Evidence map›Paper›PMID 39439976›Full record

ArticleRheumatology and immunology research2024

Fibroblast activation protein inhibitor PET/CT as an emerging diagnostic modality in interstitial lung disease and other fibrotic conditions.

Mihai Tudor Albu, Alexandru-Emil Matei, Jörg H W Distler, Frederik L Giesel, Yuriko Mori

Abstract read
In one paragraph

Article in Rheumatology and immunology research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. [Scientific reports · 2026
    Article
  3. Review
  4. Article
  5. EJNMMI research · 2025
    Article
  6. Article
  7. Prognostic value of [Scientific reports · 2025
    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

5 authors.

Mihai Tudor AlbuDepartment of Rheumatology, University Hospital Düsseldorf, Medical Faculty of Heinrich-Heine University; Düsseldorf, Germany.
Alexandru-Emil MateiDepartment of Rheumatology, University Hospital Düsseldorf, Medical Faculty of Heinrich-Heine University; Düsseldorf, Germany.
Jörg H W DistlerDepartment of Rheumatology, University Hospital Düsseldorf, Medical Faculty of Heinrich-Heine University; Düsseldorf, Germany.
Frederik L GieselDepartment of Nuclear Medicine, University Hospital Düsseldorf, Medical Faculty of Heinrich-Heine University; Düsseldorf, Germany.
Yuriko MoriDepartment of Nuclear Medicine, University Hospital Düsseldorf, Medical Faculty of Heinrich-Heine University; Düsseldorf, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interstitial lung diseases (ILD) encompass a wide range of disorders characterized by alveolar inflammation and fibrotic tissue remodeling, marked by significant morbidity and mortality. Systemic sclerosis (SSc), among other connective tissue diseases, is a frequent cause of ILD. Assessment of pulmonary fibrosis is frequently constrained by the delayed manifestations of profibrotic activation of fibroblasts, which results in late macroscopic alterations detectable by standard imaging techniques such as computed tomography (CT) and magnetic resonance imaging (MRI) scans. 68Ga-labeled fibroblast activation protein inhibitors (68Ga-FAPI [fibroblast activation protein inhibitor]) are novel radionuclides used in the selective positron emission tomography/computed tomography (PET/CT) detection of profibrotic fibroblasts, a key player in fibrotic tissue remodeling. Application of 68Ga-FAPI in different target organs undergoing fibrosis, such as lung and heart, highlights its efficacy in detecting ongoing fibrotic processes, since FAPI tracer uptake has been correlated with clinical disease progression markers in SSc-ILD. This feature could enable physicians to detect subclinical fibrotic activity and tailor an individualised therapy plan on a case by case basis. The use of 68Ga-FAPI in ILD and other fibrotic conditions may emerge as a novel tool in future clinical practice for both activity monitoring and treatment optimisation. Other tracers tested in ILD of different etiologies have shown promising results and may in future also be considered for potential application in SSc-ILD.

Indexed as

fibroblastsfibrosisinterstitial lung diseasessystemic sclerosis

Identifiers

PMID39439976
PMCPMC11492823

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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.