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. 2022 Mar 17;78:103948. doi: 10.1016/j.ebiom.2022.103948

Table 1.

Mendelian randomization results of causal risk proteins on childhood neurodevelopmental disorders.a,b

Method No. of SNPs MR analysis
Heterogeneity test
MR-Egger intercept P
OR (95%) P Cochran's Q I2 P
MAPKAPK3 on ASD
 IVW 20 1.09(1.05,1.13) 1.43e-06 15.2 0% 0.710 -
 MR-Egger 20 1.10(1.03,1.18) 7.61e-03 15.2 0% 0.711 0.843
 Weighted median 20 1.09(1.04,1.15) 3.03e-04 - - - -
MRPL33 on. ASD
 IVW 23 1.07(1.04,1.11) 5.37e-06 16.3 0% 0.800
 MR-Egger 23 1.12(1.07,1.17) 5.63e-07 12.8 0% 0.939 0.011
 Weighted median 23 1.08(1.03,1.13) 8.33e-04 - - -
MANBA on ADHD
 IVW 14 0.91(0.88,0.95) 8.97e-06 15.1 13.6% 0.304 -
 MR-Egger 14 0.86(0.81,0.93) 3.68e-05 11.2 0% 0.596 0.072
 Weighted median 14 0.89(0.85,0.94) 3.65e-06 - - - -

Abbreviations: MR, Mendelian Randomization; ASD, autism spectrum disorder; ADHD, attention-deficit hyperactivity disorder.

a

Results from 2-sample MR analysis; main analysis method: outliers identified and removed by MR PRESSO tool; estimated associations reported as OR of outcome per unit increase in log odds of the quantification of specific protein.

b

Genetic instruments selected from GWAS of plasma proteome, selection threshold P less than 1 × 10−5, pruned at linkage disequilibrium R2 less than .001 (10 megabytes pair window); No. of SNPs refers to the number of genetic instruments included in final MR analysis.