Endothelial nitric oxide synthase gene polymorphisms associated with susceptibility to high altitude pulmonary edema in Chinese railway construction workers at Qinghai-Tibet over 4 500 meters above sea level.
- Author:
Sun YU-JING
1
;
Fang MING-WU
;
Niu WEN-QUAN
;
Li GUANG-PING
;
Liu JING-LIANG
;
Ding SHOU-QUAN
;
Xu YING
;
Yu GUO-SHU
;
Dong JIAN-QUN
;
Pan YUN-JUN
;
Dong WEI-YA
;
Wang TIAN
;
Cao JING-WEN
;
Li XIAO-BO
;
Wang ZHONG-XIANG
;
Yu GUANG-XUE
;
Sun HUI-CHENG
;
Jia ZHONG-HOU
;
Liu JUN
;
Wang XIAO-MING
;
Si QIN
;
Wu QI-XIA
;
Zhou WEN-YU
;
Zhu TONG-CHUN
;
Qiu CHANG-CHUN
Author Information
- Publication Type:Journal Article
- MeSH: Adolescent; Adult; Altitude; Base Sequence; Case-Control Studies; DNA Primers; Genotype; Haplotypes; Humans; Male; Middle Aged; Nitric Oxide; blood; Nitric Oxide Synthase Type III; genetics; Occupational Diseases; enzymology; genetics; Polymorphism, Genetic; Pulmonary Edema; enzymology; genetics; Tibet; Young Adult
- From: Chinese Medical Sciences Journal 2010;25(4):215-221
- CountryChina
- Language:English
-
Abstract:
OBJECTIVETo examine whether the polymorphisms of endothelial nitric oxide synthase (eNOS) gene are associated with the susceptibility to high altitude pulmonary edema (HAPE) in Chinese railway construction workers at Qinghai-Tibet where the altitude is over 4 500 m above sea level.
METHODSA case-control study was conducted including 149 HAPE patients in the construction workers and 160 healthy controls randomly recruited from their co-workers, matching the patients in ethnicity, age, sex, lifestyle, and working conditions. Three polymorphisms of eNOS gene, T-786C in promoter, 894G/T in exon 7, and 27bp variable number tandem repeat (VNTR) in intron 4, were genotyped using polymerase chain reaction (PCR) and confirmed with DNA sequencing.
RESULTSThe frequencies of 894T allele and heterozygous G/T of the 894G/T variant were significantly higher in HAPE patients group than in the control group (P=0.0028 and P=0.0047, respectively). However, the frequencies of the T-786C in promoter and the 27bp VNTR in intron 4 were not significantly different between the two groups. Haplotypic analysis revealed that the frequencies of two haplotypes (H3,T-T-b, b indicates 5 repeats of 27 bp VNTR; H6, C-G-a, a indicates 4 repeats of 27 bp VNTR) were significantly higher in HAPE patients (both Pü0.0001). On the contrary, the frequencies of H1 (T-G-b) and H2 (T-G-a) were lower in HAPE patients than in healthy controls (both Pü0.001).
CONCLUSIONSTwo haplotypes (T-T-b and C-G-a) may be strongly associated with susceptibility to HAPE. Compared with the individual alleles of eNOS gene, the interaction of multiple genetic markers within a haplotype may be a major determinant for the susceptibility to HAPE.