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机构地区:[1]北京大学医学部营养与食品卫生学系,北京100083
出 处:《中国慢性病预防与控制》2002年第5期210-212,240,共4页Chinese Journal of Prevention and Control of Chronic Diseases
摘 要:目的了解脂蛋白脂酶 (L PL)基因 Pvu 位点多态性与肥胖代谢综合征的关系。方法对北京市西城区 2 11例超重 (BMI≥ 2 5 )和 93例体重正常的中老年人 (33~ 78岁 )进行 L PL- Pvu 位点多态性分析、体格检查及血生化指标检测。结果超重组与体重正常组 L PL- Pvu 位点基因型构成差异无显著性意义。L PL- Pvu 位点 (- /- )基因型携带者腰臀比低于 (+/+)基因型 ,HDL- C水平高于 (+/+)型 ,舒张压水平高于 (+/- )基因型 (P<0 .0 5 )。多因素分析显示腰臀比在 (+/+)、(+/- )和 (- /- )三种基因型间递减。结论 L PL基因 Pvu 位点 (- /- )基因型与腰臀比降低及 HDL- C水平升高有关 ,是肥胖代谢综合征的保护因素。Objective To investigate the relations of lipoprotein lipase gene-Pvu Ⅱ locus to obesity-related metabolism syndrome.Methods For all 211 overweight(BMI≥25) and 93 normal weight subjects (aged 33 to 81 years old),the polymorphism at LPL-Pvu Ⅱ locus were analyzed (PCR-RFLP),and physical examination,serum biochemical indexes were detected.Results There were no significant difference for the LPL-Pvu Ⅱ genotype distribution between overweight and control group.The levels of waist-hip ratio in (-/-) genotype carriers were significantly lower and HDL-C was higher than those in(+/+) genotype,and DBP higher than in (-/+)genotype(P<0.05).The multifactor analyses showed that WHR levels were gradually decreased in(+/+),(+/-)and(-/-)genotype.Conclusion The(-/-)genotype at LPL-Pvu Ⅱ locus was associated with decrease of WHR and increase of HDL-C,and it was a protective factor for obesity-related metabolism syndrome.
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