Evidence map›Paper›PMID 38917816›Full record

ArticleThe American journal of tropical medicine and hygiene2024

Integrated Serosurveillance for Onchocerciasis, Lymphatic Filariasis, and Schistosomiasis in North Darfur, Sudan.

Jenna E Coalson, Gregory S Noland, Andrew W Nute, Erica Brook Goodhew, Diana L Martin, Zeinab Abdalla, Isam Zarroug, Soheir Gabralla, Hassan Ahmed Hassan Ahmed Ismail, William Evan Secor and 4 more

Abstract read
In one paragraph

Article in The American journal of tropical medicine and hygiene, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
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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

14 authors.

Jenna E CoalsonRiver Blindness, Lymphatic Filariasis, Schistosomiasis, and Malaria Programs, The Carter Center, Atlanta, Georgia.
Gregory S NolandRiver Blindness, Lymphatic Filariasis, Schistosomiasis, and Malaria Programs, The Carter Center, Atlanta, Georgia.
Andrew W NuteTrachoma Control Program, The Carter Center, Atlanta, Georgia.
Erica Brook GoodhewLaboratory Science and Diagnostics Branch, Division of Parasitic Diseases and Malaria, U.S. Centers for Disease Control and Prevention, Atlanta, Georgia.
Diana L MartinLaboratory Science and Diagnostics Branch, Division of Parasitic Diseases and Malaria, U.S. Centers for Disease Control and Prevention, Atlanta, Georgia.
Zeinab AbdallaHealth Programs, The Carter Center, Khartoum, Sudan.
Isam ZarrougHealth Programs, The Carter Center, Khartoum, Sudan.
Soheir GabrallaFederal Ministry of Health, Khartoum, Sudan.
Hassan Ahmed Hassan Ahmed IsmailFederal Ministry of Health, Khartoum, Sudan.
William Evan SecorLaboratory Science and Diagnostics Branch, Division of Parasitic Diseases and Malaria, U.S. Centers for Disease Control and Prevention, Atlanta, Georgia.
Elizabeth Kelly CallahanTrachoma Control Program, The Carter Center, Atlanta, Georgia.
Angelia M SandersTrachoma Control Program, The Carter Center, Atlanta, Georgia.
Balgesa ElshafieFederal Ministry of Health, Khartoum, Sudan.
Scott D NashTrachoma Control Program, The Carter Center, Atlanta, Georgia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sudan is endemic for multiple neglected tropical diseases, including trachoma, onchocerciasis (OV), lymphatic filariasis (LF), and schistosomiasis (SCH). In 2019, dried blood spot samples were collected for a baseline trachoma serosurvey in three localities (El Seraif, Kotom, and Saraf Omrah) in North Darfur State. None were classified previously as OV- or LF-endemic, although low levels of SCH had been identified in all three. Approximately 30 households from 25 communities in each locality were selected by multistage cluster random sampling. Collections of DBSs were analyzed by multiplex bead assay for antibodies to multiple pathogens. This paper presents data on OV (Ov16), LF (Wb123, Bm14, Bm33), and SCH (soluble egg antigen [SEA], Sm25) antibodies among 8,322 individuals from 2,119 households. The survey-adjusted seroprevalence estimates for Ov16 were <0.3% in all localities. Lymphatic filariasis-antigen seroprevalences were discordant. Seroprevalence estimates ranged from 4.6-6.0% (Wb123), 0.99-1.4% (Bm14), and 29.2-33.3% (Bm33). Schistosomiasis seroprevalence estimates among school-aged children ranged from 2.7-8.0% (SEA) and 10.9-15.6% (Sm25). Ov16 seropositivity was low and supported the localities' classification as nonendemic. The results suggested LF exposure, but discordance between antigens, challenges defining seropositivity thresholds, and the absence of programmatic guidance based on antibody serology alone for Wuchereria bancrofti indicate a need for remapping surveys to confirm transmission. Schistosomiasis antibody levels were high enough to warrant further mapping to guide treatment decisions. The lack of gold standards limited interpretation of results, particularly for LF, but in resource-challenged areas, integrated serological surveillance offers the possibility of efficient monitoring of exposure to multiple diseases.

Indexed as

Elephantiasis, FilarialOnchocerciasisSchistosomiasisAdolescentAdultAgedAnimalsAntibodies, HelminthChildChild, PreschoolFemaleHumansInfantMaleMiddle AgedSeroepidemiologic StudiesAntibodies, Helminth

Identifiers

PMID38917816
PMCPMC11376112

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LicenceCC BY
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Registered trials

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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.