scholarly journals Genetic variants of endothelial PAS domain protein 1 are associated with susceptibility to acute mountain sickness in individuals unaccustomed to high altitude: A nested case-control study

2015 ◽  
Vol 10 (3) ◽  
pp. 907-914 ◽  
Author(s):  
LI GUO ◽  
JIHANG ZHANG ◽  
JUN JIN ◽  
XUBIN GAO ◽  
JIE YU ◽  
...  
2019 ◽  
Vol 41 (12) ◽  
pp. 1090-1096
Author(s):  
Yao Zhu ◽  
Shu-Chang Hu ◽  
Pei-Wen Zheng ◽  
Ming-Juan Jin ◽  
Meng-Ling Tang ◽  
...  

2020 ◽  
Vol 2020 ◽  
pp. 1-13
Author(s):  
Jingbin Ke ◽  
Chuan Liu ◽  
Shiyong Yu ◽  
Shizhu Bian ◽  
Chen Zhang ◽  
...  

Background. The aims of this study were to explore the characteristics of left ventricular (LV) functional changes in subjects with or without acute mountain sickness (AMS) and their associations with AMS incidence. Methods. A total of 589 healthy men were enrolled and took a trip from Chengdu (500 m, above sea level (asl)) to Lhasa (3700 m, asl) by airplane. Basic characteristics, physiological data, and echocardiographic parameters were collected both at Chengdu and Lhasa, respectively. AMS was identified by the Lake Louise Questionnaire Score. Results. The oxygen saturation (SpO2), end-systolic volume index, end-diastolic volume index (EDVi), stroke volume index (SVi), E-wave velocity, and E/A ratio were decreased, whereas the heart rate (HR), ejection fraction, cardiac index (CI), and A-wave velocity were increased at the third day after arrival, as evaluated by an oximeter and echocardiography. However, AMS patients showed higher HR and lower EDVi, SVi, CI, E-wave velocity, and E/A ratio than AMS-free subjects. Among them, SVi, which is mainly correlated with the changes of EDVi and altered LV filling pattern, was the most valuable factor associated with AMS incidence following receiver-operator characteristic curves and linear and Poisson regression. Compared with subjects in the highest SVi tertile, subjects in the middle SVi tertile showed higher multivariable Incidence Rate Ratios (IRR) for AMS with higher incidences of mild headache and gastrointestinal symptoms, whereas subjects in the lowest SVi tertile showed even higher multivariable IRR with higher incidences of all the symptoms. Conclusions. This relatively large-scale case-control study revealed that the reduction of SVi correlated with the altered LV filling pattern was associated with the incidence and clinical severity of AMS.


DNA Repair ◽  
2015 ◽  
Vol 28 ◽  
pp. 21-27 ◽  
Author(s):  
Tonje Skarpengland ◽  
Lars Erik Laugsand ◽  
Imre Janszky ◽  
Luisa Luna ◽  
Bente Halvorsen ◽  
...  

2020 ◽  
Vol 20 (2) ◽  
pp. 735-744
Author(s):  
Houssam Boulenouar ◽  
Sarah Aicha Lardjam Hetraf ◽  
Hadjira Ouhaibi Djellouli ◽  
Djabaria Naima Meroufel ◽  
Faouzia Zemani Fodil ◽  
...  

Background: Coronary Heart Disease (CHD) is a major cause of morbidity and mortality over the world; intermediate traits associated with CHD commonly studied can be influenced by a combination of genetic and environmental factors. Objective: We found previously significant association between three genetic polymorphisms, and the lipid profile variations in the Algerian population. Considering these findings, we therefore decided to assess the relationships between these polymorphisms and CHD risk. Methods: We performed a population-based, cross-sectional study, of 787 individuals recruited in the city of Oran, in which, a nested case-control study for MetS, T2D, HBP, obesity and CHD were performed. Subjects were genotyped for four SNP rs7412, rs429358 rs4420638 and rs439401 located in the 19q13.32 region. Results: The T allele of rs439401 confers a high risk of hypertension with an odds ratio (OR) of 1.46 (95% CI [1.12-1.9], p = 0.006) and the G allele of rs4420638 was significantly associated with a decreased risk of obesity, OR 0.48 (95% CI [0.29- 0.81], p = 0.004). No associations were found for MetS, T2D and CHD. Conclusion: Although the studied genetic variants were not associated with the risk of CHD, the 19q13.32 locus was associated with some of the cardiometabolic disorders in Algerian subjects. Keywords: Genetics; high blood pressure; CHD risk; obesity; Algerian population.


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