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      Interaction between Sex and LDLR rs688 Polymorphism on Hyperlipidemia among Taiwan Biobank Adult Participants

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          Abstract

          Hyperlipidemia is one of the strong risk factors for ischemic heart disease. Using the Taiwan Biobank (TWB) database, we evaluated the risk of hyperlipidemia and its interaction with sex and rs688 polymorphism on the low-density lipoprotein receptor (LDLR) gene. Data collection in the biobank started in 2008 and is ongoing. Data analysis was performed on the participants’ data collected between 2008 and 2015. In general, 27.92% of the 9237 female participants and 32.65% of the 8690 male participants were identified with hyperlipidemia. Compared to the C/C genotype, C/T and T/T genotypes were not significant risk factors for hyperlipidemia (OR = 1.061, CI: 0.976–1.153 for C/T and OR = 1.052, CI: 0.845–1.309 for T/T genotype) in the general model. However, there was a significant interaction between sex and rs6888 on hyperlipidemia risk (p-interaction = 0.0321). With the male sex/CC genotype being the reference group, only the female sex/CT and T/T genotypes were closely associated with hyperlipidemia, with respective ORs of 1.153 (CI: 1.014–1.311) and 1.423 (CI: 1.056–1.917). Our data indicate that rs688 C/T and T/T genotypes may be associated with increased risk of hyperlipidemia in Taiwanese women. These findings may be relevant in lipid-modification therapy.

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          Epidemiology of Dyslipidemia in the Asia Pacific Region

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            Genetic determinants of inherited susceptibility to hypercholesterolemia – a comprehensive literature review

            Hypercholesterolemia is a strong determinant of mortality and morbidity associated with cardiovascular diseases and a major contributor to the global disease burden. Mutations in four genes (LDLR, APOB, PCSK9 and LDLRAP1) account for the majority of cases with familial hypercholesterolemia. However, a substantial proportion of adults with hypercholesterolemia do not have a mutation in any of these four genes. This indicates the probability of having other genes with a causative or contributory role in the pathogenesis of hypercholesterolemia and suggests a polygenic inheritance of this condition. Here in, we review the recent evidence of association of the genetic variants with hypercholesterolemia and the three lipid traits; total cholesterol (TC), HDL-cholesterol (HDL-C) and LDL-cholesterol (LDL-C), their biological pathways and the associated pathogenetic mechanisms. Nearly 80 genes involved in lipid metabolism (encoding structural components of lipoproteins, lipoprotein receptors and related proteins, enzymes, lipid transporters, lipid transfer proteins, and activators or inhibitors of protein function and gene transcription) with single nucleotide variants (SNVs) that are recognized to be associated with hypercholesterolemia and serum lipid traits in genome-wide association studies and candidate gene studies were identified. In addition, genome-wide association studies in different populations have identified SNVs associated with TC, HDL-C and LDL-C in nearly 120 genes within or in the vicinity of the genes that are not known to be involved in lipid metabolism. Over 90% of the SNVs in both these groups are located outside the coding regions of the genes. These findings indicates that there might be a considerable number of unrecognized processes and mechanisms of lipid homeostasis, which when disrupted, would lead to hypercholesterolemia. Knowledge of these molecular pathways will enable the discovery of novel treatment and preventive methods as well as identify the biochemical and molecular markers for the risk prediction and early detection of this common, yet potentially debilitating condition. Electronic supplementary material The online version of this article (doi:10.1186/s12944-017-0488-4) contains supplementary material, which is available to authorized users.
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              Diet and health trends in Taiwan: comparison of two nutrition and health surveys from 1993-1996 and 2005-2008.

              The availability of new food choices has increased dramatically in recent times, whilst increasingly sedentary lifestyles have reduced calorie intake requirements. The present study uses 24 hour dietary recall data, and biochemical and anthropometric measurements from the 1993-1996 and 2005-2008 Nutrition and Health Surveys in Taiwan (NAHSIT) to investigate trends in dietary habits, and cardiovascular and metabolic disease markers in Taiwanese persons aged 19 years and above. We found that dietary habits in Taiwan are changing, particularly in regards to intakes of cakes and sweets, and sugary drinks. Energy intakes in young people have increased, and combined with an increasingly sedentary lifestyle, this may have led to the increase in obesity and associated metabolic diseases. Large increases in the prevalence of the metabolic syndrome, diabetes, hypertriglyceridemia and gout have been observed. Fortunately, some positive dietary and behavioral changes have also been observed; including an increased avoidance of products made from animal fats and oils' and a concomitant increase in the use of vegetable oil. Intakes of fruit and vegetables, soy products, fish, whole grains, nuts and seeds have also increased; and intakes of red meat, carbohydrates and sodium containing foods have decreased. These positive dietary changes could explain the lack of large changes in the prevalence of hypertension and hypercholesterolemia, and the decrease in prevalence of hyperuricemia. Intake of dairy products remains low, and continues to be an important dietary issue in Taiwan.
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                Author and article information

                Journal
                Biomolecules
                Biomolecules
                biomolecules
                Biomolecules
                MDPI
                2218-273X
                05 February 2020
                February 2020
                : 10
                : 2
                : 244
                Affiliations
                [1 ]School of Medicine, Chung Shan Medical University, Taichung 40201, Taiwan; cvsliu0325@ 123456gmail.com
                [2 ]Department of Cardiovascular Surgery, Asia University Hospital, Taichung 40201, Taiwan
                [3 ]Department of Public Health and Institute of Public Health, Chung Shan Medical University, Taichung 40201, Taiwan wl@ 123456csmu.edu.tw (L.W.); sui0209@ 123456gmail.com (S.-Y.H.); dinoljc@ 123456csmu.edu.tw (C.-C.L.); tantohdisline@ 123456yahoo.com (D.M.T.)
                [4 ]Office of Physical Education, Chung Yuan Christian University, Taoyuan 32023, Taiwan; minchen@ 123456cycu.edu.tw
                [5 ]Division of Nephrology, Department of Internal Medicine, Chung Shan Medical University Hospital, Taichung 40201, Taiwan
                [6 ]Department of Medical Imaging, Chung Shan Medical University Hospital, Taichung City 40201, Taiwan
                Author notes
                [* ]Correspondence: chrcsmu@ 123456gmail.com (H.-R.C.); liawyp@ 123456csmu.edu.tw (Y.-P.L.); Tel.: +886-424-730-022 (ext. 11838) (H.-R.C.); Fax: +886-423-248-179 (Y.-P.L.)
                Author information
                https://orcid.org/0000-0002-3856-6734
                https://orcid.org/0000-0003-2046-4964
                Article
                biomolecules-10-00244
                10.3390/biom10020244
                7072141
                32033407
                047dc290-8038-42b3-8e1a-a420aa719f9c
                © 2020 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
                : 20 December 2019
                : 03 February 2020
                Categories
                Article

                hyperlipidemia,sex,biobank,polymorphism
                hyperlipidemia, sex, biobank, polymorphism

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