The causal effects of alcohol on lipoprotein subfraction and triglyceride levels using a Mendelian randomization analysis: The Nagahama study

被引:21
作者
Tabara, Yasuharu [1 ]
Arai, Hidenori [2 ]
Hirao, Yuhko [3 ]
Takahashi, Yoshimitsu [4 ]
Setoh, Kazuya [1 ]
Kawaguchi, Takahisa [1 ]
Kosugi, Shinji [5 ]
Ito, Yasuki [3 ]
Nakayama, Takeo [4 ]
Matsuda, Fumihiko [1 ]
机构
[1] Kyoto Univ, Grad Sch Med, Ctr Genom Med, Kyoto, Japan
[2] Natl Ctr Geriatr & Gerontol, Obu, Japan
[3] Denka Seiken Co Ltd, Ctr Res & Dev, Tokyo, Japan
[4] Kyoto Univ, Sch Publ Hlth, Dept Hlth Informat, Kyoto, Japan
[5] Kyoto Univ, Sch Publ Hlth, Dept Med Eth & Med Genet, Kyoto, Japan
关键词
High-density lipoprotein; Low-density lipoprotein; Lipoprotein subfractions; Alcohol consumption; Mendelian randomization analysis; HIGH-DENSITY-LIPOPROTEIN; CARDIOVASCULAR RISK-FACTORS; ESTER TRANSFER PROTEIN; BLOOD-PRESSURE; CHOLESTEROL LEVELS; HOMOGENEOUS ASSAY; LIPID LEVELS; CONSUMPTION; PLASMA; ASSOCIATION;
D O I
10.1016/j.atherosclerosis.2016.12.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Light-to-moderate alcohol consumption may increase circulating high-density lipoprotein cholesterol (HDL-C) levels and decrease low-density lipoprotein cholesterol (LDL-C) levels. However, the effect of alcohol on biologically important lipoprotein subfractions remains largely unknown. Here we aimed to clarify the effects of alcohol on lipoprotein subfractions using a Mendelian randomization analysis. Methods: The study subjects consisted of 8364 general Japanese individuals. The rs671 polymorphism in aldehyde dehydrogenase 2 gene, a rate-controlling enzyme of alcohol metabolism, was used as an instrumental variable. Lipoprotein subfractions were measured by a homogeneous assay. Results: The biologically active *1 allele of the ALDH2 genotype was strongly associated with alcohol consumption in men (p < 0.001). In a regression analysis adjusted for possible covariates, the *1 allele was positively associated with HDL-C even in a sub-analysis for HDL subfractions (HDL2-C: beta = 0.082, p < 0.001; HDL3-C: beta = 0.195, p < 0.001). In contrast, the *1 allele was inversely associated with total LDLC levels (beta = -0.049, p = 0.008), while its association with large-buoyant LDL-C (beta = -0.124, p < 0.001) and small-dense LDL-C (beta = 0.069, p < 0.001) was opposite. Therefore, the ratio of small-dense LDL to large-buoyant LDL exhibited a linear increase with the number of *1 alleles carried (beta = 0.127, p < 0.001). Furthermore, the *1 allele was inversely associated with triglyceride levels in an analysis adjusted for LDL subfractions (beta = -0.097, p < 0.001), but not for the total LDL (beta = 0.014, beta = 0.410). Conclusions: Alcohol may increase HDL-C levels irrespective of the particle size. Moreover, alcohol may decrease the total LDL-C, although the proportion of atherogenic small-dense LDL-C increased partially due to a potential inter-relationship with decreased triglyceride levels. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:22 / 28
页数:7
相关论文
共 38 条
[1]   The inherent accuracy of 1H NMR spectroscopy to quantify plasma lipoproteins is subclass dependent [J].
Ala-Korpela, Mika ;
Lankinen, Niko ;
Salminen, Aino ;
Suna, Teemu ;
Soininen, Pasi ;
Laatikainen, Reino ;
Ingman, Petri ;
Jauhiainen, Matti ;
Taskinen, Marja-Riitta ;
Heberger, Karoly ;
Kaski, Kimmo .
ATHEROSCLEROSIS, 2007, 190 (02) :352-358
[2]  
Amamoto K, 2002, HYPERTENS RES, V25, P857
[3]  
Arai H., 2012, J ATHEROSCLER THROMB, V20, P195
[4]   Mendelian randomization studies: a review of the approaches used and the quality of reporting [J].
Boef, Anna G. C. ;
Dekkers, Olaf M. ;
le Cessie, Saskia .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2015, 44 (02) :496-511
[5]   Effects of ethanol intake on lipoproteins and atherosclerosis [J].
Brinton, Eliot A. .
CURRENT OPINION IN LIPIDOLOGY, 2010, 21 (04) :346-351
[6]   Alcohol intake and cardiovascular risk factors: A Mendelian randomisation study [J].
Cho, Yoonsu ;
Shin, So-Youn ;
Won, Sungho ;
Relton, Caroline L. ;
Smith, George Davey ;
Shin, Min-Jeong .
SCIENTIFIC REPORTS, 2015, 5
[7]   ALCOHOL INTAKE AND SERUM-LIPIDS IN A JAPANESE POPULATION [J].
CHOUDHURY, SR ;
UESHIMA, H ;
KITA, Y ;
KOBAYASHI, KM ;
OKAYAMA, A ;
YAMAKAWA, M ;
HIRAO, Y ;
ISHIKAWA, M ;
MIYOSHI, Y .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 1994, 23 (05) :940-947
[8]   ALCOHOL INTAKE IN RELATION TO DIET AND OBESITY IN WOMEN AND MEN [J].
COLDITZ, GA ;
GIOVANNUCCI, E ;
RIMM, EB ;
STAMPFER, MJ ;
ROSNER, B ;
SPEIZER, FE ;
GORDIS, E ;
WILLETT, WC .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1991, 54 (01) :49-55
[9]   Genetic polymorphisms of ADH1B, ADH1C and ALDH2, alcohol consumption, and the risk of gastric cancer: the Japan Public Health Center-based prospective study [J].
Hidaka, Akihisa ;
Sasazuki, Shizuka ;
Matsuo, Keitaro ;
Ito, Hidemi ;
Sawada, Norie ;
Shimazu, Taichi ;
Yamaji, Taiki ;
Iwasaki, Motoki ;
Inoue, Manami ;
Tsugane, Shoichiro .
CARCINOGENESIS, 2015, 36 (02) :223-231
[10]   POLYDISPERSE LOW-DENSITY LIPOPROTEINS IN HYPERALPHALIPOPROTEINEMIC CHRONIC ALCOHOL DRINKERS IN ASSOCIATION WITH MARKED REDUCTION OF CHOLESTERYL ESTER TRANSFER PROTEIN-ACTIVITY [J].
HIRANO, K ;
MATSUZAWA, Y ;
SAKAI, N ;
HIRAOKA, H ;
NOZAKI, S ;
FUNAHASHI, T ;
YAMASHITA, S ;
KUBO, M ;
TARUI, S .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1992, 41 (12) :1313-1318