Background: Hypertensive patients have a younger trend, and studies on the role of genetic factors in hypertension susceptibility have been inconsistent. Aldehyde dehydrogenases 2 (ALDH2) and apolipoprotein E (APOE) are involved in the pathophysiological processes of hypertension. To investigate the relationship of and polymorphisms with hypertension in middle-aged (30-59 years old) and elderly (≥60 years old) persons.
Methods: Two thousand six hundred and ten hypertensive patients and 1921 controls were included (between 30 and 100 years old). The genotypes of common polymorphisms in and genes ( rs429358, rs7412, and rs671) of the subjects were analyzed by polymerase-chain reaction (PCR)-microarray. Statistical analyses (Student's -test, Mann-Whitney -test, test, and logistic regression analysis) were performed with SPSS v21.0.
Results: There were 4531 participants (66.60 ± 12.10 years old) in this study, including 3057 (67.5%) males and 1474 (32.5%) females. There were no significant differences in distributions of 2 rs671, rs429358/rs7412 genotypes and alleles between hypertensive patients and controls. Persons with rs671 G/A or A/A genotype were less likely to have hypertension (G/A+A/A vs G/G: gender-, age-, smoking-, and drinking-adjusted OR 0.885, 95% CI 0.785-0.997, =0.045), while rs671 A/A+ rs429358 or rs7412 wild-type genotype may decrease the risk of hypertension. In middle-aged group, rs671 G/A+ rs429358 T/C carriers (adjusted OR 0.547, 95% CI 0.350-0.856, =0.008), and rs671 A/A+ rs7412 C/C genotypes (adjusted OR 0.567, 95% CI 0.361-0.891, =0.014) were less likely to have hypertension. In elderly group, rs7412 T/T carriers were more likely to have hypertension (rs671 T/T vs C/C: adjusted OR 4.755, 95% CI 1.075-21.027, =0.040; rs671 T/T vs C/C or C/T: adjusted OR 4.734, 95% CI 1.071-20.928, =0.040).
Conclusion: Polymorphism-polymorphism interactions of rs671 and rs429358/rs7412 may effect on hypertension susceptibility. Different genotypes comparison shows different roles in middle-aged and elderly people, respectively.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10017832 | PMC |
http://dx.doi.org/10.2147/IJGM.S402437 | DOI Listing |
PLoS One
January 2025
Division of Life Science, Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong, China.
Coronary artery disease (CAD) is a multigenic condition influenced by both nature and nurture (60% to 40%). Prognosis of CAD is based on familial patterns. This study examined and analyzed the susceptibility of CAD to genetic variants in various Pakistani families.
View Article and Find Full Text PDFSci Rep
December 2024
Dipartimento di Medicina, Chirurgia e Farmacia, University of Sassari, Viale San Pietro 43, Sassari, 07100, Italy.
More than two decades ago, in the central-eastern region of the Mediterranean island of Sardinia, a mountain area was identified where the population displays exceptional longevity, especially among men (the Longevity Blue Zone, LBZ). This community was thoroughly investigated to understand the underlying causes of the phenomenon. The present study analyzed 11 genetic markers previously associated with increased survival in several long-lived populations.
View Article and Find Full Text PDFJ Psychopharmacol
December 2024
Faculty of Sport, Allied Health and Performance Science, St Mary's University Twickenham, London, UK.
Background: Research on caffeine and cognitive performance remains controversial. Variations in genes associated with caffeine metabolism and response such as and may account for variable findings.
Aim: To investigate caffeine × gene interactions on cognitive performance in all key domains of cognition in healthy individuals.
Clin Chim Acta
January 2025
Department of Molecular Biology, National AIDS Research Institute Pune 411026, India. Electronic address:
Basic Clin Neurosci
January 2024
Pathology and Stem Cell Research Center, Faculty of Medicine, Kerman University of Medical Sciences, Kerman, Iran.
Introduction: The apolipoprotein E () genotype has a heterogeneous distribution throughout the world. The present study aimed to characterize the genotype (, ) in healthy individuals compared with Alzheimer cases in Kerman, southeastern Iran, by two standard mutation scanning methods.
Methods: In this case-control study, 90 Alzheimer patients as a case group and 90 healthy individuals as a control group were examined.
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!