rs10889551 - LEPR
Magnitude 2.2 · 1 study on file
Reported associations
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Characterization of the genetic architecture of infant and early childhood body mass index. - Nature metabolism (2022) · Helgeland Ø, Vaudel M, Sole-Navais P, Flatley C, Juodakis J, Bacelis J, Koløen IL, Knudsen GP, Johansson BB, Magnus P, Kjennerud TR, Juliusson PB, Stoltenberg C, Holmen OL, Andreassen OA, Jacobsson B, Njølstad PR, Johansson S · PubMed 35315439
Early childhood obesity is a growing global concern; however, the role of common genetic variation on infant and child weight development is unclear. Here, we identify 46 loci associated with early childhood body mass index at specific ages, matching different child growth phases, and representing four major trajectory patterns. We perform genome-wide association studies across 12 time points from birth to 8 years in 28,681 children and their parents (27,088 mothers and 26,239 fathers) in the Norwegian Mother, Father and Child Cohort Study. Monogenic obesity genes are overrepresented near identified loci, and several complex association signals near LEPR, GLP1R, PCSK1 and KLF14 point towards a major influence for common variation affecting the leptin-melanocortin system in early life, prov
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Lifestyle context
Concrete actions anchored to the cited research. We do not prescribe, we describe.
Screening
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weight gain and BMI trend from early childhood Moderate
rs10889551-A allele genome-wide significantly associated with elevated BMI at age 2, indicating genetic predisposition to weight gain via altered leptin signaling
Track weight and height regularly; monitor BMI changes over time