Statistical prediction of immunity to placental malaria based on multi-assay antibody data for malarial antigens

Abstract Background Plasmodium falciparum infections are especially severe in pregnant women because infected erythrocytes (IE) express VAR2CSA, a ligand that binds to placental trophoblasts, causing IE to accumulate in the placenta. Resulting inflammation and pathology increases a woman’s risk of a...

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Main Authors: Chathura Siriwardhana, Rui Fang, Ali Salanti, Rose G. F. Leke, Naveen Bobbili, Diane Wallace Taylor, John J. Chen
Format: Article
Language:English
Published: BMC 2017-09-01
Series:Malaria Journal
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12936-017-2041-3
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spelling doaj-79851938b2c54c2c8faa7542eb7198cb2020-11-25T00:22:20ZengBMCMalaria Journal1475-28752017-09-0116111210.1186/s12936-017-2041-3Statistical prediction of immunity to placental malaria based on multi-assay antibody data for malarial antigensChathura Siriwardhana0Rui Fang1Ali Salanti2Rose G. F. Leke3Naveen Bobbili4Diane Wallace Taylor5John J. Chen6Biostatistics Core, Department of Complementary and Integrative Medicine, John A. Burns School of Medicine, University of Hawaii at ManoaBiostatistics Core, Department of Complementary and Integrative Medicine, John A. Burns School of Medicine, University of Hawaii at ManoaCentre for Medical Parasitology at Department of Immunology and Microbiology, University of Copenhagen and Department of Infectious Diseases, Copenhagen University HospitalThe Biotechnology Center, Faculty of Medicine and Biomedical Research, University of Yaoundé IDepartment of Tropical Medicine, Medical Microbiology and Pharmacology, John A. Burns School of Medicine, University of Hawaii at ManoaDepartment of Tropical Medicine, Medical Microbiology and Pharmacology, John A. Burns School of Medicine, University of Hawaii at ManoaBiostatistics Core, Department of Complementary and Integrative Medicine, John A. Burns School of Medicine, University of Hawaii at ManoaAbstract Background Plasmodium falciparum infections are especially severe in pregnant women because infected erythrocytes (IE) express VAR2CSA, a ligand that binds to placental trophoblasts, causing IE to accumulate in the placenta. Resulting inflammation and pathology increases a woman’s risk of anemia, miscarriage, premature deliveries, and having low birthweight (LBW) babies. Antibodies (Ab) to VAR2CSA reduce placental parasitaemia and improve pregnancy outcomes. Currently, no single assay is able to predict if a woman has adequate immunity to prevent placental malaria (PM). This study measured Ab levels to 28 malarial antigens and used the data to develop statistical models for predicting if a woman has sufficient immunity to prevent PM. Methods Archival plasma samples from 1377 women were screened in a bead-based multiplex assay for Ab to 17 VAR2CSA-associated antigens (full length VAR2CSA (FV2), DBL 1-6 of the FCR3, 3D7 and 7G8 lines, ID1-ID2a (FCR3 and 3D7) and 11 antigens that have been reported to be associated with immunity to P. falciparum (AMA-1, CSP, EBA-175, LSA1, MSP1, MSP2, MSP3, MSP11, Pf41, Pf70 and RESA)). Ab levels along with clinical variables (age, gravidity) were used in the following seven statistical approaches: logistic regression full model, logistic regression reduced model, recursive partitioning, random forests, linear discriminant analysis, quadratic discriminant analysis, and support vector machine. Results The best and simplest model proved to be the logistic regression reduced model. AMA-1, MSP2, EBA-175, Pf41, and MSP11 were found to be the top five most important predictors for the PM status based on overall prediction performance. Conclusions Not surprising, significant differences were observed between PM positive (PM+) and PM negative (PM−) groups for Ab levels to the majority of malaria antigens. Individually though, these malarial antigens did not achieve reasonably high performances in terms of predicting the PM status. Utilizing multiple antigens in predictive models considerably improved discrimination power compared to individual assays. Among seven different classifiers considered, the reduced logistic regression model produces the best overall predictive performance.http://link.springer.com/article/10.1186/s12936-017-2041-3Predictive modelsPlacental malariaMultiplex assaysVAR2CSA
