The evolutionary and clinical implilcations of the uneven distribution of the frequency of the inherited haemoglobin variants over short geographical distances
Author(s)
Type
Journal Article
Abstract
Studies of the frequency of heterozygous carriers for common inherited
diseases of haemoglobin in over 7500 adolescent children in 25 districts in
Sri Lanka have disclosed a highly significant variation over very short geo-
graphical distances. A further analysis of these findings, including their
relationship to the past frequency and distribution of malaria, climatic vari-
ation, altitude, ethnic origin and consanguinity rates, have provided evi-
dence regarding the evolutionary basis for the variable distribution of these
conditions over short distances. It is likely that the complex interplay
between malaria and the environment, together with related ethnic and
social issues, exists in many countries across the tropical belt. Hence, these
observations emphasise the importance of micromapping heterozygote dis-
tributions in high-frequency countries in order to define their true burden
and the facilities required for the prevention and management of the
homozygous and compound heterozygous disorders that result from their
interaction.
diseases of haemoglobin in over 7500 adolescent children in 25 districts in
Sri Lanka have disclosed a highly significant variation over very short geo-
graphical distances. A further analysis of these findings, including their
relationship to the past frequency and distribution of malaria, climatic vari-
ation, altitude, ethnic origin and consanguinity rates, have provided evi-
dence regarding the evolutionary basis for the variable distribution of these
conditions over short distances. It is likely that the complex interplay
between malaria and the environment, together with related ethnic and
social issues, exists in many countries across the tropical belt. Hence, these
observations emphasise the importance of micromapping heterozygote dis-
tributions in high-frequency countries in order to define their true burden
and the facilities required for the prevention and management of the
homozygous and compound heterozygous disorders that result from their
interaction.
Date Issued
2016-11-29
Date Acceptance
2016-08-23
Citation
British Journal of Haematology, 2016, 176 (3), pp.475-484
ISSN
1365-2141
Publisher
Wiley
Start Page
475
End Page
484
Journal / Book Title
British Journal of Haematology
Volume
176
Issue
3
Copyright Statement
© 2016 John Wiley & Sons Ltd. "This is the peer reviewed version of the following article, which has been published in final form at:http://onlinelibrary.wiley.com/doi/10.1111/bjh.14437/abstract. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.
Subjects
consanguinity
distribution
haemoglobinopathies
malaria
micromapping
Adolescent
Altitude
Climate
Consanguinity
Ethnic Groups
Evolution, Molecular
Female
Genetic Variation
Hemoglobinopathies
Hemoglobins
Heterozygote
Humans
Malaria
Male
Molecular Epidemiology
Sri Lanka
Immunology
1102 Cardiovascular Medicine And Haematology
Publication Status
Published