Genetic polymorphisms of human transcription factor-7 like 2 (TCF7L2), β-defensin (DEFB1) and CD14 genes in nephrolithiasis patients

被引:2
作者
Mehdi, Wesen Adel [1 ]
Mehde, Atheer Awad [1 ]
Raus, Raha Ahmed [2 ]
Yusof, Faridah [2 ]
Abidin, Zaima Azira Zainal [3 ]
Ghazali, Hamid [4 ]
Abd Rahman, Azlina [5 ]
Ozacar, Mahmut [1 ,6 ]
机构
[1] Sakarya Univ, Biomed Magnet & Semicond Mat Applicat & Res Ctr B, TR-54187 Sakarya, Turkey
[2] Int Islamic Univ Malaysia, Dept Biotechnol Engn, Coll Engn, Kuala Lumpur 50728, Malaysia
[3] Int Islamic Univ Malaysia, Coll Sci, Kuantan 25200, Malaysia
[4] Hosp Tengku Ampuan Afzan, Dept Urol, Kuantan 25200, Malaysia
[5] Hosp Tengku Ampuan Afzan, Dept Pathol, Kuantan 25200, Malaysia
[6] Sakarya Univ, Sci & Arts Fac, Dept Chem, TR-54187 Sakarya, Turkey
关键词
TCF7L2; CD14; beta-Defensin; TYPE-2; DIABETES-MELLITUS; SOLUBLE CD14; HUMAN BETA-DEFENSIN-1; RS7903146; POLYMORPHISM; ASSOCIATION; RISK; VARIANTS; PROGRESSION; POPULATION; INFECTIONS;
D O I
10.1016/j.ijbiomac.2018.06.113
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: It is assumed that genetic factors play crucial role in nephrolithiasis. The present study was conducted to explore the role of Human Transcription Factor-7 like-2 (TCF7L2) beta-defensin (DEFBI) and CD14 gene polymorphism in development and progression of nephrolithiasis. Methods: The genotypes of TCF7L2, DEFB1 and CD14 polymorphism were determined in 240 nephrolithiasis patients and 240 healthy controls by restriction digestion method of PCR. The levels of serum TCF7L2, DEFB1, CD14, uric acid and other biochemical parameters were measured both in nephrolithiasis patients and healthy control. Results: The patients and control groups showed 30% and 50% 1654 AA DEFB1 genotype respectively. The Allele frequency in case of patient's group was 63.67% while in control group it was 3633%. The mean serum DEFB1 levels of the patients and control groups attained were 115.66 and 239.43 pg/mL respectively. The allele frequency of TCF7L2 in patients and controls were 44.17% and 70.0% for C-allele, 55.83% and 30.00% for T-allele respectively. The mean of serum TCF7L2 levels were significantly decreased in patients compared to control group. Conclusions: The present findings are first of its class that validates a considerable connection of DEFB1 and TCF7L2 gene polymorphisms with nephrolithiasis and could probably act as indicators to estimate the risk associated to nephrolithiasis. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:610 / 616
页数:7
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