Helmholtz Gemeinschaft

Search
Browse
Statistics
Feeds

Genome-wide linkage analysis of malaria infection intensity and mild disease

[img] PDF - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader
353kB

Item Type:Article
Title:Genome-wide linkage analysis of malaria infection intensity and mild disease
Creators Name:Timmann, C. and Evans, J.A. and Koenig, I.R. and Kleensang, A. and Ruschendorf, F. and Lenzen, J. and Sievertsen, J. and Becker, C. and Enuameh, Y. and Kwakye, K.O. and Opoku, E. and Browne, E.N. and Ziegler, A. and Nurnberg, P. and Horstmann, R.D.
Abstract:Although balancing selection with the sickle-cell trait and other red blood cell disorders has emphasized the interaction between malaria and human genetics, no systematic approach has so far been undertaken towards a comprehensive search for human genome variants influencing malaria. By screening 2,551 families in rural Ghana, West Africa, 108 nuclear families were identified who were exposed to hyperendemic malaria transmission and were homozygous wild-type for the established malaria resistance factors of hemoglobin (Hb)S, HbC, alpha(+) thalassemia, and glucose-6-phosphate-dehydrogenase deficiency. Of these families, 392 siblings aged 0.5-11 y were characterized for malaria susceptibility by closely monitoring parasite counts, malaria fever episodes, and anemia over 8 mo. An autosome-wide linkage analysis based on 10,000 single-nucleotide polymorphisms was conducted in 68 selected families including 241 siblings forming 330 sib pairs. Several regions were identified which showed evidence for linkage to the parasitological and clinical phenotypes studied, among them a prominent signal on Chromosome 10p15 obtained with malaria fever episodes (asymptotic z score = 4.37, empirical p-value = 4.0 x 10(-5), locus-specific heritability of 37.7%; 95% confidence interval, 15.7%-59.7%). The identification of genetic variants underlying the linkage signals may reveal as yet unrecognized pathways influencing human resistance to malaria
Keywords:African Continental Ancestry Group, Chromosomes, Human, Pair 10, Cohort Studies, Endemic Diseases, Genetic Markers, Genotype, Lod Score, Malaria, Oligonucleotide Array Sequence Analysis, Parasitemia, Single Nucleotide Polymorphism, Prevalence, Rural Population, Severity of Illness Index, Siblings
Source:PLoS Genetics
ISSN:1553-7390
Publisher:Public Library of Science
Volume:3
Number:3
Page Range:393-400
Date:23 March 2007
Official Publication:https://doi.org/10.1371/journal.pgen.0030048
PubMed:View item in PubMed

Repository Staff Only: item control page

Downloads

Downloads per month over past year

Open Access
MDC Library