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dc.contributor.authorMunthali, Richard J
dc.contributor.authorSahibdeen, Venesa
dc.contributor.authorKagura, Juliana
dc.contributor.authorHendry, Liesl M
dc.contributor.authorNorris, Shane A
dc.contributor.authorOng, Ken K
dc.contributor.authorDay, Felix R
dc.contributor.authorLombard, Zané
dc.date.accessioned2018-08-02T06:05:21Z
dc.date.available2018-08-02T06:05:21Z
dc.date.issued2018-08-01
dc.identifier.citationGenes & Nutrition. 2018 Aug 01;13(1):24
dc.identifier.urihttps://www.repository.cam.ac.uk/handle/1810/278606
dc.description.abstractAbstract Background Ninety-seven independent single nucleotide polymorphisms (SNPs) are robustly associated with adult body mass index (BMI kg/m2) in Caucasian populations. The relevance of such variants in African populations at different stages of the life course (such as childhood) is unclear. We tested whether a genetic risk score composed of the aforementioned SNPs was associated with BMI from infancy to early adulthood. We further tested whether this genetic effect was mediated by conditional weight gain at different growth periods. We used data from the Birth to Twenty Plus Cohort (Bt20+), for 971 urban South African black children from birth to 18 years. DNA was collected at 13 years old and was genotyped using the Metabochip (Illumina) array. The weighted genetic risk score (wGRS) for BMI was constructed based on 71 of the 97 previously reported SNPs. Results The cross-sectional association between the wGRS and BMI strengthened with age from 5 to 18 years. The significant associations were observed from 11 to 18 years, and peak effect sizes were observed at 13 and 14 years of age. Results from the linear mixed effects models showed significant interactions between the wGRS and age on longitudinal BMI but no such interactions were observed in sex and the wGRS. A higher wGRS was associated with an increased relative risk of belonging to the early onset obese longitudinal BMI trajectory (relative risk = 1.88; 95%CI 1.28 to 2.76) compared to belonging to a normal longitudinal BMI trajectory. Adolescent conditional relative weight gain had a suggestive mediation effect of 56% on the association between wGRS and obesity risk at 18 years. Conclusions The results suggest that genetic susceptibility to higher adult BMI can be tracked from childhood in this African population. This supports the notion that prevention of adult obesity should begin early in life. The genetic risk score combined with other non-genetic risk factors, such as BMI trajectory membership in our case, has the potential to be used to screen for early identification of individuals at increased risk of obesity and other related NCD risk factors in order to reduce the adverse health risk outcomes later.
dc.titleGenetic risk score for adult body mass index associations with childhood and adolescent weight gain in an African population
dc.typeJournal Article
dc.date.updated2018-08-02T06:05:18Z
dc.language.rfc3066en
dc.rights.holderThe Author(s)
dc.identifier.doi10.17863/CAM.25947
rioxxterms.versionofrecord10.1186/s12263-018-0613-7


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