Natural History of Malaria Infections During Early Childhood in Twins.
hemoglobin S
infection
malaria
pathogenesis
twins
Journal
The Journal of infectious diseases
ISSN: 1537-6613
Titre abrégé: J Infect Dis
Pays: United States
ID NLM: 0413675
Informations de publication
Date de publication:
11 01 2023
11 01 2023
Historique:
received:
28
02
2022
accepted:
15
07
2022
pubmed:
19
7
2022
medline:
14
1
2023
entrez:
18
7
2022
Statut:
ppublish
Résumé
The frequency and clinical presentation of malaria infections show marked heterogeneity in epidemiological studies. However, deeper understanding of this variability is hampered by the difficulty in quantifying all relevant factors. Here, we report the history of malaria infections in twins, who are exposed to the same in utero milieu, share genetic factors, and are similarly exposed to vectors. Data were obtained from a Malian longitudinal birth cohort. Samples from 25 twin pairs were examined for malaria infection and antibody responses. Bayesian models were developed for the number of infections during follow-up. In 16 of 25 pairs, both children were infected and often developed symptoms. In 8 of 25 pairs, only 1 twin was infected, but usually only once or twice. Statistical models suggest that this pattern is not inconsistent with twin siblings having the same underlying infection rate. In a pair with discordant hemoglobin genotype, parasite densities were consistently lower in the child with hemoglobin AS, but antibody levels were similar. By using a novel design, we describe residual variation in malaria phenotypes in naturally matched children and confirm the important role of environmental factors, as suggested by the between-twin pair heterogeneity in malaria history.
Sections du résumé
BACKGROUND
The frequency and clinical presentation of malaria infections show marked heterogeneity in epidemiological studies. However, deeper understanding of this variability is hampered by the difficulty in quantifying all relevant factors. Here, we report the history of malaria infections in twins, who are exposed to the same in utero milieu, share genetic factors, and are similarly exposed to vectors.
METHODS
Data were obtained from a Malian longitudinal birth cohort. Samples from 25 twin pairs were examined for malaria infection and antibody responses. Bayesian models were developed for the number of infections during follow-up.
RESULTS
In 16 of 25 pairs, both children were infected and often developed symptoms. In 8 of 25 pairs, only 1 twin was infected, but usually only once or twice. Statistical models suggest that this pattern is not inconsistent with twin siblings having the same underlying infection rate. In a pair with discordant hemoglobin genotype, parasite densities were consistently lower in the child with hemoglobin AS, but antibody levels were similar.
CONCLUSIONS
By using a novel design, we describe residual variation in malaria phenotypes in naturally matched children and confirm the important role of environmental factors, as suggested by the between-twin pair heterogeneity in malaria history.
Identifiants
pubmed: 35849702
pii: 6645931
doi: 10.1093/infdis/jiac294
pmc: PMC10202434
doi:
Types de publication
Journal Article
Twin Study
Research Support, N.I.H., Intramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
171-178Subventions
Organisme : Intramural NIH HHS
Pays : United States
Commentaires et corrections
Type : CommentIn
Informations de copyright
Published by Oxford University Press on behalf of Infectious Diseases Society of America 2022.
Déclaration de conflit d'intérêts
Potential conflicts of interest. All authors: No reported conflicts. All authors have submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Conflicts that the editors consider relevant to the content of the manuscript have been disclosed.
Références
Lancet Infect Dis. 2012 Jun;12(6):457-68
pubmed: 22445352
J Infect Dis. 1995 Jul;172(1):316-9
pubmed: 7797941
Sci Rep. 2017 Oct 24;7(1):13872
pubmed: 29066816
Nature. 2020 Jun;582(7810):104-108
pubmed: 32427965
PLoS One. 2012;7(9):e45542
pubmed: 23029082
BMC Med. 2015 Aug 06;13:183
pubmed: 26248615
J Infect Dis. 2005 Mar 1;191(5):799-804
pubmed: 15688298
Proc Natl Acad Sci U S A. 2000 Nov 7;97(23):12661-6
pubmed: 11035799
Elife. 2018 Jan 23;7:
pubmed: 29357976
Science. 2014 May 23;344(6186):871-7
pubmed: 24855263
Hum Genet. 2020 Jun;139(6-7):801-811
pubmed: 32130487
PLoS Med. 2005 Dec;2(12):e407
pubmed: 16259531
Am J Trop Med Hyg. 1994 Aug;51(2):123-37
pubmed: 8074247
Infect Immun. 2013 May;81(5):1491-501
pubmed: 23429537
PLoS Med. 2005 Dec;2(12):e340
pubmed: 16259530
N Engl J Med. 2014 May 8;370(19):1799-808
pubmed: 24806160
Epidemics. 2011 Jun;3(2):109-18
pubmed: 21624782
PLoS One. 2009 Oct 08;4(10):e7381
pubmed: 19812685
Protein Expr Purif. 2006 Nov;50(1):58-67
pubmed: 16884920
Am J Epidemiol. 1997 Nov 15;146(10):826-31
pubmed: 9384203
PLoS One. 2008 May 21;3(5):e2196
pubmed: 18493319