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Aim We aimed to investigate the association between single nucleotide polymorphisms (SNPs) in the angiotensin-converting enzyme (ACE) gene and hypertension in elderly Japanese individuals. Methods This cross-sectional validation study was nested within the Nagasaki Islands Study (NaIS), involving 1,766 community-dwelling participants aged 65 years and older. Height and weight were measured. Body mass index (BMI) was calculated from height and weight, and blood pressure was measured by trained staff. Antihypertensive medication use and lifestyle factors, including alcohol consumption, smoking habits, and exercise, were assessed by interviews. The SNP (rs4309) was genotyped using fluorescent hydrolysis probes from peripheral blood mononuclear cells. Hypertension was defined as using antihypertensive medication or a systolic blood pressure of ≥140 mmHg and/or a diastolic blood pressure of ≥90 mmHg in those not on medication. Logistic regression analysis was used to calculate adjusted odds ratios (ORs) for hypertension, adjusting for potential confounders. Results Hypertension prevalence was higher in the CC/CT genotype group compared to the TT group (71.5% vs 66.4%, p=0.025). Logistic regression showed that the CC/CT genotype was independently associated with a higher likelihood of hypertension than the TT genotype (OR=1.25, 95% confidence interval (CI) 1.001-1.548) after adjusting for age, BMI, gender, alcohol consumption, smoking, and exercise. Conclusion The CC and CT genotypes of the ACE gene were independently associated with hypertension, regardless of age, BMI, gender, and lifestyle factors. These findings support a genetically informed approach to hypertension prevention.
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http://dx.doi.org/10.7759/cureus.82193 | DOI Listing |
Biol Res
September 2025
Department of Biochemistry and Systems Biology, School of Biosciences, College of Natural Sciences, Makerere University, P.O. Box 7062, Kampala, Uganda.
Background: Sickle cell disease (SCD) is characterised by chronic oxidative stress. However, there is limited information on how polymorphisms in cytokine genes influence oxidative stress in SCD patients. The study aimed to determine the effect of Interleukin gene (IL-10) and Tumor Necrosis Factor (TNF) polymorphisms on oxidative stress and cytokine levels in SCD patients from Mulago hospital.
View Article and Find Full Text PDFbioRxiv
August 2025
Department of Medicine, University of Rochester Medical Center, Rochester, NY, 14642, USA.
The hypothalamic paraventricular nucleus (PVN) integrates neuroendocrine and autonomic signals that regulate blood pressure and metabolism. Although the renin-angiotensin system (RAS) is implicated in neurogenic hypertension and obesity, cell-type-specific expression and regulation of its components within the PVN remain poorly understood. Here, we employed single-nucleus RNA sequencing (snRNA-seq) to profile the transcriptomic landscape of the PVN in male mice under baseline conditions and in models of DOCA-salt-induced hypertension and high-fat diet (HFD)-induced obesity.
View Article and Find Full Text PDFBMC Nephrol
September 2025
Division of Nephrology, Hypertension, and Kidney Transplantation, Department of Medicine, University of California, Irvine, 3800 Chapman Ave, Suite 6200, Orange, CA, 92868-3298, USA.
Background: Denys-Drash syndrome (DDS) is defined by early onset nephrotic syndrome rapidly progressing to end stage renal disease (ESRD) before 4 years of age, male pseudohermaphroditism, and Wilms tumor (WT). DDS is associated with mutations in the gene, most commonly in exons 8 or 9. mutations are associated with nephrotic syndrome and renal dysfunction, with an onset in early adulthood.
View Article and Find Full Text PDFNat Protoc
September 2025
The African Center of Excellence in Bioinformatics and Data Intensive Sciences, Makerere University, Kampala, Uganda.
Tandem repeats (TRs) are highly variable loci in the human genome that are linked to various human phenotypes. Accurate and reliable genotyping of TRs is important in understanding population TR variation dynamics and their effects in TR-trait association studies. In this protocol, we describe how to generate high-quality consensus TR genotypes for population genomics studies.
View Article and Find Full Text PDFSci Rep
August 2025
West African Centre for Cell Biology of Infectious Pathogens (WACCBIP), College of Basic and Applied Sciences, University of Ghana, Legon, Accra, Ghana.
Triple-negative breast cancer (TNBC) is challenging to treat due to its aggressive nature. Its lack of hormone receptors renders conventional therapies less effective. This study assessed the efficacy of a novel compound, compound 2, in modulating TNBC cell behaviour.
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