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Genetic variations in the leptin and leptin receptor genes are associated with type 2 diabetes mellitus and metabolic traits in the Korean female population
Author(s) -
Han HR,
Ryu HJ,
Cha HS,
Go MJ,
Ahn Y,
Koo BK,
Cho YM,
Lee HK,
Cho NH,
Shin C,
Shin HD,
Kimm K,
Kim HL,
Oh B,
Park KS
Publication year - 2008
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.2008.01033.x
Subject(s) - leptin , medicine , endocrinology , leptin receptor , type 2 diabetes mellitus , insulin resistance , body mass index , insulin , biology , type 2 diabetes , diabetes mellitus , obesity
Type 2 diabetes mellitus (T2DM) is a metabolic disorder that is characterized by insulin resistance and hyperglycemia. Leptin inhibits the glucose‐stimulated insulin secretion, and leptin receptors are present on β cells as well as on fat cells, thus enabling leptin to modulate both insulin secretion and action. Therefore, leptin ( LEP ) and leptin receptor ( LEPR ) genes could play a role in the regulation of glucose and insulin after an oral glucose load. For the association study of LEP and LEPR with T2DM and metabolic traits, 752 women from Seoul National University Hospital (SNUH data) and 532 women from the Korean Health and Genome Study (KHGS data) were selected. Using the SNUH data, we identified that LEP−632G>A and +4998A>C polymorphisms were marginally associated with T2DM, LEP + 4950G>A was significantly associated with several metabolic traits, and LEPR+5193G>A , +7187A>C , +27265G>A , +35861T>C , and +52289A>G showed strongly significant association with body mass index (BMI). We observed reproducibility of these results using the KHGS data; LEP+4950G>A and +4998A>C were significantly associated with systolic blood pressure and low‐density lipoprotein cholesterol level, respectively. In conclusion, we observed that several polymorphisms in LEPR that had previous reports of association with BMI were significantly replicated in our samples and newly found that some variations of LEP were associated with T2DM and metabolic traits.