CYP17A1 Enzyme Activity Is Linked to Ambulatory Blood Pressure in a Family-Based Population Study

BACKGROUND Genome-wide association studies have linked CYP17A1 coding for the steroid hormone synthesizing enzyme 17α-hydroxylase (CYP17A1) to blood pressure (BP). We hypothesized that the genetic signal may translate into a correlation of ambulatory BP (ABP) with apparent CYP17A1 activity in a fami...

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Veröffentlicht in:American journal of hypertension 2016-04, Vol.29 (4), p.484-493
Hauptverfasser: Ackermann, Daniel, Pruijm, Menno, Ponte, Belen, Guessous, Idris, Ehret, Georg, Escher, Geneviève, Dick, Bernhard, Al-Alwan, Heba, Vuistiner, Philippe, Paccaud, Fred, Burnier, Michel, Péchère-Bertschi, Antoinette, Martin, Pierre-Yves, Vogt, Bruno, Mohaupt, Markus, Bochud, Murielle
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Sprache:eng
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Zusammenfassung:BACKGROUND Genome-wide association studies have linked CYP17A1 coding for the steroid hormone synthesizing enzyme 17α-hydroxylase (CYP17A1) to blood pressure (BP). We hypothesized that the genetic signal may translate into a correlation of ambulatory BP (ABP) with apparent CYP17A1 activity in a family-based population study and estimated the heritability of CYP17A1 activity. METHODS In the Swiss Kidney Project on Genes in Hypertension, day and night urinary excretions of steroid hormone metabolites were measured in 518 participants (220 men, 298 women), randomly selected from the general population. CYP17A1 activity was assessed by 2 ratios of urinary steroid metabolites: one estimating the combined 17α-hydroxylase/17,20-lyase activity (ratio 1) and the other predominantly 17α-hydroxylase activity (ratio 2). A mixed linear model was used to investigate the association of ABP with log-transformed CYP17A1 activities exploring effect modification by urinary sodium excretion. RESULTS Daytime ABP was positively associated with ratio 1 under conditions of high, but not low urinary sodium excretion (P interaction
ISSN:0895-7061
1941-7225
DOI:10.1093/ajh/hpv138