Evidence map›Paper›PMID 31590669›Full record

ArticleMalaria journal2019

Detection of malaria parasites in dried human blood spots using mid-infrared spectroscopy and logistic regression analysis.

Emmanuel P Mwanga, Elihaika G Minja, Emmanuel Mrimi, Mario González Jiménez, Johnson K Swai, Said Abbasi, Halfan S Ngowo, Doreen J Siria, Salum Mapua, Caleb Stica and 9 more

Open access · goldAbstract read
In one paragraph

Article in Malaria journal, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
7.1field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 67 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 5 institutions in 5 countries.

Emmanuel P MwangaEnvironmental Health and Ecological Sciences Department, Ifakara Health Institute, Morogoro, Tanzania. emwanga@ihi.or.tz.
Elihaika G MinjaEnvironmental Health and Ecological Sciences Department, Ifakara Health Institute, Morogoro, Tanzania.
Emmanuel MrimiEnvironmental Health and Ecological Sciences Department, Ifakara Health Institute, Morogoro, Tanzania.
Mario González JiménezSchool of Chemistry, University of Glasgow, Glasgow, G12 8QQ, UK.
Johnson K SwaiEnvironmental Health and Ecological Sciences Department, Ifakara Health Institute, Morogoro, Tanzania.
Said AbbasiEnvironmental Health and Ecological Sciences Department, Ifakara Health Institute, Morogoro, Tanzania.
Halfan S NgowoEnvironmental Health and Ecological Sciences Department, Ifakara Health Institute, Morogoro, Tanzania.
Doreen J SiriaEnvironmental Health and Ecological Sciences Department, Ifakara Health Institute, Morogoro, Tanzania.
Salum MapuaEnvironmental Health and Ecological Sciences Department, Ifakara Health Institute, Morogoro, Tanzania.
Caleb SticaEnvironmental Health and Ecological Sciences Department, Ifakara Health Institute, Morogoro, Tanzania.
Marta F MaiaKEMRI Wellcome Trust Research Programme, P.O. Box 230, Kilifi, 80108, Kenya.
Ally OlotuKEMRI Wellcome Trust Research Programme, P.O. Box 230, Kilifi, 80108, Kenya.
Maggy T Sikulu-LordSchool of Public Health, University of Queensland, Saint Lucia, Australia.
Francesco BaldiniInstitute of Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow, G12 8QQ, UK.
Heather M FergusonInstitute of Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow, G12 8QQ, UK.
Klaas WynneSchool of Chemistry, University of Glasgow, Glasgow, G12 8QQ, UK.
Prashanth SelvarajInstitute for Disease Modeling, Bellevue, WA, 98005, USA.
Simon A BabayanInstitute of Biodiversity, Animal Health and Comparative Medicine, University of Glasgow, Glasgow, G12 8QQ, UK.
Fredros O OkumuEnvironmental Health and Ecological Sciences Department, Ifakara Health Institute, Morogoro, Tanzania. fredros@ihi.or.tz.
Ifakara Health Institute · TZUniversity of Glasgow · GBBellevue Hospital Center · USMarquette University · USUniversity of Oxford · GB

Funding

Howard Hughes Medical Institute (US) and Bill and Melinda Gates Foundation Grant No. OPP1099295Medical Research Council Grant No. MR/P025501/1Medical Research Council MR/P025501/1Wellcome Trust Grant No. WT102350/Z/13/ZWellcome Trust WT200086/Z/15/Z
6 · The paper itself

Abstract

backgroundEpidemiological surveys of malaria currently rely on microscopy, polymerase chain reaction assays (PCR) or rapid diagnostic test kits for Plasmodium infections (RDTs). This study investigated whether mid-infrared (MIR) spectroscopy coupled with supervised machine learning could constitute an alternative method for rapid malaria screening, directly from dried human blood spots.

methodsFilter papers containing dried blood spots (DBS) were obtained from a cross-sectional malaria survey in 12 wards in southeastern Tanzania in 2018/19. The DBS were scanned using attenuated total reflection-Fourier Transform Infrared (ATR-FTIR) spectrometer to obtain high-resolution MIR spectra in the range 4000 cm

resultsLogistic regression was the best-performing model. Considering PCR as reference, the models attained overall accuracies of 92% for predicting P. falciparum infections (specificity = 91.7%; sensitivity = 92.8%) and 85% for predicting mixed infections of P. falciparum and Plasmodium ovale (specificity = 85%, sensitivity = 85%) in the field-collected specimen.

conclusionThese results demonstrate that mid-infrared spectroscopy coupled with supervised machine learning (MIR-ML) could be used to screen for malaria parasites in human DBS. The approach could have potential for rapid and high-throughput screening of Plasmodium in both non-clinical settings (e.g., field surveys) and clinical settings (diagnosis to aid case management). However, before the approach can be used, we need additional field validation in other study sites with different parasite populations, and in-depth evaluation of the biological basis of the MIR signals. Improving the classification algorithms, and model training on larger datasets could also improve specificity and sensitivity. The MIR-ML spectroscopy system is physically robust, low-cost, and requires minimum maintenance.

Indexed as

Supervised Machine LearningDried Blood Spot TestingHumansLogistic ModelsMalaria, FalciparumPlasmodium falciparumSpectrophotometry, InfraredTanzaniaAttenuated total reflection-Fourier Transform Infrared spectrometerDried blood spotsIfakara Health InstituteMalaria diagnosisMid-infrared spectroscopyPCRPlasmodiumSupervised machine learning

Identifiers

PMID31590669
PMCPMC6781347
OpenAlexW2979429529

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.