effect of BMI on BMD.A cross sectional study was performed in which records of postmenopausal women who presented for screening for osteoporosis at 2 urban medical centres were reviewed. Using logistic regression, we examined the interaction of race and BMI after adjusting for age, family history of osteoporosis, maternal fracture, smoking, and sedentary lifestyle on BMD. Low BMD was defined as T-score at the lumbar spine < -1.Among 3,206 patients identified, the mean age of the study population was 58.3 ± 0.24 (Years ± SEM) and the BMI was 30.6 kg/m2. 2,417 (75.4%) were African Americans (AA), 441(13.6%) were Whites and 348 (10.9%) were Hispanics. The AA women had lower odds of having low BMD compared to Whites [Odds ratio (OR) = 0.079 (0.03–0.24) (95% CI), p < 0.01]. The odds ratio of low BMD was not statistically significant between White and Hispanic women. We examined the interaction between race and BMD. For White women; as the BMI increases by unity, the odds of low BMD decreases [OR = 0.9 (0.87–0.94), p < 0.01; for every unit increase in BMI]. AA women had slightly but significantly higher odds of low BMD compared to Whites [OR 1.015 (1.007–1.14), p <0.01 for every unit increase in BMI]. This effect was not observed when Hispanic women were compared to Whites.There is thus a race-dependent effect of BMI on BMD. With each unit increase in BMI, BMD increases for White women, while a slight but significant decrease in BMD occurs in African American women.

Highlights

  • Osteoporosis is a chronic bone disease characterized by low bone mass and microarchitectural disruption, leading to bone fragility and an increased susceptibility to fractures [1,2]

  • A total of 3,206 women were screened for postmenopausal osteoporosis with their clinic records subsequently reviewed (Table 1). 2,417 (75.4%) were African Americans (AA), 441(13.6%) were Whites, and 348 (10.9%) were Hispanics, reflecting the predominance of AA as the main ethnic group in the community examined

  • After adjusting for age, family history of osteoporosis, maternal fracture, smoking, and sedentary lifestyle, AA women had significantly lower odds of having low bone mineral density (BMD) compared to Whites [Odds ratio (OR) = 0.079 (0.03–0.24), p < 0.01]

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Summary

Introduction

Osteoporosis is a chronic bone disease characterized by low bone mass and microarchitectural disruption, leading to bone fragility and an increased susceptibility to fractures [1,2]. The National Osteoporosis Foundation reports that close to 22 million women aged 50 or older have low bone mass with projections thru year 2010 and 2020 reaching almost 26 million and over 30 million respectively [3,4,5]. The National Osteoporosis Risk Assessment (NORA) study, the largest study of postmenopausal osteoporosis conducted in the United States, with more than 200,000 women aged 50 or older, demonstrated low BMD in almost half of the study population [7]. These numbers, by any standard, portend substantial societal and economic burdens that underscore the importance of disease prevention

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