Evidence map›Paper›PMID 35276013›Full record

ArticleClinical pharmacology and therapeutics2022

Leveraging Real-World Data for EMA Qualification of a Model-Based Biomarker Tool to Optimize Type-1 Diabetes Prevention Studies.

Jagdeep T Podichetty, Patrick Lang, Inish M O'Doherty, Sarah E David, Rhoda N Muse, Stephen R Karpen, Laura Sue Song, Klaus Romero, Jackson K Burton, Type-1 Diabetes Consortium (T1DC)

Open access · hybridAbstract read
In one paragraph

Article in Clinical pharmacology and therapeutics, 2022. 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
1.9field-weighted citation impact, top 14% of its field
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, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
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

10 authors at 1 institution in 1 country.

Jagdeep T PodichettyCritical Path Institute, Tucson, Arizona, USA.
Patrick LangCritical Path Institute, Tucson, Arizona, USA.
Inish M O'DohertyCritical Path Institute, Tucson, Arizona, USA.
Sarah E DavidCritical Path Institute, Tucson, Arizona, USA.
Rhoda N MuseCritical Path Institute, Tucson, Arizona, USA.
Stephen R KarpenCritical Path Institute, Tucson, Arizona, USA.
Laura Sue SongCritical Path Institute, Tucson, Arizona, USA.
Klaus RomeroCritical Path Institute, Tucson, Arizona, USA.
Jackson K BurtonCritical Path Institute, Tucson, Arizona, USA.
Type-1 Diabetes Consortium (T1DC)
Critical Path Institute · US

Funding

Critical Path to Public Private PartnershipsU18FD005320 · FDA · CRITICAL PATH INSTITUTE · PI Klaus Romero · 2014 to 2026
$127.1M
FDA HHS U18 FD005320
6 · The paper itself

Abstract

The development of therapies to prevent or delay the onset of type 1 diabetes (T1D) remains challenging, and there is a lack of qualified biomarkers to identify individuals at risk of developing T1D or to quantify the time-varying risk of conversion to a diagnosis of T1D. To address this drug development need, the T1D Consortium (i) acquired, remapped, integrated, and curated existing patient-level data from relevant observational studies, and (ii) used a model-based approach to evaluate the utility of islet autoantibodies (AAs) against insulin/proinsulin autoantibody, GAD65, IA-2, and ZnT8 as biomarkers to enrich subjects for T1D prevention. The aggregated dataset was used to construct an accelerated failure time model for predicting T1D diagnosis. The model quantifies presence of islet AA permutations as statistically significant predictors of the time-varying probability of conversion to a diagnosis of T1D. Additional sources of variability that greatly improved the accuracy of quantifying the time-varying probability of conversion to a T1D diagnosis included baseline age, sex, blood glucose measurements from the 120-minute timepoints of oral glucose tolerance tests, and hemoglobin A1c. The developed models represented the underlying evidence to qualify islet AAs as enrichment biomarkers through the qualification of novel methodologies for drug development pathway at the European Medicines Agency (EMA). Additionally, the models are intended as the foundation of a fully functioning end-user tool that will allow sponsors to optimize enrichment criteria for clinical trials in T1D prevention studies.

Indexed as

Diabetes Mellitus, Type 1Islets of LangerhansAutoantibodiesBiomarkersGlycated HemoglobinHumansAutoantibodiesBiomarkersGlycated Hemoglobin

Identifiers

PMID35276013
PMCPMC9131426
OpenAlexW4220661255

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.