Association of leptin receptor gene polymorphisms and essential hypertension in a Chinese population

被引:23
作者
Gu, P. [1 ]
Jiang, W. [2 ]
Chen, M. [3 ]
Lu, B. [1 ]
Shao, J. [1 ]
Du, H. [1 ]
Jiang, S. [4 ]
机构
[1] Nanjing Gen Hosp Nanjing Command, Dept Endocrinol, Nanjing, Jiangsu, Peoples R China
[2] Jiangsu Prov Hosp Tradit Chinese Med, Dept Cardiol, Nanjing, Jiangsu, Peoples R China
[3] Nanjing Gen Hosp Nanjing Command, Dept Neurol, Nanjing, Jiangsu, Peoples R China
[4] Nanjing Gen Hosp Nanjing Command, Dept Cardiol, Nanjing, Jiangsu, Peoples R China
关键词
Essential hypertension; insulin resistance; leptin receptor gene; metabolic syndrome; single nucleotide polymorphisms; SYMPATHETIC-NERVE ACTIVATION; GLN223ARG POLYMORPHISM; INSULIN-RESISTANCE; BLOOD-PRESSURE; OBESITY; ADOLESCENTS; CHOLESTEROL; GLUCOSE; LOCUS; WOMEN;
D O I
10.3275/8238
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background: The leptin receptor (LEPR) is an important regulator of leptin activity and resistance. Several single nucleotide polymorphisms (SNP) of LEPR have been linked to diseases accompanying obesity and/or obesity-related diseases in different populations. However, the results from published studies remain inconsistent rather than conclusive. Aim: To investigate whether LEPR SNP are associated with essential hypertension and related metabolic traits in Chinese subjects. Materials and methods: A total of 544 Chinese patients with hypertension and 357 non-hypertensive subjects were screened. The genotypes of LEPR polymorphisms were determined by PCR-restriction fragment length polymorphism methods. Demographic and biochemical characteristics including waist circumference, waist-to-hip ratio, body mass index (BMI), lipids profiles, glucose metabolism, and leptin levels were obtained for analysis. Results: This case-control study showed associations between the frequencies of AA genotype and A allele of Gln223Arg and hypertension (p=0.029, p=0.002, respectively). Furthermore, the Gln223Arg polymorphism was significantly associated with plasma leptin levels (p < 0.001), while no correlations between Lys109Arg SNP and hypertension were found. Multivariate logistic regression analysis evidenced that A allele carriers of Gln223Arg (AA+AG) showed higher risks of hypertension than GG carriers after adjustment of age and sex (adjusted odds ratio: 1.549, 95% confidence interval: 1.031-2.036, p=0.035). BMI, fasting serum insulin, oral glucose tolernace test (OGTT)-2h glucose, serum leptin, as well as LDL-cholesterol (LDL-C) levels were also independent risk factors of hypertension in this population. In addition, significant associations were observed between the Gln223Arg and Lys109Arg SNP and serum total cholesterol, LDL-C, and fasting plasma glucose levels in hypertensive patients. Besides, A allele of Gln223Arg had raised diastolic blood pressure, compared with GG carriers (p=0.001). While variance of Lys109Arg was associated with waist-to-hip ratio, OGTT-2h glucose, and homeostasis model assessment of insulin resistance (p < 0.05). Conclusions: LEPR polymorphisms may be a marker for susceptibility to essential hypertension in Chinese subjects, and be involved in the development of several features including dyslipidemia and impaired glucose regulation in hypertension subjects. (J. Endocrinol. Invest. 35: 859-865, 2012) (c) 2012, Editrice Kurtis
引用
收藏
页码:859 / 865
页数:7
相关论文
共 34 条
[1]
Genetics of human hypertension [J].
Agarwal, A ;
Williams, GH ;
Fisher, NDL .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2005, 16 (03) :127-133
[2]
Pathophysiological role of leptin in obesity-related hypertension [J].
Aizawa-Abe, M ;
Ogawa, Y ;
Masuzaki, H ;
Ebihara, K ;
Satoh, N ;
Iwai, H ;
Matsuoka, N ;
Hayashi, T ;
Hosoda, K ;
Inoue, G ;
Yoshimasa, Y ;
Nakao, K .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (09) :1243-1252
[3]
LEPR p.Q223R Polymorphism Influences Plasma Leptin Levels and Body Mass Index in Tunisian Obese Patients [J].
Ben Ali, Samir ;
Kallel, Amani ;
Sediri, Yousra ;
Ftouhi, Bouchra ;
Feki, Moncef ;
Slimene, Hedia ;
Jemaa, Riadh ;
Kaabachi, Naziha .
ARCHIVES OF MEDICAL RESEARCH, 2009, 40 (03) :186-190
[4]
Obesity causes very low density lipoprotein clearance defects in low-density lipoprotein receptor-deficient mice [J].
Coenen, Kimberly R. ;
Gruen, Mamie L. ;
Hasty, Alyssa H. .
JOURNAL OF NUTRITIONAL BIOCHEMISTRY, 2007, 18 (11) :727-735
[5]
Leptin G-2548A and leptin receptor Q223R gene polymorphisms are not associated with obesity in Romanian subjects [J].
Constantin, Alina ;
Costache, Gabriela ;
Sima, Anca V. ;
Glavce, Cristiana S. ;
Vladica, Maria ;
Popov, Doina L. .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2010, 391 (01) :282-286
[6]
Intracerebroventricular leptin increases lumbar and renal sympathetic nerve activity and blood pressure in normal rats [J].
Dunbar, JC ;
Hu, YG ;
Lu, HQ .
DIABETES, 1997, 46 (12) :2040-2043
[7]
Expression of the functional leptin receptor mRNA in pancreatic islets and direct inhibitory action of leptin on insulin secretion [J].
Emilsson, V ;
Liu, YL ;
Cawthorne, MA ;
Morton, NM ;
Davenport, M .
DIABETES, 1997, 46 (02) :313-316
[8]
The Q223R polymorphism in LEPR is associated with obesity in Pacific Islanders [J].
Furusawa, Takuro ;
Naka, Izumi ;
Yamauchi, Taro ;
Natsuhara, Kazumi ;
Kimura, Ryosuke ;
Nakazawa, Minato ;
Ishida, Takafumi ;
Inaoka, Tsukasa ;
Matsumura, Yasuhiro ;
Ataka, Yuji ;
Nishida, Nao ;
Tsuchiya, Naoyuki ;
Ohtsuka, Ryutaro ;
Ohashi, Jun .
HUMAN GENETICS, 2010, 127 (03) :287-294
[9]
High-circulating leptin levels are associated with greater risk of hypertension in men independently of body mass and insulin resistance: Results of an eight-year follow-up study [J].
Galletti, F. ;
D'Elia, L. ;
Barba, G. ;
Siani, A. ;
Cappuccio, F. P. ;
Farinaro, E. ;
Iacone, R. ;
Russo, O. ;
De Palma, D. ;
Ippolito, R. ;
Strazzullo, P. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2008, 93 (10) :3922-3926
[10]
Association analysis of the Gln223Arg polymorphism in the human leptin receptor gene, and traits related to obesity in Mexican adolescents [J].
Guízar-Mendoza, JM ;
Amador-Licona, N ;
Flores-Martínez, SE ;
López-Cardona, MG ;
Ahuatzin-Trémary, R ;
Sánchez-Corona, J .
JOURNAL OF HUMAN HYPERTENSION, 2005, 19 (05) :341-346