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Cholesteryl Ester Transfer Protein Genetic Variants Associated with Risk for Type 2 Diabetes and Diabetic Kidney Disease in Taiwanese Population
Cholesteryl ester transfer protein (CETP) plays an important role in lipid metabolism. Low levels of high-density lipoprotein cholesterol (HDL-C) increase the risk of type 2 diabetes (T2D). This study investigated CETP gene variants to assess the risk of T2D and specific complications of diabetic ki...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826370/ https://www.ncbi.nlm.nih.gov/pubmed/31597401 http://dx.doi.org/10.3390/genes10100782 |
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author | Huang, Yu-Chuen Chen, Shih-Yin Liu, Shih-Ping Lin, Jane-Ming Lin, Hui-Ju Lei, Yu-Jie Chung, Yun-Chih Chen, Yu-Chi Wang, Yeh-Han Liao, Wen-Ling Tsai, Fuu-Jen |
author_facet | Huang, Yu-Chuen Chen, Shih-Yin Liu, Shih-Ping Lin, Jane-Ming Lin, Hui-Ju Lei, Yu-Jie Chung, Yun-Chih Chen, Yu-Chi Wang, Yeh-Han Liao, Wen-Ling Tsai, Fuu-Jen |
author_sort | Huang, Yu-Chuen |
collection | PubMed |
description | Cholesteryl ester transfer protein (CETP) plays an important role in lipid metabolism. Low levels of high-density lipoprotein cholesterol (HDL-C) increase the risk of type 2 diabetes (T2D). This study investigated CETP gene variants to assess the risk of T2D and specific complications of diabetic kidney disease (DKD) and diabetic retinopathy. Towards this, a total of 3023 Taiwanese individuals (1383 without T2D, 1640 with T2D) were enrolled in this study. T2D mice (+Lepr(db)/+Lepr(db), db/db) were used to determine CETP expression in tissues. The A-alleles of rs3764261, rs4783961, and rs1800775 variants were found to be independently associated with 2.86, 1.71, and 0.91 mg/dL increase in HDL-C per allele, respectively. In addition, the A-allele of rs4783961 was significantly associated with a reduced T2D risk (odds ratio (OR), 0.82; 95% confidence interval (CI), 0.71–0.96)), and the A-allele of rs1800775 was significantly related to a lowered DKD risk (OR, 0.78; 95% CI, 0.64–0.96). CETP expression was significantly decreased in the T2D mice kidney compared to that in the control mice (T2D mice, 0.16 ± 0.01 vs. control mice, 0.21 ± 0.02; p = 0.02). These collective findings indicate that CETP variants in the promoter region may affect HDL-C levels. Taiwanese individuals possessing an allele associated with higher HDL-C levels had a lower risk of T2D and DKD. |
format | Online Article Text |
id | pubmed-6826370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-68263702019-11-18 Cholesteryl Ester Transfer Protein Genetic Variants Associated with Risk for Type 2 Diabetes and Diabetic Kidney Disease in Taiwanese Population Huang, Yu-Chuen Chen, Shih-Yin Liu, Shih-Ping Lin, Jane-Ming Lin, Hui-Ju Lei, Yu-Jie Chung, Yun-Chih Chen, Yu-Chi Wang, Yeh-Han Liao, Wen-Ling Tsai, Fuu-Jen Genes (Basel) Article Cholesteryl ester transfer protein (CETP) plays an important role in lipid metabolism. Low levels of high-density lipoprotein cholesterol (HDL-C) increase the risk of type 2 diabetes (T2D). This study investigated CETP gene variants to assess the risk of T2D and specific complications of diabetic kidney disease (DKD) and diabetic retinopathy. Towards this, a total of 3023 Taiwanese individuals (1383 without T2D, 1640 with T2D) were enrolled in this study. T2D mice (+Lepr(db)/+Lepr(db), db/db) were used to determine CETP expression in tissues. The A-alleles of rs3764261, rs4783961, and rs1800775 variants were found to be independently associated with 2.86, 1.71, and 0.91 mg/dL increase in HDL-C per allele, respectively. In addition, the A-allele of rs4783961 was significantly associated with a reduced T2D risk (odds ratio (OR), 0.82; 95% confidence interval (CI), 0.71–0.96)), and the A-allele of rs1800775 was significantly related to a lowered DKD risk (OR, 0.78; 95% CI, 0.64–0.96). CETP expression was significantly decreased in the T2D mice kidney compared to that in the control mice (T2D mice, 0.16 ± 0.01 vs. control mice, 0.21 ± 0.02; p = 0.02). These collective findings indicate that CETP variants in the promoter region may affect HDL-C levels. Taiwanese individuals possessing an allele associated with higher HDL-C levels had a lower risk of T2D and DKD. MDPI 2019-10-08 /pmc/articles/PMC6826370/ /pubmed/31597401 http://dx.doi.org/10.3390/genes10100782 Text en © 2019 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/). |
spellingShingle | Article Huang, Yu-Chuen Chen, Shih-Yin Liu, Shih-Ping Lin, Jane-Ming Lin, Hui-Ju Lei, Yu-Jie Chung, Yun-Chih Chen, Yu-Chi Wang, Yeh-Han Liao, Wen-Ling Tsai, Fuu-Jen Cholesteryl Ester Transfer Protein Genetic Variants Associated with Risk for Type 2 Diabetes and Diabetic Kidney Disease in Taiwanese Population |
title | Cholesteryl Ester Transfer Protein Genetic Variants Associated with Risk for Type 2 Diabetes and Diabetic Kidney Disease in Taiwanese Population |
title_full | Cholesteryl Ester Transfer Protein Genetic Variants Associated with Risk for Type 2 Diabetes and Diabetic Kidney Disease in Taiwanese Population |
title_fullStr | Cholesteryl Ester Transfer Protein Genetic Variants Associated with Risk for Type 2 Diabetes and Diabetic Kidney Disease in Taiwanese Population |
title_full_unstemmed | Cholesteryl Ester Transfer Protein Genetic Variants Associated with Risk for Type 2 Diabetes and Diabetic Kidney Disease in Taiwanese Population |
title_short | Cholesteryl Ester Transfer Protein Genetic Variants Associated with Risk for Type 2 Diabetes and Diabetic Kidney Disease in Taiwanese Population |
title_sort | cholesteryl ester transfer protein genetic variants associated with risk for type 2 diabetes and diabetic kidney disease in taiwanese population |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6826370/ https://www.ncbi.nlm.nih.gov/pubmed/31597401 http://dx.doi.org/10.3390/genes10100782 |
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