Evidence map›Paper›PMID 40055638›Full record

ArticleBMC medical research methodology2025

Modeling the temporal prevalence peak drift of chronic diseases.

Jürgen Rodenkirchen, Annika Hoyer, Ralph Brinks

Abstract read
In one paragraph

Article in BMC medical research methodology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

3 authors.

Jürgen RodenkirchenBiostatistics and Medical Biometry, Medical School OWL, Bielefeld University, Universitätsstr. 25, Bielefeld, 33615, Germany. juergen.rodenkirchen@uni-bielefeld.de.
Annika Hoyer *Biostatistics and Medical Biometry, Medical School OWL, Bielefeld University, Universitätsstr. 25, Bielefeld, 33615, Germany.
Ralph Brinks *Chair for Medical Biometry and Epidemiology, Faculty of Health/School of Medicine, Witten/Herdecke University, Alfred-Herrhausen-Str. 50, Witten, 58455, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic diseases, such as type 2 diabetes, are responsible for a substantial proportion of global deaths and are marked by an increasing number of people that suffer from them. Our objective is to systematically investigate the analytical determination of the drift in prevalence peaks over calendar-time and age, with an emphasis on understanding the intrinsic attributes of temporal displacement. This aims to enhance the understanding of disease dynamics that may contribute to refining medical strategies and to plan future healthcare activities.

methodsWe present two distinct yet complementary approaches for identifying and estimating drifts in prevalence peaks. First, assuming incidence and mortality rates are known, we employ a partial differential equation that relates prevalence, incidence, and mortality. From this, we derive an ordinary differential equation to mathematically describe the prevalence peak drift. Second, assuming prevalence data (rather than incidence and mortality data) are available, we establish a logistic function approach to estimate the prevalence peak drift. We applied this method to data on the prevalence of type 2 diabetes in Germany.

resultsThe first approach provides an exact mathematical prescription of the trajectory of the prevalence peak drift over time and age, assuming incidence and mortality rates are known. In contrast, the second approach, a practical application based on available prevalence data, demonstrates the prevalence peak dynamics in a real-world scenario. The theoretical model, together with the practical application, effectively substantiates the understanding of prevalence peak dynamics in two different scenarios.

conclusionOur study shows the theoretical derivation and determination of prevalence peak drifts. Our findings underpin the dynamic nature of chronic disease prevalence, highlighting the importance of considering the related age-dependent trends for planning future healthcare activities.

Indexed as

Diabetes Mellitus, Type 2AdultAgedChronic DiseaseFemaleGermanyHumansIncidenceMaleMiddle AgedPrevalenceIllness-death modelImplicit function theoremIncidenceLexis planeLogistic functionMortalityPrevalenceRicatti equationTransport equation

Identifiers

PMID40055638
PMCPMC11887115

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.