TY - JOUR
T1 - Association between telomere length and Plasmodium falciparum malaria endemicity in sub-Saharan Africans
AU - McQuillan, Michael A.
AU - Verhulst, Simon
AU - Hansen, Matthew E.B.
AU - Beggs, William
AU - Meskel, Dawit Wolde
AU - Belay, Gurja
AU - Nyambo, Thomas
AU - Mpoloka, Sununguko Wata
AU - Mokone, Gaonyadiwe George
AU - Fokunang, Charles
AU - Njamnshi, Alfred K.
AU - Chanock, Stephen J.
AU - Aviv, Abraham
AU - Tishkoff, Sarah A.
N1 - Publisher Copyright:
© 2024 American Society of Human Genetics
PY - 2024/5/2
Y1 - 2024/5/2
N2 - Leukocyte telomere length (LTL) varies significantly across human populations, with individuals of African ancestry having longer LTL than non-Africans. However, the genetic and environmental drivers of LTL variation in Africans remain largely unknown. We report here on the relationship between LTL, genetics, and a variety of environmental and climatic factors in ethnically diverse African adults (n = 1,818) originating from Botswana, Tanzania, Ethiopia, and Cameroon. We observe significant variation in LTL among populations, finding that the San hunter-gatherers from Botswana have the longest leukocyte telomeres and that the Fulani pastoralists from Cameroon have the shortest telomeres. Genetic factors explain ∼50% of LTL variation among individuals. Moreover, we observe a significant negative association between Plasmodium falciparum malaria endemicity and LTL while adjusting for age, sex, and genetics. Within Africa, adults from populations indigenous to areas with high malaria exposure have shorter LTL than those in populations indigenous to areas with low malaria exposure. Finally, we explore to what degree the genetic architecture underlying LTL in Africa covaries with malaria exposure.
AB - Leukocyte telomere length (LTL) varies significantly across human populations, with individuals of African ancestry having longer LTL than non-Africans. However, the genetic and environmental drivers of LTL variation in Africans remain largely unknown. We report here on the relationship between LTL, genetics, and a variety of environmental and climatic factors in ethnically diverse African adults (n = 1,818) originating from Botswana, Tanzania, Ethiopia, and Cameroon. We observe significant variation in LTL among populations, finding that the San hunter-gatherers from Botswana have the longest leukocyte telomeres and that the Fulani pastoralists from Cameroon have the shortest telomeres. Genetic factors explain ∼50% of LTL variation among individuals. Moreover, we observe a significant negative association between Plasmodium falciparum malaria endemicity and LTL while adjusting for age, sex, and genetics. Within Africa, adults from populations indigenous to areas with high malaria exposure have shorter LTL than those in populations indigenous to areas with low malaria exposure. Finally, we explore to what degree the genetic architecture underlying LTL in Africa covaries with malaria exposure.
KW - Africa
KW - malaria
KW - population genetics
KW - telomere
UR - http://www.scopus.com/inward/record.url?scp=85191201892&partnerID=8YFLogxK
U2 - 10.1016/j.ajhg.2024.04.003
DO - 10.1016/j.ajhg.2024.04.003
M3 - Article
C2 - 38701745
AN - SCOPUS:85191201892
SN - 0002-9297
VL - 111
SP - 927
EP - 938
JO - American Journal of Human Genetics
JF - American Journal of Human Genetics
IS - 5
ER -