In:
Journal of Medical Genetics, BMJ, Vol. 55, No. 7 ( 2018-07), p. 459-468
Abstract:
Breast milk is the sole nutrition source during exclusive breastfeeding, and polyunsaturated fatty acids (FAs) are critical micronutrients in infant physical and cognitive development. There has been no prior genomewide association study of breast milk, hence our objective was to test for genetic association with breast milk FA composition. Methods We measured the fractional composition of 26 individual FAs in breast milk samples from three cohorts totalling 1142 Bangladeshi mothers whose infants were genotyped on the Illumina MEGA chip and replicated on a custom Affymetrix 30K SNP array (n=616). Maternal genotypes were imputed using IMPUTE. Results After running 33 separate FA fraction phenotypes, we found that SNPs known to be associated with serum FAs in the FADS1/2/3 region were also associated with breast milk FA composition (experiment-wise significance threshold 4.2×10 −9 ). Hypothesis-neutral comparison of the 33 fractions showed that the most significant genetic association at the FADS1/2/3 locus was with fraction of arachidonic acid (AA) at SNP rs174556, with a very large per major allele effect size of 17% higher breast milk AA level. There was no evidence of independent association at FADS1/2/3 with any other FA or SNP after conditioning on AA and rs174556. We also found novel significant experiment-wise SNP associations with: polyunsaturated fatty acid (PUFA) 6/PUFA3 ratio (sorting nexin 29 ), eicosenoic (intergenic) and capric (component of oligomeric Golgi complex 3) acids; and six additional loci at genomewide significance ( 〈 5×10 −8 ). Conclusions AA is the primary FA in breast milk influenced by genetic variation at the FADS1/2/3 locus, extending the potential phenotypes under genetic selection to include breast milk composition, thereby possibly affecting infant growth or cognition. Breast milk FA composition is influenced by maternal genetics in addition to diet and body composition.
Type of Medium:
Online Resource
ISSN:
0022-2593
,
1468-6244
DOI:
10.1136/jmedgenet-2017-105134
DOI:
10.1136/jmedgenet-2017-105134.supp1
DOI:
10.1136/jmedgenet-2017-105134.supp3
DOI:
10.1136/jmedgenet-2017-105134.supp4
DOI:
10.1136/jmedgenet-2017-105134.supp2
DOI:
10.1136/jmedgenet-2017-105134.supp5
DOI:
10.1136/jmedgenet-2017-105134.supp6
DOI:
10.1136/jmedgenet-2017-105134.supp7
DOI:
10.1136/jmedgenet-2017-105134.supp8
DOI:
10.1136/jmedgenet-2017-105134.supp9
DOI:
10.1136/jmedgenet-2017-105134.supp10
DOI:
10.1136/jmedgenet-2017-105134.supp11
Language:
English
Publisher:
BMJ
Publication Date:
2018
detail.hit.zdb_id:
2009590-9
SSG:
12
Bookmarklink