Evidence map›Paper›PMID 39770840›Full record

ArticleMicroorganisms2024

Using Catalytic Models to Interpret Age-Stratified Lyme Borreliosis Seroprevalence Data: Can This Approach Help Provide Insight into the Full Extent of Human Infection Occurring at the Population Level?

Andrew Vyse, Emily Colby

Abstract read
In one paragraph

Article in Microorganisms, 2024. 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

2 authors.

Andrew VyseMedical Affairs, Pfizer UK Ltd., Tadworth, Surrey KT20 7NS, UK.
Emily ColbyVaccines and Antivirals Medical Affairs, Pfizer US Commercial Division, New York, NY 10001-2192, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diagnosis of Lyme borreliosis (LB) is prone to under ascertainment with the true extent of infection unknown. Cross sectional age-stratified population-based serological survey data may provide insight into this issue. Using data from a previously published Dutch seroprevalence study, we describe the application of catalytic models to make estimates of the annual extent of LB infection. A common assumption when using catalytic models is that IgG is protective and immunity is lifelong. However, human IgG produced in response to natural LB infection does not protect against subsequent infection and its duration may be limited. Individuals were thus assumed to be continually susceptible to LB infection, with a range of scenarios used that varied the length of time that IgG may remain detectable, from 5 years post-infection to lifelong. The possibility that IgG may remain detectable for longer in adults than in children was also explored. Estimates for the annual number of LB infections occurring in the Dutch population ranged from 163,265 (95%CI 130,150-201,723) when assuming IgG remains detectable for only 5 years post-infection to 26,209 (95%CI 17,159-36,557) when assuming IgG is lifelong.

Indexed as

catalytic modelsinfectionLyme borreliosisseroprevalence

Identifiers

PMID39770840
PMCPMC11678136

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.