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Review
. 2024 Jan 27;12(1):19-26.
doi: 10.1159/000536505. eCollection 2024 Jan-Dec.

Genetic Variants Associated with Hypertension Risk: Progress and Implications

Affiliations
Review

Genetic Variants Associated with Hypertension Risk: Progress and Implications

David Curtis. Pulse (Basel). .

Abstract

Background: Genetic variants causing diseases with hypertension as a secondary feature have previously been identified. Studies focussing on primary hypertension have utilised common and latterly rare genetic variants in attempts to elucidate the genetic contribution to the risk of primary hypertension.

Summary: Using genome-wide association studies (GWASs), associations of hypertension with hundreds of common genetic variants have been reported, implicating thousands of genes. Individual variants have small effect sizes and cumulatively account for around 6% of genetic risk. The common variant signal is enriched for relevant tissues and physiological processes, while some variants are associated with traits expected to have secondary impacts on hypertension risk, such as fruit intake, BMI, or time watching television. Studies using rare variants obtained from exome sequence data have implicated a small number of genes for which impaired function has moderate effects on blood pressure and/or hypertension risk. Notably, genetic variants which impair elements of guanylate cyclase activation, stimulated by either natriuretic hormones or nitric oxide, increase hypertension risk. Conversely, variants impairing dopamine beta-hydroxylase or renin production are associated with lower blood pressure. Variants for which a definite effect can be designated remain cumulatively extremely rare and again make only a small contribution to overall genetic risk. Although these results are of interest, it is not clear that they provide radical new insights or identify drug targets which were not previously known. Nor does it seem that genetic testing could be useful in terms of quantifying disease risk or guiding treatment.

Key messages: Research has increased our knowledge about the relationship between naturally occurring genetic variation and risk of hypertension. Although some results serve to confirm our understanding of underlying physiology, their value in terms of potentially leading to practical advances in the management of hypertension appears questionable.

Keywords: ASXL1; DBH; DNMT3A; Exome; FES; GUCY1A1; GUCY1B1; GWAS; INPPL1; NPR1; REN; SMAD6.

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Conflict of interest statement

The author declares no conflict of interest.

Figures

Fig. 1.
Fig. 1.
Either membrane-bound or soluble guanylate cyclase can convert GTP to cGMP, producing smooth muscle relaxation and vasodilation, exerting a hypotensive effect. GUCY1A1 and GUCY1B1 code for subunits of a soluble guanylate cyclase responding to NO signalling. NPR1 codes for a membrane-bound guanylate cyclase responding to ANP, which is coded for by PPNA. Genetic variants damaging function of GUCY1A1, GUCY1B1, NPR1, or PPNA are associated with increased risk of hypertension, presumably through reduced guanylate cyclase activity.
Fig. 2.
Fig. 2.
Dopamine beta-hydroxylase converts dopamine to norepinephrine, which has a hypertensive effect. Genetic variants damaging function of DBH, which codes for dopamine beta-hydroxylase, are associated with reduced risk of hypertension, presumably through reduced production of norepinephrine.
Fig. 3.
Fig. 3.
In mice, Dnmt3a methylates Agtr1a, the gene which codes for angiotensin receptor type 1a (ATR). This methylation keeps Agtr1a expression under control, producing normal levels of ATR and a normal response to angiotensin (AT) with normal blood pressure. If Dnmt3a function is reduced then Agtr1a is hypomethylated, leading to abnormally increased expression and higher levels of ATR. The subsequent angiotensin receptor overactivity causes salt-sensitive hypertension. In humans, genetic variants damaging function of DNMT3A are associated with increased risk of hypertension, perhaps through a similar mechanism of loss of control of genes coding for angiotensin receptors.

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