Literature DB >> 24483156

Insulin is inversely associated with bone mass, especially in the insulin-resistant population: the Korea and US National Health and Nutrition Examination Surveys.

Yong Jun Choi1, Dae Jung Kim, Yunhwan Lee, Yoon-Sok Chung.   

Abstract

BACKGROUND: Insulin is an important osteotropic hormone but may be negatively associated with bone mass after adjustment for body mass index in adolescent populations. However, the association between insulin and bone mass in adults remains unclear.
OBJECTIVE: The objective of the study was to investigate whether insulin was associated with bone mass in adults and, if so, whether the association was positive or negative.
DESIGN: This study had a cross-sectional design, using data from the Fourth Korea National Health and Nutrition Examination Survey (KNHANES) 2008-2009 and the US National Health and Nutrition Examination Survey (NHANES) 1999-2006.
SETTING: The setting for the study was the Korean and US population. PARTICIPANTS: A total of 7271 KNHANES and 3399 NHANES participants were included. MAIN OUTCOME MEASURES: Anthropometric parameters and bone mass data, fasting glucose and insulin, height, weight, and markers related to insulin resistance were measured.
RESULTS: After adjusting for confounding factors, there was an inverse relationship between insulin and total body bone mineral content in the KNHANES and NHANES subjects. In a stratified analysis, an association between insulin and bone mass was apparent, especially in the highest homeostatic model of assessment of insulin resistance quartile in the Korean subjects. However, this association was seen only in men in the US subjects.
CONCLUSIONS: There is an inverse relationship between insulin and total body bone mineral content after adjustment for confounding factors in Korean and US subjects, especially in the insulin-resistant population. This strongly suggests that the adverse influence of insulin on bone mass likely reflects the effects of other factors associated with insulin resistance rather than being a direct action of insulin itself.

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Year:  2014        PMID: 24483156     DOI: 10.1210/jc.2013-3346

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


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