Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 Jun 4:16:1608423.
doi: 10.3389/fgene.2025.1608423. eCollection 2025.

NOS3 rs3918188C>A is associated with susceptibility to resistant hypertension while CES1 genetic variation was not associated with resistant hypertension among South Africans

Jonathan N Katsukunya  1   2 , Revina Naicker  1   2 , Nyarai D Soko  1   2   3 , Dirk Blom  2   4 , Phumla Sinxadi  2   5 , Emile R Chimusa  6 , Brian Rayner  2   7 , Erika Jones  2   7 , Collet Dandara  1   2
Affiliations

NOS3 rs3918188C>A is associated with susceptibility to resistant hypertension while CES1 genetic variation was not associated with resistant hypertension among South Africans

Jonathan N Katsukunya et al. Front Genet. .

Abstract

Introduction: Genetic variation in genes coding for enzymes metabolising antihypertensive drugs, may affect the efficacy of angiotensin converting enzyme (ACE) inhibitors such as enalapril, potentially leading to resistant hypertension (RHTN). We set out to evaluate the contribution of genetic variation in CES1 and NOS3 genes on susceptibility to RHTN, as well as estimate the frequencies of CES1 copy number variation (CNV) in African and Mixed Ancestry (MA) populations of South Africa.

Methods: Using a retrospective age, sex and ethnicity matched case-control study design, 379 participants with hypertension belonging to the African and MA ethnic groups were recruited. Cases were participants with RHTN (i.e., blood pressure (BP) ≥140/90 mmHg on ≥3 antihypertensive drugs or BP < 140/90 mmHg on >3 antihypertensive drugs, including a diuretic). Cases were matched to controls with similar characteristics (age (±5 years), sex and ethnicity) in a 1:1 ratio. Controls were participants with hypertension that was under control (BP < 140/90 mmHg on ≤3 antihypertensive drugs). Five polymorphisms in CES1 and NOS3 were characterized using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP), quantitative PCR and validated using Sanger sequencing. The additive model of inheritance and multivariable logistic regression were used to determine associations between genotypes and RHTN while adjusting for potential confounding variables.

Results and discussion: NOS3 rs3918188A/A (aOR: 0.13; CI: 0.04-0.41; P = 0.0009) genotype and NOS3 rs2070744-rs1798883-rs3918188G-T-A haplotype (OR: 0.54; CI: 0.37-0.78; P = 0.001) appeared to confer protection against RHTN among MA participants only. CES1 rs2244613C>A and CES1 CNV were not significantly associated with RHTN. However, there appeared to be quantitative differences in CES1 CNV profiles across ethnic groups. We speculate that NOS3 rs3918188A allele may affect NOS3 gene expression, potentially leading to increased amounts of the vasodilator, nitric oxide (NO) and favourable outcomes in individuals taking antihypertensives drugs such as enalapril.

Conclusion: NOS3 genetic variation seems important in the susceptibility to RHTN among Africans and requires further studies.

Keywords: ACE inhibitors; Africans; CES1; NOS3; enalapril; hypertension; pharmacogenomics.

PubMed Disclaimer

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.

Figures

FIGURE 1
FIGURE 1
Linkage disequilibrium (LD) plots (D’) for African and Mixed Ancestry participants for NOS3 rs1799983G>T, rs2070744C>T and rs3918188C>A SNPs.
See this image and copyright information in PMC

Similar articles

See all similar articles

References

    1. Acelajado M. C., Pisoni R., Dudenbostel T., Dell'Italia L. J., Cartmill F., Zhang B., et al. (2012). Refractory hypertension: definition, prevalence, and patient characteristics. J. Clin. Hypertens. (Greenwich) 14 (1), 7–12. 10.1111/j.1751-7176.2011.00556.x - DOI - PMC - PubMed
    1. Amrani A., Baba Hamed M. B., Mesli Talebbendiab F. (2015). Association study between some renin-angiotensin system gene variants and essential hypertension in a sample of Algerian population: case control study. Ann. Biol. Clin. Paris. 73 (5), 557–563. 10.1684/abc.2015.1069 - DOI - PubMed
    1. Amrani-Midoun A., Kiando S. R., Treard C., Jeunemaitre X., Bouatia-Naji N. (2019). Genetic association study between T-786C NOS3 polymorphism and essential hypertension in an Algerian population of the Oran city. Diabetes Metab. Syndr. 13 (2), 1317–1320. 10.1016/j.dsx.2019.02.024 - DOI - PubMed
    1. Baysoy A., Tian X., Zhang F., Renauer P., Bai Z., Shi H., et al. (2024). Spatially resolved in vivo CRISPR screen sequencing via perturb-DBiT. bioRxiv. 10.1101/2024.11.18.624106 - DOI
    1. Boberg M., Vrana M., Mehrotra A., Pearce R. E., Gaedigk A., Bhatt D. K., et al. (2017). Age-dependent absolute abundance of hepatic carboxylesterases (CES1 and CES2) by LC-MS/MS proteomics: application to PBPK modeling of oseltamivir in vivo pharmacokinetics in infants. Drug Metab. Dispos. 45 (2), 216–223. 10.1124/dmd.116.072652 - DOI - PMC - PubMed

LinkOut - more resources