Literature DB >> 19387627

Evidence suggesting a genetic contribution to kidney stone in northeastern Thai population.

Suchai Sritippayawan1, Sombat Borvornpadungkitti, Atchara Paemanee, Chagkrapan Predanon, Wattanachai Susaengrat, Duangporn Chuawattana, Nunghathai Sawasdee, Sirintra Nakjang, Suttikarn Pongtepaditep, Choochai Nettuwakul, Nanyawan Rungroj, Somkiat Vasuvattakul, Prida Malasit, Pa-thai Yenchitsomanus.   

Abstract

Genetic factor may play a role in the pathogenesis of kidney stone that is found in the northeastern (NE) Thai population. Herein, we report initial evidence suggesting genetic contribution to the disease in this population. We examined 1,034 subjects including 135 patients with kidney stone, 551 family members, and 348 villagers by radiography of kidney-ureter-bladder (KUB) and other methods, and also analyzed stones removed by surgical operations. One hundred and sixteen of 551 family members (21.05%) and 23 of the 348 villagers (6.61%) were affected with kidney stone. The relative risk (lambda(R)) of the disease among family members was 3.18. Calcium stones (whewellite, dahllite, and weddellite) were observed in about 88% of stones analyzed. Our data indicate familial aggregation of kidney stone in this population supporting that genetic factor should play some role in its pathogenesis. Genetic and genomic studies will be conducted to identify the genes associated with the disease.

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Year:  2009        PMID: 19387627     DOI: 10.1007/s00240-009-0189-1

Source DB:  PubMed          Journal:  Urol Res        ISSN: 0300-5623


  15 in total

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5.  Association of functional genetic variants in TFF1 and nephrolithiasis risk in a Chinese population.

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6.  Association between intelectin-1 variation and human kidney stone disease in northeastern Thai population.

Authors:  Thanakorn Pungsrinont; Choochai Nettuwakul; Nunghathai Sawasdee; Nanyawan Rungroj; Suchai Sritippayawan; Pa-Thai Yenchitsomanus
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7.  A whole genome SNP genotyping by DNA microarray and candidate gene association study for kidney stone disease.

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8.  Loss-of-function mutations of SCN10A encoding NaV1.8 α subunit of voltage-gated sodium channel in patients with human kidney stone disease.

Authors:  Choochai Nettuwakul; Oranud Praditsap; Nunghathai Sawasdee; Nanyawan Rungroj; Katesirin Ruamyod; Wattana B Watanapa; Mutita Junking; Sittideth Sangnual; Suchai Sritippayawan; Boonyarit Cheunsuchon; Duangporn Chuawattana; Santi Rojsatapong; Wipada Chaowagul; Sulayman D Dib-Hajj; Stephen G Waxman; Pa-Thai Yenchitsomanus
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  8 in total

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