JOURNAL ARTICLE

Risk of preeclampsia in patients with maternal genetic predisposition to common medical conditions: a case-control study

Kathryn J Gray, Vesela P Kovacheva, Hooman Mirzakhani, Andrew C Bjonnes, Berta Almoguera, Melissa L Wilson, Sue Ann Ingles, Charles J Lockwood, Hakon Hakonarson, Thomas F McElrath, Jeffrey C Murray, Errol R Norwitz, S Ananth Karumanchi, Brian T Bateman, Brendan J Keating, Richa Saxena
BJOG: An International Journal of Obstetrics and Gynaecology 2020 August 2
32741103

OBJECTIVE: To assess whether women with a genetic predisposition to medical conditions known to increase preeclampsia risk have an increased risk of preeclampsia in pregnancy.

DESIGN: Case-control study.

SETTING AND POPULATION: Preeclampsia cases (n=498) and controls (n=1864) of European ancestry from 5 US sites genotyped on a cardiovascular gene-centric array.

METHODS: Significant single nucleotide polymorphisms (SNPs) from 21 traits in 7 disease categories (cardiovascular, inflammatory/autoimmune, insulin resistance, liver, obesity, renal, thrombophilia) with published genome-wide association studies (GWAS) were used to create a genetic instrument for each trait. Multivariable logistic regression was used to test the association of each continuous, scaled genetic instrument with preeclampsia. Odds of preeclampsia were compared across quartiles of the genetic instrument and evaluated for significance.

MAIN OUTCOME MEASURES: Genetic predisposition to medical conditions and their relationship with preeclampsia.

RESULTS: An increasing burden of risk alleles for elevated diastolic blood pressure (DBP) and increased body mass index (BMI) were associated with an increased risk of preeclampsia (DBP: overall OR 1.11 (95% CI: 1.01-1.21), p=0.025; BMI: OR 1.10 (1.00-1.20), p=0.042), while alleles associated with elevated alkaline phosphatase (ALP) were protective (OR 0.89 (0.82-0.97), p=0.008), driven primarily by pleiotropic effects of variants in the FADS gene region. The effect of DBP genetic loci was even greater in early-onset (<34 weeks) preeclampsia cases (OR 1.30 (1.08-1.56), p=0.005). For other traits, there was no evidence of an association.

CONCLUSIONS: These results suggest that the underlying genetic architecture of preeclampsia may be shared with other disorders, specifically hypertension and obesity.

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