Serum haptoglobin correlates positively with cholesterol and triglyceride concentrations in an obese Mongolian population

被引:7
作者
Soejima, Mikiko [1 ]
Munkhtulga, Lkhagvasuren [2 ]
Furukawa, Kyoji [3 ]
Iwamoto, Sadahiko [4 ]
Koda, Yoshiro [1 ]
机构
[1] Kurume Univ, Dept Forens Med, Sch Med, Kurume, Fukuoka, Japan
[2] Hlth Sci Univ Mongolia, Biomed Sch, Dept Pathophysiol, Ulaanbaatar, Mongolia
[3] Kurume Univ, Biostat Ctr, Kurume, Fukuoka, Japan
[4] Jichi Med Univ, Ctr Community Med, Div Human Genet, Shimotsuke, Tochigi, Japan
关键词
Cholesterol; Polymorphisms; Triglyceride; Obesity; Haptoglobin; APOLIPOPROTEIN-E; GENE DELETION; POLYMORPHISM; HP; ASSOCIATION; ALLELE; LIPIDS; LEVEL; BINDS;
D O I
10.1016/j.cca.2020.03.003
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Recent studies revealed that several genetic polymorphisms of haptoglobin gene (HP) and the haptoglobin-related protein gene (HPR) associated not only with haptoglobin (HP) but total, non-HDL, and/or LDL cholesterol concentrations in various populations. Methods: Association between serum HP concentrations and polymorphisms of HP and the HPR gene, or anthropometric and metabolic factors were examined in Mongolian participants (n = 927) using linear regression analyses. Results: The association of HP and HPR polymorphisms with serum HP concentration but not serum lipids concentrations was observed. However, subgroup analysis revealed that the association of HP and HPR polymorphisms with serum HP concentration was weakened in subgroup of obese (BMI = 30) subjects and positive correlations between serum HP and non-HDL cholesterol, HDL cholesterol or triglyceride concentrations were observed in the obese subjects as compared with in subgroups of normal weight (BMI < 25) and overweight (25 = BMI < 30) subjects. Conclusion: The degree of obesity strongly affects the relationships between serum HP concentrations and several genetic, anthropometric and metabolic factors. These results suggested that we need to take into account the degree of obesity when considering the HP polymorphisms as predictive markers for clinical states.
引用
收藏
页码:176 / 182
页数:7
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