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BMJ Open. 2012; 2(5): e001315.
Published online 2012 October 6. doi:  10.1136/bmjopen-2012-001315
PMCID: PMC3488758
A cross-sectional study of the association of age, race and ethnicity, and body mass index with sex steroid hormone marker profiles among men in the National Health and Nutrition Examination Survey (NHANES III)
Jamie Ritchey,1 Wilfried Karmaus,1 Tara Sabo-Attwood,1 Susan E Steck,1,2 and Hongmei Zhang1
1Epidemiology and Biostatistics, University of South Carolina, Columbia, South Carolina, USA
2Cancer Prevention and Control Program, University of South Carolina, Columbia, South Carolina, USA
Correspondence to Dr Jamie Ritchey; msritchey/at/hotmail.com
Received April 17, 2012; Accepted August 21, 2012.
Abstract
Objectives
Since sex hormone markers are metabolically linked, examining sex steroid hormones singly may account for inconsistent findings by age, race/ethnicity and body mass index (BMI) across studies. First, these markers were statistically combined into profiles to account for the metabolic relationship between markers. Then, the relationships between sex steroid hormone profiles and age, race/ethnicity and BMI were explored in multinomial logistic regression models.
Design
Cross-sectional survey.
Setting
The US Third National Health and Nutrition Examination Survey (NHANES III).
Participants
1538 Men, >17 years.
Primary outcome measure
Sex hormone profiles.
Results
Cluster analysis was used to identify four statistically determined profiles with Blom-transformed T, E, sex hormone binding globulin (SHBG), and 3-α diol G. We used these four profiles with multinomial logistic regression models to examine differences by race/ethnicity, age and BMI. Mexican American men >50 years were associated with the profile that had lowest T, E and 3-α diol G levels compared to other profiles (p<0.05). Non-Hispanic Black, overweight (25–29.9 kg/m2) and obese (>30 kg/m2) men were most likely to be associated with the cluster with the lowest SHBG (p<0.05).
Conclusion
The associations of sex steroid hormone profiles by race/ethnicity are novel, while the findings by age and BMI groups are largely consistent with observations from single hormone studies. Future studies should validate these hormone profile groups and investigate these profiles in relation to chronic diseases and certain cancers.
Keywords: Epidemiology
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