Key result
Common NOS1AP genetic variation linked to ~26% greater risk of sudden cardiac death.
Why the study?
Common variation within the NOS1AP locus is strongly related to QT interval, a risk factor for sudden cardiac death, but additional evidence for association with SCD was needed.
Is genetic variation in the NOS1AP locus associated with sudden cardiac death in older adults of European ancestry?
Cohort (n=5,974)
Yes
Is genetic variation in the NOS1AP locus associated with sudden cardiac death in older adults of European ancestry?
Hazard Ratio: 1.26
p-value: p=0.0011
Common genetic variation in the NOS1AP locus is associated with an increased risk of sudden cardiac death in populations of European ancestry.
Should not yet change SCD prevention; extends candidate-gene associations but requires prospective validation before risk-stratification use.
Common variation within the nitric oxide-1 synthase activator protein (NOS1AP) locus is strongly related to QT interval, a sudden cardiac death (SCD) risk factor. A recent report describes common variation in NOS1AP associated with SCD in a US population of European ancestry. The objective of the current study was to obtain additional evidence by investigating the association between NOS1AP variants and SCD in the prospective population-based Rotterdam Study. The study population consisted of 5974 European ancestry subjects, aged 55 years and older, genotyped on Illumina arrays. SCD was defined according to European Society of Cardiology guidelines. Smoking, body mass index, diabetes mellitus, hypertension, heart failure and myocardial infarction were used as covariates in Cox proportional hazard models. Results were combined with reported evidence using inverse-variance weighted meta-analysis. Two hundred and eight (109 witnessed) cases of SCD occurred during a mean follow-up of 10.4 years. Within the Rotterdam Study alone, no significant associations were observed. Upon pooling of results with existing data, we observed strengthening of existing evidence for rs16847549 (US data HR = 1.31, P = 0.0024; Rotterdam Study HR = 1.18, P = 0.16; joint HR = 1.26, P = 0.0011). When the case definition in the Rotterdam Study was restricted to witnessed SCD, association of rs16847549 with SCD became stronger (joint P = 0.00019) and additionally the association between rs12567209 and SCD gained significance (US data HR = 0.57, P = 0.0035; Rotterdam Study HR = 0.69, P = 0.23; joint HR = 0.60, P = 0.0018). In conclusion, this study provided additional evidence for association between genetic variation within NOS1AP and SCD. The mechanism by which this effect is exerted remains to be elucidated.
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Eijgelsheim et al. (2009) conducted a cohort in Sudden cardiac death (n=5,974). NOS1AP genetic variants (rs16847549) vs. Reference genotype was evaluated on Sudden cardiac death (HR 1.26, p=0.0011). Common genetic variation in the NOS1AP locus (rs16847549) was significantly associated with an increased risk of sudden cardiac death across pooled US and Rotterdam cohorts (joint HR 1.26, P=0.0011).
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