collection DOAJ
language English
format Article
sources DOAJ
author Chathura Siriwardhana
Rui Fang
Ali Salanti
Rose G. F. Leke
Naveen Bobbili
Diane Wallace Taylor
John J. Chen
spellingShingle Chathura Siriwardhana
Rui Fang
Ali Salanti
Rose G. F. Leke
Naveen Bobbili
Diane Wallace Taylor
John J. Chen
Statistical prediction of immunity to placental malaria based on multi-assay antibody data for malarial antigens
Malaria Journal
Predictive models
Placental malaria
Multiplex assays
VAR2CSA
author_facet Chathura Siriwardhana
Rui Fang
Ali Salanti
Rose G. F. Leke
Naveen Bobbili
Diane Wallace Taylor
John J. Chen
author_sort Chathura Siriwardhana
title Statistical prediction of immunity to placental malaria based on multi-assay antibody data for malarial antigens
title_short Statistical prediction of immunity to placental malaria based on multi-assay antibody data for malarial antigens
title_full Statistical prediction of immunity to placental malaria based on multi-assay antibody data for malarial antigens
title_fullStr Statistical prediction of immunity to placental malaria based on multi-assay antibody data for malarial antigens
title_full_unstemmed Statistical prediction of immunity to placental malaria based on multi-assay antibody data for malarial antigens
title_sort statistical prediction of immunity to placental malaria based on multi-assay antibody data for malarial antigens
publisher BMC
series Malaria Journal
issn 1475-2875
publishDate 2017-09-01
description Abstract Background Plasmodium falciparum infections are especially severe in pregnant women because infected erythrocytes (IE) express VAR2CSA, a ligand that binds to placental trophoblasts, causing IE to accumulate in the placenta. Resulting inflammation and pathology increases a woman’s risk of anemia, miscarriage, premature deliveries, and having low birthweight (LBW) babies. Antibodies (Ab) to VAR2CSA reduce placental parasitaemia and improve pregnancy outcomes. Currently, no single assay is able to predict if a woman has adequate immunity to prevent placental malaria (PM). This study measured Ab levels to 28 malarial antigens and used the data to develop statistical models for predicting if a woman has sufficient immunity to prevent PM. Methods Archival plasma samples from 1377 women were screened in a bead-based multiplex assay for Ab to 17 VAR2CSA-associated antigens (full length VAR2CSA (FV2), DBL 1-6 of the FCR3, 3D7 and 7G8 lines, ID1-ID2a (FCR3 and 3D7) and 11 antigens that have been reported to be associated with immunity to P. falciparum (AMA-1, CSP, EBA-175, LSA1, MSP1, MSP2, MSP3, MSP11, Pf41, Pf70 and RESA)). Ab levels along with clinical variables (age, gravidity) were used in the following seven statistical approaches: logistic regression full model, logistic regression reduced model, recursive partitioning, random forests, linear discriminant analysis, quadratic discriminant analysis, and support vector machine. Results The best and simplest model proved to be the logistic regression reduced model. AMA-1, MSP2, EBA-175, Pf41, and MSP11 were found to be the top five most important predictors for the PM status based on overall prediction performance. Conclusions Not surprising, significant differences were observed between PM positive (PM+) and PM negative (PM−) groups for Ab levels to the majority of malaria antigens. Individually though, these malarial antigens did not achieve reasonably high performances in terms of predicting the PM status. Utilizing multiple antigens in predictive models considerably improved discrimination power compared to individual assays. Among seven different classifiers considered, the reduced logistic regression model produces the best overall predictive performance.
topic Predictive models
Placental malaria
Multiplex assays
VAR2CSA
url http://link.springer.com/article/10.1186/s12936-017-2041-3
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