Evidence map›Paper›PMID 42723761›Full record

SynthesisWellcome open research2026

Sero-epidemiological studies of pathogen burden: A scoping review.

Anne Suffel, Danny Turton, Kathryin E Mansfield, Alexander J Mentzer, Naomi E Allen, Aisha Babi, David Burgner, Tim Waterboer, Charlotte Warren-Gash

Abstract readSystematic Review
In one paragraph

Synthesis in Wellcome open research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Anne SuffelDepartment of Non-Communicable Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, England, UK.ORCID https://orcid.org/0000-0002-9021-0487
Danny TurtonDepartment of Non-Communicable Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, England, UK.
Kathryin E MansfieldSchool of Health and Care Sciences, University of Lincoln, Lincoln, England, UK.
Alexander J MentzerCentre for Human Genetics, University of Oxford, Oxford, England, UK.ORCID https://orcid.org/0000-0002-4502-2209
Naomi E AllenNuffield Department of Population Health, University of Oxford, Oxford, England, UK.ORCID https://orcid.org/0000-0003-1938-5038
Aisha BabiGerman Cancer Research Center, Heidelberg, Baden-Württemberg, Germany.ORCID https://orcid.org/0000-0002-2726-6955
David BurgnerRoyal Children's Hospital, Murdoch Children's Research Institute, Parkville, Victoria, Australia.ORCID https://orcid.org/0000-0002-8304-4302
Tim WaterboerGerman Cancer Research Center, Heidelberg, Baden-Württemberg, Germany.
Charlotte Warren-GashDepartment of Non-Communicable Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, England, UK.ORCID https://orcid.org/0000-0003-4524-3180

Funding

Wellcome Trust
6 · The paper itself

Abstract

Background: Methodological advances in serological testing have made it feasible to quantify antibodies to multiple pathogens simultaneously. This has been used to study the impact of pathogen burden, i.e., cumulative lifetime exposure to persistent pathogens, on health and mortality outcomes. However, definitions for pathogen burden using serological data vary considerably. It is unclear how to best combine serological data for multiple pathogens for exposure/outcome definitions in epidemiological studies. Methods: Following PRISMA-ScR guidelines, we conducted a scoping review of all relevant publications from MEDLINE, Embase, and Scopus until May 1 Results: We included a total of 74 studies from 19 countries (published 2000-2025). Serology data from 50 different pathogens were analysed across all studies, with pathogen burden measured by combining a range of 3-17 pathogens across studies into a single metric. Approaches included counts of seropositive result, quantiles of antibody titres, and more complex statistical analyses to group pathogens. No study gave a clinical/scientific rationale for the approaches chosen. Conclusions: Various analytical approaches have been used to define pathogen burden but there was limited justification for the chosen methodological approaches. More integrated approaches are needed for combining scientific and clinical knowledge of the interaction across different pathogens and epidemiological evidence into a meaningful measure of pathogen burden.

Indexed as

infectionspathogen burden; serology

Identifiers

PMID42723761
PMCPMC13554841

What OpenQuestion holds

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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.