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波兰肥胖家族中候选基因的分析。

Analysis of candidate genes in Polish families with obesity.

作者信息

Malczewska-Malec Małgorzata, Wybranska Iwona, Leszczynska-Golabek Iwona, Partyka Lukasz, Hartwich Jadwiga, Jabrocka Agata, Kiec-Wilk Beata, Kwasniak Małgorzata, Motyka Marcin, Dembinska-Kiec Aldona

机构信息

Department of Clinical Biochemistry, The Jagiellonian University Medical College, Kraków, Poland.

出版信息

Clin Chem Lab Med. 2004 May;42(5):487-93. doi: 10.1515/CCLM.2004.083.

Abstract

This study analyzes the relationship between risk factors related to overweight/obesity, insulin resistance, lipid tolerance, hypertension, endothelial function and genetic polymorphisms associated with: i) appetite regulation (leptin, melanocortin-3-receptor (MCR-3), dopamine receptor 2 (D2R)); ii) adipocyte differentiation and insulin sensitivity (peroxisome proliferator-activated receptor-gamma2 (PPAR-gamma2), tumor necrosis factor-alpha (TNF-alpha)); iii) thermogenesis and free fatty acid (FFA) transport/catabolism (uncoupling protein-1 (UCP1), lipoprotein lipase (LPL), beta2- and beta3-adrenergic receptor (beta2AR, beta3AR), fatty acid transport protein-1 (FATP-1) and iv) lipoproteins (apoliprotein E (apoE), apo CIII). The 122 members of 40 obese Caucasian families from southern Poland participated in the study. The genotypes were analyzed by restriction fragment length polymorphism-polymerase chain reaction (RFLP-PCR) or by direct sequencing. Phenotypes related to obesity (body mass index (BMI), fat/lean body mass composition, waist-to-hip ratio (WHR)), fasting lipids, glucose, leptin and insulin, as well as insulin during oral glucose tolerance test (OGTT) (4 points within 2 hours) and during oral lipid tolerance test (OLTT) (5 points within 8 hours) were assessed. The insulin sensitivity indexes: homeostasis model assessment of insulin resistance, whole body insulin sensitivity index, hepatic insulin sensitivity and early secretory response to an oral glucose load (HOMA-IR, ISI-COMP, ISI-HOMA and DELTA) were calculated. The single gene mutations such as C105 T OB and Pro115 Gln PPAR-gamma2 linked to morbid obesity were not detected in our group. A weak correlation between obesity and certain gene polymorphisms was observed. Being overweight (25 < BMI > or = 30 kg/m2) significantly correlated with worse FFA tolerance in male PPAR-gamma2 12Pro, LPL-H (G) allele carriers. Insulin resistance was found in female PPAR-gamma2 Pro12, TNF-alpha (-308A) and LPL-H (G) allele carriers. Hypertension linked to the PPAR-gamma2 Pro allele carriers was characterized by high leptin output during OLTT. We conclude that the polymorphisms we investigated were weakly correlated with obesity but significantly modified the risk factors of the metabolic syndrome.

摘要

本研究分析了与超重/肥胖、胰岛素抵抗、脂质耐量、高血压、内皮功能相关的风险因素,以及与以下方面相关的基因多态性:i)食欲调节(瘦素、黑皮质素-3-受体(MCR-3)、多巴胺受体2(D2R));ii)脂肪细胞分化和胰岛素敏感性(过氧化物酶体增殖物激活受体-γ2(PPAR-γ2)、肿瘤坏死因子-α(TNF-α));iii)产热和游离脂肪酸(FFA)转运/分解代谢(解偶联蛋白-1(UCP1)、脂蛋白脂肪酶(LPL)、β2和β3肾上腺素能受体(β2AR、β3AR)、脂肪酸转运蛋白-1(FATP-1));iv)脂蛋白(载脂蛋白E(apoE)、载脂蛋白CIII)。来自波兰南部40个肥胖白种人家庭的122名成员参与了该研究。通过限制性片段长度多态性-聚合酶链反应(RFLP-PCR)或直接测序分析基因型。评估了与肥胖相关的表型(体重指数(BMI)、脂肪/瘦体重组成、腰臀比(WHR))、空腹血脂、血糖、瘦素和胰岛素,以及口服葡萄糖耐量试验(OGTT)(2小时内4个时间点)和口服脂质耐量试验(OLTT)(8小时内5个时间点)期间的胰岛素。计算了胰岛素敏感性指标:胰岛素抵抗的稳态模型评估、全身胰岛素敏感性指数、肝脏胰岛素敏感性和口服葡萄糖负荷后的早期分泌反应(HOMA-IR、ISI-COMP、ISI-HOMA和DELTA)。在我们的研究组中未检测到与病态肥胖相关的单基因突变,如C105T OB和Pro115Gln PPAR-γ2。观察到肥胖与某些基因多态性之间存在弱相关性。超重(25<BMI≥30kg/m2)与男性PPAR-γ2 12Pro、LPL-H(G)等位基因携带者较差的FFA耐量显著相关。在女性PPAR-γ2 Pro12、TNF-α(-308A)和LPL-H(G)等位基因携带者中发现了胰岛素抵抗。与PPAR-γ2 Pro等位基因携带者相关的高血压的特征是OLTT期间瘦素输出高。我们得出结论,我们研究的多态性与肥胖弱相关,但显著改变了代谢综合征的风险因素。

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