Document Detail


A high prevalence of Gitelman's syndrome mutations in Japanese.
MedLine Citation:
PMID:  15198479     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Although Gitelman's syndrome (GS) is considered a rare disorder, it is an autosomal recessive phenotype and the frequency of heterozygote subjects might be higher than suspected. The purpose of this study was to assess the prevalence of GS in Japanese and the effects of heterozygous GS mutations on blood pressure levels. We used the TaqMan system to detect 9 Gitelman's syndrome mutations in SLC12A3 that have been reported in Japanese. We then conducted association studies between these mutations and blood pressure in 1,852 subjects recruited from the Suita study, representing the general population in Japan. Among these 1,852 subjects, we detected the T180K, A569V, L623P, R642C, and L849H heterozygote genotypes in 56, 14, 1, 1, and 47 subjects, respectively. The overall frequency of GS mutations was (56+14+1+1+47) / (1,852 x 2) = 0.0321, which was much higher than suspected. This means we should expect to find one subject with a heterozygous GS mutation among 15.6 Japanese or that we should find 10.3 GS subjects among 10,000 Japanese. Although the blood pressure levels of subjects heterozygous for the T180K, A569V, or L849H genotype were not significantly different from those of wild-type subjects, urine pH in subjects with GS mutations was significantly higher than that in subjects without mutations. In conclusion, GS could be one of the major causes of low blood pressure in Japanese.
Authors:
Naomi Tago; Yoshihiro Kokubo; Nozomu Inamoto; Hiroaki Naraba; Hitonobu Tomoike; Naoharu Iwai
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Hypertension research : official journal of the Japanese Society of Hypertension     Volume:  27     ISSN:  0916-9636     ISO Abbreviation:  Hypertens. Res.     Publication Date:  2004 May 
Date Detail:
Created Date:  2004-06-16     Completed Date:  2004-07-15     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  9307690     Medline TA:  Hypertens Res     Country:  Japan    
Other Details:
Languages:  eng     Pagination:  327-31     Citation Subset:  IM    
Affiliation:
National Cardiovascular Center, Suita, Japan.
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MeSH Terms
Descriptor/Qualifier:
Adult
Aged
Aged, 80 and over
Asian Continental Ancestry Group / genetics*,  statistics & numerical data
Blood Pressure
Carrier Proteins / genetics*
Gene Frequency
Genes, Recessive*
Genotype
Heterozygote
Humans
Hydrogen-Ion Concentration
Japan / epidemiology
Kidney Diseases / epidemiology,  genetics*,  physiopathology,  urine
Kidney Tubules*
Middle Aged
Mutation*
Prevalence
Receptors, Drug / genetics*
Sodium Chloride Symporters
Symporters*
Urine / chemistry
Chemical
Reg. No./Substance:
0/Carrier Proteins; 0/Receptors, Drug; 0/SLC12A3 protein, human; 0/Sodium Chloride Symporters; 0/Symporters; 0/thiazide receptor

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