Evidence map›Paper›PMID 30689671›Full record

Trial reportPLoS neglected tropical diseases2019

Community-level chlamydial serology for assessing trachoma elimination in trachoma-endemic Niger.

Jessica S Kim, Catherine E Oldenburg, Gretchen Cooley, Abdou Amza, Boubacar Kadri, Baido Nassirou, Sun Yu Cotter, Nicole E Stoller, Sheila K West, Robin L Bailey and 5 more

Registry-linked trialAbstract readRandomized Controlled Trial
In one paragraph

Trial report in PLoS neglected tropical diseases, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00792922 (Research to Programs for Trachoma Elimination), which is not on this map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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.

NCT00792922 phase4completednot on this map

Research to Programs for Trachoma Elimination: Antibiotic Trial

TypeinterventionalSponsorJohns Hopkins UniversityRan2008 to 2014Enrolled128ConditionsTrachomaArmsAzithromycin
3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Trial
  2. Article
  3. Data Resource Profile: Global Trachoma Serology Data Repository.International journal of epidemiology · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Monitoring transmission intensity of trachoma with serology.medRxiv : the preprint server for health sciences · 2023
    Article
  8. Trachoma.Nature reviews. Disease primers · 2022
    Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
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

15 authors.

Jessica S KimF. I. Proctor Foundation, University of California San Francisco, San Francisco, California, United States of America.
Catherine E OldenburgF. I. Proctor Foundation, University of California San Francisco, San Francisco, California, United States of America.ORCID 0000-0002-0763-399X
Gretchen CooleyDivison of Parasitic Diseases and Malaria, Centers for Disease Prevention and Control, Atlanta, Georgia, United States of America.
Abdou AmzaProgramme FSS/Université Abdou Moumouni de Niamey, Programme Nationale des Soins Oculaire, Niger.
Boubacar KadriProgramme FSS/Université Abdou Moumouni de Niamey, Programme Nationale des Soins Oculaire, Niger.
Baido NassirouProgramme FSS/Université Abdou Moumouni de Niamey, Programme Nationale des Soins Oculaire, Niger.
Sun Yu CotterF. I. Proctor Foundation, University of California San Francisco, San Francisco, California, United States of America.
Nicole E StollerF. I. Proctor Foundation, University of California San Francisco, San Francisco, California, United States of America.
Sheila K WestDana Center for Preventive Ophthalmology, Wilmer Eye Institute, Johns Hopkins University, Baltimore, Maryland, United States of America.
Robin L BaileyClinical Research Unit, Department of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Jeremy D KeenanF. I. Proctor Foundation, University of California San Francisco, San Francisco, California, United States of America.
Bruce D GaynorF. I. Proctor Foundation, University of California San Francisco, San Francisco, California, United States of America.
Travis C PorcoF. I. Proctor Foundation, University of California San Francisco, San Francisco, California, United States of America.
Thomas M LietmanF. I. Proctor Foundation, University of California San Francisco, San Francisco, California, United States of America.
Diana L MartinDivison of Parasitic Diseases and Malaria, Centers for Disease Prevention and Control, Atlanta, Georgia, United States of America.ORCID 0000-0001-9417-5562

Funding

The Brown Initiative in HIV and AIDS Clinical Research for Minority CommunitiesR25MH083620 · NIMH · MIRIAM HOSPITAL · PI NUNN, AMY STEWART · 2008 to 2025
$3.7M
NIMH NIH HHS R25 MH083620
6 · The paper itself

Abstract

backgroundProgram decision-making for trachoma elimination currently relies on conjunctival clinical signs. Antibody tests may provide additional information on the epidemiology of trachoma, particularly in regions where it is disappearing or elimination targets have been met.

methodsA cluster-randomized trial of mass azithromycin distribution strategies for trachoma elimination was conducted over three years in a mesoendemic region of Niger. Dried blood spots were collected from a random sample of children aged 1-5 years in each of 24 study communities at 36 months after initiation of the intervention. A multiplex bead assay was used to test for antibodies to two Chlamydia trachomatis antigens, Pgp3 and CT694. We compared seropositivity to either antigen to clinical signs of active trachoma (trachomatous inflammation-follicular [TF] and trachomatous inflammation-intense [TI]) at the individual and cluster level, and to ocular chlamydia prevalence at the community level.

resultsOf 988 children with antibody data, TF prevalence was 7.8% (95% CI 6.1 to 9.5) and TI prevalence was 1.6% (95% CI 0.9 to 2.6). The overall prevalence of antibody positivity to Pgp3 was 27.2% (95% CI 24.5 to 30), and to CT694 was 23.7% (95% CI 21 to 26.2). Ocular chlamydia infection prevalence was 5.2% (95% CI 2.8 to 7.6). Seropositivity to Pgp3 and/or CT694 was significantly associated with TF at the individual and community level and with ocular chlamydia infection and TI at the community level. Older children were more likely to be seropositive than younger children.

conclusionSeropositivity to Pgp3 and CT694 correlates with clinical signs and ocular chlamydia infection in a mesoendemic region of Niger.

trial registrationClinicalTrials.gov NCT00792922.

Indexed as

Disease EradicationMass Drug AdministrationAnti-Bacterial AgentsAntibodies, BacterialAntigens, BacterialAzithromycinBacterial ProteinsChild, PreschoolChlamydia trachomatisDNA, BacterialEndemic DiseasesHumansInfantInfant, NewbornNigerTrachomaAnti-Bacterial AgentsAntibodies, BacterialAntigens, BacterialAzithromycinBacterial ProteinsCT694 protein, Chlamydia trachomatisDNA, Bacterialpgp3 protein, Chlamydia

Identifiers

PMID30689671
PMCPMC6366708

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Registered trials

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.