Vitamin D receptor gene (VDR) polymorphisms and the urolithiasis risk: an updated meta-analysis based on 20 case-control studies

被引:21
作者
Liu, Wentao [1 ]
Chen, Minfeng [1 ]
Li, Mengjun [2 ]
Ma, Hong [3 ]
Tong, Shiyu [1 ]
Lei, Ye [1 ]
Qi, Lin [1 ]
机构
[1] Cent S Univ, Xiangya Hosp, Dept Urol, Changsha, Hunan, Peoples R China
[2] Cent S Univ, Xiangya Hosp 2, Dept Neurosurg, Changsha, Hunan, Peoples R China
[3] Cent S Univ, Xiangya Hosp 2, Dept Spine Surg, Changsha, Hunan, Peoples R China
关键词
Vitamin D receptor; Polymorphisms; Urolithiasis; Meta-analysis; HARDY-WEINBERG EQUILIBRIUM; OXALATE STONE DISEASE; BONE-MINERAL DENSITY; FOK-I POLYMORPHISM; KIDNEY-STONES; CALCIUM NEPHROLITHIASIS; MOLECULAR ASSOCIATION; CLINICAL-TRIALS; EXCRETION; CHILDREN;
D O I
10.1007/s00240-013-0619-y
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Vitamin D receptor (VDR) plays a key role in calcium metabolism, and is closely related to urinary stone formation (urolithiasis). Previous studies have investigated the associations between VDR single nucleotide polymorphisms (SNPs) (polymorphisms at BsmI, ApaI, FokI, or TaqI cutting sites) and urolithiasis in different populations. However, the results remain inconsistent and controversial. Therefore, meta-analysis was performed to evaluate these associations. Twenty studies that investigated the associations between VDR SNPs and urolithiasis were retrieved. Odds ratios (ORs) with 95 % confidence intervals (CIs) were calculated under the most appropriate genetic model. The TaqI polymorphism was associated with an increased risk of urolithiasis (tt + Tt vs. TT: OR = 1.253; 95 % CI = 1.033-1.520, p = 0.022, I (2) = 0), whereas the ApaI, BsmI, and FokI polymorphisms were not. Stratifying for ethnicity, a slightly increased risk was found among Asians as compared to Whites (OR 1.263, 1.232, respectively, p < 0.01). Deviation from Hardy-Weinberg equilibrium (HWE) was the major source of heterogeneity. In summary, this updated meta-analysis suggests the TaqI polymorphism is associated with urolithiasis risk, whereas BsmI, ApaI, and FokI polymorphisms are not.
引用
收藏
页码:45 / 52
页数:8
相关论文
共 45 条
  • [11] METAANALYSIS IN CLINICAL-TRIALS
    DERSIMONIAN, R
    LAIRD, N
    [J]. CONTROLLED CLINICAL TRIALS, 1986, 7 (03): : 177 - 188
  • [12] A polymorphism of the osteopontin gene is related to urinary calcium stones
    Gao, B
    Yasui, T
    Okada, A
    Tozawa, K
    Hayashi, Y
    Kohri, K
    [J]. JOURNAL OF UROLOGY, 2005, 174 (04) : 1472 - 1476
  • [13] A twin study of genetic and dietary influences on nephrolithiasis: A report from the Vietnam Era Twin (VET) Registry
    Goldfarb, DS
    Fischer, ME
    Keich, Y
    Goldberg, J
    [J]. KIDNEY INTERNATIONAL, 2005, 67 (03) : 1053 - 1061
  • [14] GENETIC-FACTORS IN CALCIUM-OXALATE STONE DISEASE
    GOODMAN, HO
    HOLMES, RP
    ASSIMOS, DG
    [J]. JOURNAL OF UROLOGY, 1995, 153 (02) : 301 - 307
  • [15] Vitamin D receptor gene polymorphisms in patients with urolithiasis
    Gunes, S
    Bilen, CY
    Kara, N
    Asci, R
    Bagci, H
    Yilmaz, AF
    [J]. UROLOGICAL RESEARCH, 2006, 34 (01): : 47 - 52
  • [17] Detection of genotyping errors by Hardy-Weinberg equilibrium testing
    Hosking, L
    Lumsden, S
    Lewis, K
    Yeo, A
    McCarthy, L
    Bansal, A
    Riley, J
    Purvis, I
    Xu, CF
    [J]. EUROPEAN JOURNAL OF HUMAN GENETICS, 2004, 12 (05) : 395 - 399
  • [18] Familial calcium stone disease:: TaqI polymorphism and the vitamin D receptor
    Jackman, SV
    Kibel, AS
    Ovuworie, CA
    Moore, RG
    Kavoussi, LR
    Jarrett, TW
    [J]. JOURNAL OF ENDOUROLOGY, 1999, 13 (04) : 313 - 316
  • [19] Association of vitamin D receptor-gene (FokI), polymorphism with calcium oxalate nephrolithiasis
    Kumar, H
    Kumar, A
    Kapoor, R
    Mittal, RD
    [J]. JOURNAL OF ENDOUROLOGY, 2005, 19 (01) : 111 - 115
  • [20] Vitamin D Receptor Genetic Polymorphisms and the Risk of Urolithiasis: A Meta-Analysis
    Lin, Yiwei
    Mao, Qiqi
    Zheng, Xiangyi
    Chen, Hong
    Yang, Kai
    Xie, Liping
    [J]. UROLOGIA INTERNATIONALIS, 2011, 86 (03) : 249 - 255