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      Association between Six CETP Polymorphisms and Metabolic Syndrome in Uyghur Adults from Xinjiang, China

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          Abstract

          Objective: To explore the association between CETP gene polymorphisms and metabolic syndrome (MS), as well as the relationship between the CETP gene polymorphisms and each component of MS. Methods: A total of 571 individuals which were randomly selected from 5692 Uyghur adults were subdivided into two groups, including 280 patients with MS and 291 control subjects, using the group-matching method after matching for gender. We detected CETP polymorphisms (rs5882, rs1800775, rs3764261, rs12149545, rs711752, and rs708272) by using the Snapshot method. Results: (1) Significant differences were found involving the frequency distribution of genotypes and alleles of rs1800775, rs3764261, rs12149545, rs711752, and rs708272 between the control and MS groups (all p < 0.05). (2) rs1800775, rs3764261, rs12149545, rs711752, and rs708272 polymorphisms were significantly related to the risk of MS (all p < 0.05). (3) The rs1800775 polymorphism was associated with high fasting blood glucose levels and low high density lipoprotein cholesterol (HDL-C); rs3764261 and rs12149545 polymorphisms were associated with all components of MS except high blood pressure; rs711752 and rs708272 polymorphisms were associated with low HDL-C (all p < 0.05). (4) Complete linkage disequilibrium (LD) was identified for two pairs of single nucleotide polymorphisms (SNPs) (rs3764261 and rs12149545 (D’ = 1.000, r 2 = 0.931), rs711752 and rs708272 (D’ = 1.000, r 2 = 0.996)). (5) The A-G-G-G-C ( p = 0.013, odds ratio [OR] = 0.622, 95% confidence interval [95% CI] = 0.427–0.906) and A-T-A-A-T ( p < 0.001, OR = 0.519, 95% CI = 0.386–0.697) haplotypes were more frequent in the control group than in the case group. Conclusions : The rs1800775, rs3764261, rs12149545, rs711752, and rs708272 polymorphisms of CETP were associated with MS and its components among the Uyghur ethnic group. Complete LD was found between two pairs of SNPs (rs3764261 and rs12149545, rs711752, and rs708272). The A-G-G-G-C and A-T-A-A-T haplotypes might be protective factors for MS.

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          Most cited references40

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          Obesity: Prevention and Managing the Global Epidemic. Report of a WHO Consultation

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            Metabolic syndrome: focus on dyslipidemia.

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              Genetic-epidemiological evidence on genes associated with HDL cholesterol levels: a systematic in-depth review.

              High-density lipoprotein (HDL) particles exhibit multiple antiatherogenic effects. They are key players in the reverse cholesterol transport which shuttles cholesterol from peripheral cells (e.g. macrophages) to the liver or other tissues. This complex process is thought to represent the basis for the antiatherogenic properties of HDL particles. The amount of cholesterol transported in HDL particles is measured as HDL cholesterol (HDLC) and is inversely correlated with the risk for coronary artery disease: an increase of 1mg/dL of HDLC levels is associated with a 2% and 3% decrease of the risk for coronary artery disease in men and women, respectively. Genetically determined conditions with high HDLC levels (e.g. familial hyperalphalipoproteinemia) often coexist with longevity, and higher HDLC levels were found among healthy elderly individuals. HDLC levels are under considerable genetic control with heritability estimates of up to 80%. The identification and characterization of genetic variants associated with HDLC concentrations can provide new insights into the background of longevity. This review provides an extended overview on the current genetic-epidemiological evidence from association studies on genes involved in HDLC metabolism. It provides a path through the jungle of association studies which are sometimes confusing due to the varying and sometimes erroneous names of genetic variants, positions and directions of associations. Furthermore, it reviews the recent findings from genome-wide association studies which have identified new genes influencing HDLC levels. The yet identified genes together explain only a small amount of less than 10% of the HDLC variance, which leaves an enormous room for further yet to be identified genetic variants. This might be accomplished by large population-based genome-wide meta-analyses and by deep-sequencing approaches on the identified genes. The resulting findings will probably result in a re-drawing and extension of the involved metabolic pathways of HDLC metabolism.
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                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Int J Environ Res Public Health
                Int J Environ Res Public Health
                ijerph
                International Journal of Environmental Research and Public Health
                MDPI
                1661-7827
                1660-4601
                18 June 2017
                June 2017
                : 14
                : 6
                : 653
                Affiliations
                Department of Public Health and Key Laboratory of Xinjiang Endemic and Ethnic Diseases of the Ministry of Education, Shihezi University School of Medicine, Shihezi 832002, China; sjzhx06@ 123456sina.com (H.H.); marulin@ 123456126.com (R.M.); guoheng@ 123456shzu.edu.cn (H.G.); hejia123.shihezi@ 123456163.com (J.H.); hyh6133@ 123456sina.com (Y.H.); murat08123@ 123456163.com (L.M.); erniu19880215@ 123456sina.com (Y.Y.); jiaojiaolong881202@ 123456163.com (J.M.); lishugang@ 123456ymail.com (S.L.); yfyxxzjy@ 123456126.com (J.Z.); 13399931625@ 123456163.com (Y.D.); zmberry@ 123456foxmail.com (M.Z.); niuqiang1214@ 123456163.com (Q.N.); liujiaming@ 123456shzu.edu.cn (J.L.)
                Author notes
                [* ]Correspondence: gsxshzu@ 123456sina.com ; Tel.: +86-180-0993-2625; Fax: +86-993-2057-153
                [†]

                These authors contributed equally to this work

                Article
                ijerph-14-00653
                10.3390/ijerph14060653
                5486339
                28629169
                bbdcc5f9-0464-4bca-aaa0-a0dc55de05e3
                © 2017 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 08 May 2017
                : 15 June 2017
                Categories
                Article

                Public health
                cetp gene,polymorphism,metabolic syndrome,uyghur
                Public health
                cetp gene, polymorphism, metabolic syndrome, uyghur

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