rs11191454 - AS3MT, BORCS7-ASMT
Magnitude 2.2 · 2 studies on file
Reported associations
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Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis - Unknown journal (n.d.) · Unknown authors · PubMed 23453885
ABSTRACT: Summary Background Findings from family and twin studies suggest that genetic contributions to psychiatric disorders do not in all cases map to present diagnostic categories. We aimed to identify specific variants underlying genetic effects shared between the five disorders in the Psychiatric Genomics Consortium: autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia. Methods We analysed genome-wide single-nucleotide polymorphism (SNP) data for the five disorders in 33 332 cases and 27 888 controls of European ancestory. To characterise allelic effects on each disorder, we applied a multinomial logistic regression procedure with model selection to identify the best-fitting model of relations between genot
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Causal relevance of different blood pressure traits on risk of cardiovascular diseases: GWAS and Mendelian randomisation in 100,000 Chinese adults - Unknown journal (n.d.) · Unknown authors · PubMed 39048560
ABSTRACT: Elevated blood pressure (BP) is major risk factor for cardiovascular diseases (CVD). Genome-wide association studies (GWAS) conducted predominantly in populations of European ancestry have identified >2,000 BP-associated loci, but other ancestries have been less well-studied. We conducted GWAS of systolic, diastolic, pulse, and mean arterial BP in 100,453 Chinese adults. We identified 128 non-overlapping loci associated with one or more BP traits, including 74 newly-reported associations. Despite strong genetic correlations between populations, we identified appreciably higher heritability and larger variant effect sizes in Chinese compared with European or Japanese ancestry populations. Using instruments derived from these GWAS, multivariable Mendelian randomisation demonstrated
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Lifestyle context
Concrete actions anchored to the cited research. We do not prescribe, we describe.
Bloodwork
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Diastolic blood pressure monitoring High
rs11191454-A allele is strongly associated with elevated diastolic blood pressure (effect 0.812 mmHg per allele, p=3.00e-43)
Annual blood pressure measurement starting in early adulthood; baseline by age 20-25
Discuss with your doctor
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Psychiatric screening for genetic risk Moderate
rs11191454-A allele associated with increased risk for autism, ADHD, bipolar disorder, depression, and schizophrenia (OR=1.13, p=1.39e-8)
Discuss baseline mental health assessment and ongoing screening with healthcare provider
Lifestyle
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Cardiovascular risk reduction High
A allele carriers have elevated diastolic BP risk, modifiable through evidence-based interventions
Aerobic exercise 150 min/week, DASH diet daily, sodium <2300 mg/day, stress reduction daily