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Relationship of sex steroid hormones with bone mineral density of the lumbar spine in adult men

AIMS: To examine the relationship of sex steroid hormones with osteopenia in a nationally representative sample of men in the USA. METHODS: Data on bone mineral density (BMD), serum sex hormones, dairy consumption, smoking status, and body composition were available for 806 adult male participants o...

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Autores principales: Guebeli, Alissa, Platz, Elizabeth A., Paller, Channing J, McGlynn, Katherine A., Rohrmann, Sabine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229310/
https://www.ncbi.nlm.nih.gov/pubmed/32435466
http://dx.doi.org/10.1302/2046-3758.93.BJR-2019-0141.R1
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author Guebeli, Alissa
Platz, Elizabeth A.
Paller, Channing J
McGlynn, Katherine A.
Rohrmann, Sabine
author_facet Guebeli, Alissa
Platz, Elizabeth A.
Paller, Channing J
McGlynn, Katherine A.
Rohrmann, Sabine
author_sort Guebeli, Alissa
collection PubMed
description AIMS: To examine the relationship of sex steroid hormones with osteopenia in a nationally representative sample of men in the USA. METHODS: Data on bone mineral density (BMD), serum sex hormones, dairy consumption, smoking status, and body composition were available for 806 adult male participants of the cross-sectional National Health and Nutrition Examination Survey (NHANES, 1999-2004). We estimated associations between quartiles of total and estimated free oestradiol (E2) and testosterone (T) and osteopenia (defined as 1 to 2.5 SD below the mean BMD for healthy 20- to 29-year-old men) by applying sampling weights and using multivariate-adjusted logistic regression. We then estimated the association between serum hormone concentrations and osteopenia by percentage of body fat, frequency of dairy intake, cigarette smoking status, age, and race/ethnicity. RESULTS: Men in the lowest quartile of total E2 concentrations (< 21.52 pg/ml) had greater odds of osteopenia compared with men in the highest quartile (odds ratio (OR) 2.29, 95% confidence interval (CI) 1.11 to 4.73; p-trend = 0.030). Total and free T were not associated with osteopenia. Low total E2 concentrations were associated with greater odds of osteopenia among non-daily dairy consumers (p-trend = 0.046), current or former smokers (p-trend = 0.032), and younger men (p-trend = 0.031). No differences were observed by race/ethnicity and obesity. CONCLUSION: In this nationally representative study of the USA, men with lower total E2 were more likely to have osteopenia, which was particularly evident among younger men, men with less-than-daily dairy consumption, and current or former smokers. Cite this article: Bone Joint Res. 2020;9(3):139–145.
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spelling pubmed-72293102020-05-20 Relationship of sex steroid hormones with bone mineral density of the lumbar spine in adult men Guebeli, Alissa Platz, Elizabeth A. Paller, Channing J McGlynn, Katherine A. Rohrmann, Sabine Bone Joint Res Biomaterials AIMS: To examine the relationship of sex steroid hormones with osteopenia in a nationally representative sample of men in the USA. METHODS: Data on bone mineral density (BMD), serum sex hormones, dairy consumption, smoking status, and body composition were available for 806 adult male participants of the cross-sectional National Health and Nutrition Examination Survey (NHANES, 1999-2004). We estimated associations between quartiles of total and estimated free oestradiol (E2) and testosterone (T) and osteopenia (defined as 1 to 2.5 SD below the mean BMD for healthy 20- to 29-year-old men) by applying sampling weights and using multivariate-adjusted logistic regression. We then estimated the association between serum hormone concentrations and osteopenia by percentage of body fat, frequency of dairy intake, cigarette smoking status, age, and race/ethnicity. RESULTS: Men in the lowest quartile of total E2 concentrations (< 21.52 pg/ml) had greater odds of osteopenia compared with men in the highest quartile (odds ratio (OR) 2.29, 95% confidence interval (CI) 1.11 to 4.73; p-trend = 0.030). Total and free T were not associated with osteopenia. Low total E2 concentrations were associated with greater odds of osteopenia among non-daily dairy consumers (p-trend = 0.046), current or former smokers (p-trend = 0.032), and younger men (p-trend = 0.031). No differences were observed by race/ethnicity and obesity. CONCLUSION: In this nationally representative study of the USA, men with lower total E2 were more likely to have osteopenia, which was particularly evident among younger men, men with less-than-daily dairy consumption, and current or former smokers. Cite this article: Bone Joint Res. 2020;9(3):139–145. 2020-05-16 /pmc/articles/PMC7229310/ /pubmed/32435466 http://dx.doi.org/10.1302/2046-3758.93.BJR-2019-0141.R1 Text en © 2020 Author(s) et al Open Access This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (CC BY-NC-ND 4.0) licence, which permits the copying and redistribution of the work only, and provided the original author and source are credited. See https://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Biomaterials
Guebeli, Alissa
Platz, Elizabeth A.
Paller, Channing J
McGlynn, Katherine A.
Rohrmann, Sabine
Relationship of sex steroid hormones with bone mineral density of the lumbar spine in adult men
title Relationship of sex steroid hormones with bone mineral density of the lumbar spine in adult men
title_full Relationship of sex steroid hormones with bone mineral density of the lumbar spine in adult men
title_fullStr Relationship of sex steroid hormones with bone mineral density of the lumbar spine in adult men
title_full_unstemmed Relationship of sex steroid hormones with bone mineral density of the lumbar spine in adult men
title_short Relationship of sex steroid hormones with bone mineral density of the lumbar spine in adult men
title_sort relationship of sex steroid hormones with bone mineral density of the lumbar spine in adult men
topic Biomaterials
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7229310/
https://www.ncbi.nlm.nih.gov/pubmed/32435466
http://dx.doi.org/10.1302/2046-3758.93.BJR-2019-0141.R1
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