<HashMap><database>biostudies-literature</database><scores/><additional><submitter>McQuillan MA</submitter><funding>University of Pennsylvania Center of Excellence in Environmental Toxicology</funding><funding>NIDDK NIH HHS</funding><funding>University of Pennsylvania</funding><funding>NIEHS NIH HHS</funding><funding>American Diabetes Association</funding><funding>National Institutes of Health</funding><funding>NIGMS NIH HHS</funding><pagination>927-938</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11080607</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>111(5)</volume><pubmed_abstract>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 neg</pubmed_abstract><journal>American journal of human genetics</journal><pubmed_title>Association between telomere length and Plasmodium falciparum malaria endemicity in sub-Saharan Africans.</pubmed_title><pmcid>PMC11080607</pmcid><funding_grant_id>T32-ES019851</funding_grant_id><funding_grant_id>R35 GM134957-01</funding_grant_id><funding_grant_id>P30 DK019525</funding_grant_id><funding_grant_id>R35 GM134957</funding_grant_id><funding_grant_id>T32 ES019851</funding_grant_id><funding_grant_id>1-19-VSN-02</funding_grant_id><pubmed_authors>Chanock SJ</pubmed_authors><pubmed_authors>Njamnshi AK</pubmed_authors><pubmed_authors>Hansen MEB</pubmed_authors><pubmed_authors>McQuillan MA</pubmed_authors><pubmed_authors>Meskel DW</pubmed_authors><pubmed_authors>Tishkoff SA</pubmed_authors><pubmed_authors>Fokunang C</pubmed_authors><pubmed_authors>Beggs W</pubmed_authors><pubmed_authors>Verhulst S</pubmed_authors><pubmed_authors>Aviv A</pubmed_authors><pubmed_authors>Nyambo T</pubmed_authors><pubmed_authors>Mpoloka SW</pubmed_authors><pubmed_authors>Mokone GG</pubmed_authors><pubmed_authors>Belay G</pubmed_authors></additional><is_claimable>false</is_claimable><name>Association between telomere length and Plasmodium falciparum malaria endemicity in sub-Saharan Africans.</name><description>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 neg</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 May</publication><modification>2026-06-02T04:08:39.005Z</modification><creation>2025-04-21T21:44:30.792Z</creation></dates><accession>S-EPMC11080607</accession><cross_references><pubmed>38701745</pubmed><doi>10.1016/j.ajhg.2024.04.003</doi></cross_references></HashMap>