Role of Raptor Gene Variants in Hypertension: Influence on Blood Pressure Independent of Salt Intake in White Population

• Published in: Hypertension (Dallas, Tex. 1979) Vol. 81; no. 5; pp. 1167 - 1177
• Main Authors: Aljaibeji, Hayat, Heydarpour, Mahyar, Stanton, Ana Maria, Williams, Jonathan S, Pojoga, Luminita H, Romero, Jose R, Williams, Gordon H
• Format: Journal Article
• Language: English
• Published: United States 01-05-2024
• Subjects: Blood Pressure; Carrier Proteins - genetics; Female; Humans; Hypertension; Male; Mechanistic Target of Rapamycin Complex 1 - metabolism; Mechanistic Target of Rapamycin Complex 2 - metabolism; Nucleotides - metabolism; Rapamycin-Insensitive Companion of mTOR Protein - metabolism; Regulatory-Associated Protein of mTOR - genetics; Regulatory-Associated Protein of mTOR - metabolism; Sirolimus; Sodium Chloride, Dietary - metabolism; TOR Serine-Threonine Kinases - metabolism; White People; blood pressure; raptor; mTOR, rictor; hypertension; aldosterone; nucleotide
• ISSN: 0194-911X; 1524-4563
• DOI: 10.1161/HYPERTENSIONAHA.123.22273

The mTOR (mechanistic target of rapamycin) is an essential regulator of fundamental biological processes. mTOR forms 2 distinct complexes, mTORC1 (mTOR complex 1) when it binds with RAPTOR (Regulatory-associated Protein of mTOR) and mTORC2 (mTOR complex 2) when it associates with RICTOR (Rapamycin-insesitive companion of mTOR). Due to the previous link between the mTOR pathway, aldosterone, and blood pressure (BP), we anticipated that variants in the mTOR complex might be associated with salt-sensitive BP.
BP and other parameters were assessed after a one-week liberal Na
(200 mmol/d) and a one-week restricted Na
(10 mmol/d) diet in 608 White subjects from the Hypertensive Pathotype cohort, single-nucleotide variants in
,
, and
genes were obtained for candidate genes analyses.
The analysis revealed a significant association between a single nucleotide variants within the
gene and BP. Individuals carrying the
rs9901846 homozygous risk allele (AA) and heterozygous risk allele (GA) exhibited a 5 mm Hg increase in systolic BP on a liberal diet compared with nonrisk allele individuals (GG), but only in women. This single nucleotide variants effect was more pronounced on the restricted diet and present in both sexes, with AA carriers having a 9 mm Hg increase and GA carriers having a 5 mm Hg increase in systolic BP compared with GG. Interestingly, there were no significant associations between
or
gene variants and BP.
The
gene variation is associated with elevated BP in White participants, regardless of salt intake, specifically in females.