Analysis of 200,000 Exome-Sequenced UK Biobank Subjects Implicates Genes Involved in Increased and Decreased Risk of Hypertension

David Curtis

PULSE · 2021-yil

Annotatsiya

Background: Previous analyses have identified common variants along with some specific genes and rare variants which are associated with risk of hypertension, but much remains to be discovered. Methods and Results: Exome-sequenced UK Biobank participants were phenotyped based on having a diagnosis of hypertension or taking anti-hypertensive medication to produce a sample of 66,123 cases and 134,504 controls. Variants with minor allele frequency (MAF) <0.01 were subjected to a gene-wise weighted burden analysis, with higher weights assigned to variants which are rarer and/or predicted to have more severe effects. Of 20,384 genes analysed, 2 genes were exome-wide significant, DNMT3A and FES. Also strongly implicated were GUCY1A1 and GUCY1B1, which code for the subunits of soluble guanylate cyclase. There was further support for the previously reported effects of variants in NPR1 and protective effects of variants in DBH. An inframe deletion in CACNA1D with MAF = 0.005, rs72556363, is associated with modestly increased risk of hypertension. Other biologically plausible genes highlighted consist of CSK, AGTR1, ZYX, and PREP. All variants implicated were rare, and cumulatively they are not predicted to make a large contribution to the population risk of hypertension. Conclusions: This approach confirms and clarifies previously reported findings and also offers novel insights into biological processes influencing hypertension risk, potentially facilitating the development of improved therapeutic interventions. This research has been conducted using the UK Biobank Resource.

Maqola ma’lumotlari
MualliflarDavid Curtis
JurnalPULSE
NashriyotPROFI университетининг
ISSN2074-1855, 2235-8668
Nashr sanasi2021-01-01
Jild9
Son1-2
Betlar17-29
TilIngliz
Ilmiy sohaPsixologiya
DOI10.1159/000517419
Indeksga qo‘shilgan2026-09-02

Ilmiy soha

Iqtibos keltirish

APADavid Curtis (2021). Analysis of 200,000 Exome-Sequenced UK Biobank Subjects Implicates Genes Involved in Increased and Decreased Risk of Hypertension. PULSE, 9(1-2), 17-29. https://doi.org/10.1159/000517419
GOST (OAK)David Curtis Analysis of 200,000 Exome-Sequenced UK Biobank Subjects Implicates Genes Involved in Increased and Decreased Risk of Hypertension // PULSE. – 2021. – T. 9, № 1-2. – P. 17-29. – DOI: 10.1159/000517419.
MLADavid Curtis. “Analysis of 200,000 Exome-Sequenced UK Biobank Subjects Implicates Genes Involved in Increased and Decreased Risk of Hypertension.” PULSE, 9(1-2), 17-29, 2021. https://doi.org/10.1159/000517419
ChicagoDavid Curtis. “Analysis of 200,000 Exome-Sequenced UK Biobank Subjects Implicates Genes Involved in Increased and Decreased Risk of Hypertension.” PULSE, 9(1-2), 17-29 (2021). https://doi.org/10.1159/000517419
HarvardDavid Curtis (2021) ‘Analysis of 200,000 Exome-Sequenced UK Biobank Subjects Implicates Genes Involved in Increased and Decreased Risk of Hypertension’, PULSE, 9(1-2), 17-29. https://doi.org/10.1159/000517419
BibTeX
@article{davidcurtis2021,
  title = {Analysis of 200,000 Exome-Sequenced UK Biobank Subjects Implicates Genes Involved in Increased and Decreased Risk of Hypertension},
  author = {David Curtis},
  journal = {PULSE},
  year = {2021},
  volume = {9},
  number = {1-2},
  pages = {17-29},
  doi = {10.1159/000517419},
  url = {https://doi.org/10.1159/000517419}
}

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