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KMID : 1200020190430060867
Diabetes & Metabolism Journal
2019 Volume.43 No. 6 p.867 ~ p.878
The Relationship between Thyroid Function and Different Obesity Phenotypes in Korean Euthyroid Adults
Kim Jeong-Mi

Kim Bo-Hyun
Lee Hyun-Gi
Kim Eun-Heui
Kim Mi-Jin
Kim Jong-Ho
Jeon Yun-Kyung
Kim Sang-Soo
Kim In-Joo
Kim Yong-Ki
Abstract
Background: Thyroid disease and metabolic syndrome are both associated with cardiovascular disease. The aim of this study was to investigate the correlation between thyroid hormones and obesity sub-phenotypes using nationwide data from Korea, a country known to be iodine replete.

Methods: This study was based on data obtained from the sixth Korea National Health and Nutrition Examination Survey, administered from 2013 to 2015. A total of 13,873 participants aged ¡Ã19 years were included, and classified into four groups: metabolically healthy non-obesity (MHNO), metabolically healthy obesity (MHO), metabolically unhealthy non-obesity (MUNO), and metabolically unhealthy obesity (MUO) by body fat on the basis of body mass index and metabolic health.

Results: At baseline, serum free thyroxine (fT4) values were significantly higher in the MHNO phenotype (MHNO, 1.27¡¾0.01 ng/dL; MHO, 1.25¡¾0.01 ng/dL; MUNO, 1.24¡¾0.01 ng/dL; MUO, 1.24¡¾0.01 ng/dL, P<0.001) in total study population. However, this significant association no longer remained after adjustment for age, urine iodine concentration, and smoking (P=0.085). After adjustment for confounders, statistically significant association was observed between lower thyroid stimulating hormone (TSH) and MHNO phenotype (P=0.044). In men participants (not women), higher fT4 values were significantly associated with MHNO phenotype (P<0.001). However, no significant association was observed between thyroid function (TSH or fT4) and obesity phenotypes in groups classified by age (cutoff age of 55 years).

Conclusion: Although there was a difference by age and sex, we found that the decrease of TSH and the increase of fT4 values were associated with MHNO.
KEYWORD
Metabolic syndrome, Obesity, Phenotype, Sex, Thyroid hormones
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