Genetic Determinants of Telomere Length in African American Youth

Autor: Jonathan Witonsky, Marquitta J. White, Kirsten Bibbins-Domingo, Jennifer R. Elhawary, Adam Davis, Joaquin Magana, Harold J. Farber, Donglei Hu, Scott Huntsman, Maria G. Contreras, Eunice Y. Lee, Emerita Brigino-Buenaventura, Oona Risse-Adams, Kevin L. Keys, Lesly-Anne Samedy, Angel C.Y. Mak, Sam S. Oh, Sandra Salazar, Michael A. LeNoir, Andrew M. Zeiger, Celeste Eng, Pagé C. Goddard, Esteban G. Burchard, Kelley Meade, Luisa N. Borrell
Rok vydání: 2018
Předmět:
0301 basic medicine
Male
lcsh:Medicine
Genome-wide association study
Disease
0302 clinical medicine
Polymorphism (computer science)
2.1 Biological and endogenous factors
Young adult
Aetiology
lcsh:Science
Child
Pediatric
African american
Genetics
African Americans
0303 health sciences
education.field_of_study
Multidisciplinary
Single Nucleotide
Telomere
Female
Asian Continental Ancestry Group
Adolescent
Population
European Continental Ancestry Group
Quantitative trait locus
Biology
Polymorphism
Single Nucleotide

Article
White People
03 medical and health sciences
Young Adult
Asian People
Clinical Research
Humans
Genetic Predisposition to Disease
Polymorphism
education
030304 developmental biology
Human Genome
lcsh:R
Genetic variants
Chromosome
Genetic Variation
Telomere Homeostasis
Black or African American
030104 developmental biology
Genetic marker
lcsh:Q
030217 neurology & neurosurgery
Demography
Genome-Wide Association Study
Zdroj: Scientific reports, vol 8, iss 1
Scientific Reports, Vol 8, Iss 1, Pp 1-9 (2018)
Scientific Reports
Popis: Telomere length (TL) is associated with numerous disease states and is affected by genetic and environmental factors. However, TL has been mostly studied in adult populations of European or Asian ancestry. These studies have identified 34 TL-associated genetic variants recently used as genetic proxies for TL. The generalizability of these associations to pediatric populations and racially diverse populations, specifically of African ancestry, remains unclear. Furthermore, six novel variants associated with TL in a population of European children have been identified but not validated. We measured TL from whole blood samples of 492 healthy African American youth (children and adolescents between 8 and 20 years old) and performed the first genome-wide association study of TL in this population. We were unable to replicate neither the 34 reported genetic associations found in adults nor the six genetic associations found in European children. However, we discovered a novel genome-wide significant association between TL and rs1483898 on chromosome 14. Our results underscore the importance of examining these genetic associations with TL in diverse pediatric populations such as African Americans.
Databáze: OpenAIRE