Table 5 Results of regressing offspring cardiometabolic risk factors on paternal GRSa after conditioning on offspring GRSa in father–offspring pairs.

From: Mendelian randomization study of maternal influences on birthweight and future cardiometabolic risk in the HUNT cohort

 

Autosomal SNPs (N = 204)

Autosomal SNPs with maternal effect (N = 71)

Autosomal SNPs with maternal effect only (N = 31)

Outcome

Effect estimate

SE

p-value

Effect estimate

SE

p-value

Effect estimate

SE

p-value

SBP (mmHg)

−0.0088

0.0077

0.2512

−0.0008

0.0076

0.9143

0.0097

0.0076

0.2050

DBP (mmHg)

−0.0048

0.0075

0.5238

0.0061

0.0074

0.4114

0.0025

0.0075

0.7412

Glucose (mmol/L)b

0.0031

0.0081

0.6102

0.0086

0.0080

0.2786

0.0017

0.0075

0.8362

Total cholesterol (mmol/L)

−0.0027

0.0079

0.7318

−0.0085

0.0078

0.2798

−0.0102

0.0079

0.1951

LDL cholesterol (mmol/L)

−0.0009

0.0075

0.9445

−0.0019

0.0074

0.8027

−0.0033

0.0075

0.6637

HDL cholesterol (mmol/L)

−0.0011

0.0079

0.8912

−0.0046

0.0078

0.5494

−0.0131

0.0077

0.0959

Triglycerides (mmol/L)b

−1.2 × 10−03

0.0080

0.8851

−0.0039

0.0079

0.6087

−0.0039

0.0079

0.6238

BMIb

−0.0016

0.0082

0.6710

−0.0001

0.0068

1

0.0119

0.0080

0.1414

  1. The regression coefficients give the estimated expected change in offspring cardiometabolic outcome (in the units listed in column 1) per one unit (i.e. allele) increase in paternal genetic risk score after conditioning on offspring genetic risk score. Effect estimates and standard errors are standardized. P-values reflect minus two log-likelihood chi-square tests between the full model and a sub-model where the relevant parameter is fixed to zero. All p-values are two sided uncorrected for multiple testing. All analyses are adjusted for age, sex, measurement occasion and GRS of offspring.
  2. GRS genetic risk score, SBP systolic blood pressure, DBP diastolic blood pressure, Glucose non-fasting glucose, BMI body mass index, LDL non-fasting low density lipoprotein, HDL non-fasting high density lipoprotein, mmol/L millimol per litre, SNP single nucleotide polymorphism, N number of individuals, SE standard error.
  3. aPaternal and offspring GRS were coded so that increasing dosages reflected maternal alleles associated with increased offspring birthweight based on conditional GWAS results previously published.
  4. bOffspring phenotype first (natural) logarithm transformed.