Evidence map›Paper›PMID 37848575›Full record

ArticleScientific reports2023

Outcomes and prognosis of progressive pulmonary fibrosis in patients with antineutrophil cytoplasmic antibody-positive interstitial lung disease.

Susumu Sakamoto, Aika Suzuki, Sakae Homma, Yusuke Usui, Hiroshige Shimizu, Muneyuki Sekiya, Shion Miyoshi, Yasuhiko Nakamura, Naohisa Urabe, Takuma Isshiki and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
5.4field-weighted citation impact, top 4% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 21 citations in OpenAlex.

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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

12 authors at 2 institutions in 1 country.

Susumu SakamotoDivision of Respiratory Medicine, Toho University Omori Medical Center, 6-11-1, Ota-Ku Omori Nisi, Tokyo, 143-8541, Japan. susumu1029@med.toho-u.ac.jp.
Aika SuzukiDivision of Respiratory Medicine, Toho University Omori Medical Center, 6-11-1, Ota-Ku Omori Nisi, Tokyo, 143-8541, Japan.
Sakae HommaDivision of Respiratory Medicine, Toho University Omori Medical Center, 6-11-1, Ota-Ku Omori Nisi, Tokyo, 143-8541, Japan.
Yusuke UsuiDivision of Respiratory Medicine, Toho University Omori Medical Center, 6-11-1, Ota-Ku Omori Nisi, Tokyo, 143-8541, Japan.
Hiroshige ShimizuDivision of Respiratory Medicine, Toho University Omori Medical Center, 6-11-1, Ota-Ku Omori Nisi, Tokyo, 143-8541, Japan.
Muneyuki SekiyaDivision of Respiratory Medicine, Toho University Omori Medical Center, 6-11-1, Ota-Ku Omori Nisi, Tokyo, 143-8541, Japan.
Shion MiyoshiDivision of Respiratory Medicine, Toho University Omori Medical Center, 6-11-1, Ota-Ku Omori Nisi, Tokyo, 143-8541, Japan.
Yasuhiko NakamuraDivision of Respiratory Medicine, Toho University Omori Medical Center, 6-11-1, Ota-Ku Omori Nisi, Tokyo, 143-8541, Japan.
Naohisa UrabeDivision of Respiratory Medicine, Toho University Omori Medical Center, 6-11-1, Ota-Ku Omori Nisi, Tokyo, 143-8541, Japan.
Takuma IsshikiDivision of Respiratory Medicine, Toho University Omori Medical Center, 6-11-1, Ota-Ku Omori Nisi, Tokyo, 143-8541, Japan.
Atsuko KurosakiDepartment of Diagnostic Radiology, Fukujuji Hospital, Kiyose, Tokyo, Japan.
Kazuma KishiDivision of Respiratory Medicine, Toho University Omori Medical Center, 6-11-1, Ota-Ku Omori Nisi, Tokyo, 143-8541, Japan.
Toho University · JPFukujuji Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Approximately one-third of fibrosing interstitial lung diseases exhibit progressive pulmonary fibrosis (PPF), a clinicopathological condition distinct yet resembling idiopathic pulmonary fibrosis (IPF). PPF in ANCA-positive ILD (ANCA-ILD) is poorly documented. To clarify incidence, predictors of PPF in ANCA-ILD, and their prognostic impact, 56 patients with ANCA-ILD were followed for ≥ 1 year (April 2004 to April 2021). PPF was defined per ATS/ERS/JRS/ALAT PPF 2022 guideline. We compared PPF and non-PPF in 38 patients with pulmonary function tests and ≥ 1 year follow up. ANCA-ILD (19 male, 19 female; mean age 72 years) comprised 21 patients with microscopic polyangiitis ILD (MPA-ILD) and 17 with ANCA-positive IP without systemic vasculitis (ANCA-IP). PPF occurred in 15/38 (39.5%) overall, and 27% of patients with MPA-ILD and 53% with ANCA-IP. Patient characteristics did not differ between PPF and non-PPF, however, the survival was significantly worse in patients with PPF than those with non-PPF. On multivariate regression analysis, higher age, higher serum SP-D level, and lower baseline %FVC were associated with PPF. In ANCA-ILD, 39.5% of patients demonstrated PPF, which is associated with increased mortality. Predictors of PPF were older age, higher SP-D, and lower baseline %FVC.

Indexed as

Idiopathic Pulmonary FibrosisLung Diseases, InterstitialMicroscopic PolyangiitisAgedAntibodies, Antineutrophil CytoplasmicFemaleHumansMalePrognosisPulmonary Surfactant-Associated Protein DRetrospective StudiesAntibodies, Antineutrophil CytoplasmicPulmonary Surfactant-Associated Protein D

Identifiers

PMID37848575
PMCPMC10582016
OpenAlexW4387703250

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.