Rhee E J, Oh K W, Yun E J, Jung C H, Lee W Y, Kim S W, Baek K H, Kang M I, Park S W
Department of Internal Medicine, Sungkyunkwan University School of Medicine, Korea.
J Endocrinol Invest. 2006 Jul-Aug;29(7):613-8. doi: 10.1007/BF03344160.
Recently, klotho has been proposed as a link between cardiovascular diseases and premature aging, but the relationship between KLOTHO genes and cardiovascular risk factors, especially glucose metabolism, in humans is unclear.
We investigate the relationship between polymorphisms G395A in promoter and C1818T in exon 4 of the KLOTHO gene with glucose metabolism and cardiovascular risk factors in Korean women.
In 251 women (mean age 51.3+/-6.9 yr), body mass index (BMI), waist circumference, blood pressure, fasting plasma glucose, insulin and lipid profiles were measured. The genotyping of polymorphisms G395A in promoter and C1818T in exon 4 of the KLOTHO gene was performed by allelic discrimination using a 5' nuclease polymerase chain reaction assay.
Allele frequencies of G395A polymorphism was 0.829 for the G allele and 0.171 for the A allele and allele frequencies of C1818T polymorphism were 0.804 for the C allele and 0.196 for the T allele, both of which were in compliance with Hardy-Weinberg equilibrium and the two polymorphisms were in linkage disequilibrium (D'=0.43, p<0.01). Mean systolic blood pressure was significantly higher in A allele carriers of G395A polymorphism compared with non-carriers, and the significance was persistent even after adjustment for age and BMI. Mean fasting plasma glucose was significantly higher in T allele carriers of C1818T polymorphism compared with non-carriers, and the significance was persistent even after adjustment for age and BMI. Subjects without any minor allele from either single nucleotide polymorphisms (SNP) had significantly lower mean values for systolic, diastolic blood pressure and fasting plasma glucose levels compared with subjects with both minor allele from either SNP.
We observed that KLOTHO G395A polymorphism was associated with blood pressure and KLOTHO C1818T polymorphism was associated with glucose metabolism in Korean women. Further studies are needed to clarify this relationship.
最近,klotho被认为是心血管疾病与早衰之间的一个联系,但KLOTHO基因与人类心血管危险因素,尤其是糖代谢之间的关系尚不清楚。
我们研究韩国女性中KLOTHO基因启动子区G395A多态性和外显子4区C1818T多态性与糖代谢及心血管危险因素之间的关系。
对251名女性(平均年龄51.3±6.9岁)测量体重指数(BMI)、腰围、血压、空腹血糖、胰岛素和血脂水平。采用5'核酸酶聚合酶链反应分析通过等位基因鉴别对KLOTHO基因启动子区G395A多态性和外显子4区C1818T多态性进行基因分型。
G395A多态性的G等位基因频率为0.829,A等位基因频率为0.171;C1818T多态性的C等位基因频率为0.804,T等位基因频率为0.196,两者均符合哈迪-温伯格平衡,且这两个多态性处于连锁不平衡状态(D'=0.43,p<0.01)。G395A多态性的A等位基因携带者的平均收缩压显著高于非携带者,即使在调整年龄和BMI后该显著性仍然存在。C1818T多态性的T等位基因携带者的平均空腹血糖显著高于非携带者,即使在调整年龄和BMI后该显著性仍然存在。与携带任一单核苷酸多态性(SNP)的两个次要等位基因的受试者相比,未携带任一SNP次要等位基因的受试者的收缩压、舒张压和空腹血糖水平平均值显著更低。
我们观察到,在韩国女性中,KLOTHO G395A多态性与血压相关,KLOTHO C1818T多态性与糖代谢相关。需要进一步研究来阐明这种关系。