Evidence map›Paper›PMID 11773116›Full record

ArticleJournal of clinical microbiology2002

Quantitative analysis of mycobacterial and propionibacterial DNA in lymph nodes of Japanese and European patients with sarcoidosis.

Yoshinobu Eishi, Moritaka Suga, Ikuo Ishige, Daisuke Kobayashi, Tetsuo Yamada, Tamiko Takemura, Touichiro Takizawa, Morio Koike, Shoji Kudoh, Ulrich Costabel and 7 more

Abstract read
In one paragraph

Article in Journal of clinical microbiology, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 133 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
133citing papers in PubMed, 3 pooled it
9.5field-weighted citation impact, top 1% 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

133 citing papers in PubMed, 3 syntheses or guidelines pooled it, 439 citations in OpenAlex.

  1. Pooled it
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  8. The Role ofInternational journal of molecular sciences · 2025
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  18. Interleukin-17A plays a key role in pulmonary fibrosis followingExperimental biology and medicine (Maywood, N.J.) · 2023
    Article
  19. Efzofitimod: a novel anti-inflammatory agent for sarcoidosis.Sarcoidosis, vasculitis, and diffuse lung diseases : official journal of WASOG · 2023
    Article
  20. Potential Association ofMicroorganisms · 2023
    Review

73 more citing papers are in PubMed but not listed here.

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

17 authors at 10 institutions in 5 countries.

Yoshinobu EishiDepartment of Human Pathology, School of Medicine, Tokyo Medical and Dental University, Japan. eishi.path@tmd.ac.jp
Moritaka Suga
Ikuo Ishige
Daisuke Kobayashi
Tetsuo Yamada
Tamiko Takemura
Touichiro Takizawa
Morio Koike
Shoji Kudoh
Ulrich Costabel
Josune Guzman
Gianfranco Rizzato
Marcello Gambacorta
Ronald du Bois
Andrew G Nicholson
Om P Sharma
Masayuki Ando
Tokyo Medical and Dental University · JPKumamoto University · JPAzienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda · ITInterstitial Cystitis Association · USJapanese Red Cross Medical Center · JPNippon Medical School · JPRoyal Brompton Hospital · GBRuhrlandklinik · DERuhr University Bochum · DEUniversity of Southern California · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cause(s) of sarcoidosis is unknown. Mycobacterium spp. are suspected in Europe and Propionibacterium spp. are suspected in Japan. The present international collaboration evaluated the possible etiological links between sarcoidosis and the suspected bacterial species. Formalin-fixed and paraffin-embedded sections of biopsy samples of lymph nodes, one from each of 108 patients with sarcoidosis and 65 patients with tuberculosis, together with 86 control samples, were collected from two institutes in Japan and three institutes in Italy, Germany, and England. Genomes of Propionibacterium acnes, Propionibacterium granulosum, Mycobacterium tuberculosis, Mycobacterium avium subsp. paratuberculosis, and Escherichia coli (as the control) were counted by quantitative real-time PCR. Either P. acnes or P. granulosum was found in all but two of the sarcoid samples. M. avium subsp. paratuberculosis was found in no sarcoid sample. M. tuberculosis was found in 0 to 9% of the sarcoid samples but in 65 to 100% of the tuberculosis samples. In sarcoid lymph nodes, the total numbers of genomes of P. acnes or P. granulosum were far more than those of M. tuberculosis. P. acnes or P. granulosum was found in 0 to 60% of the tuberculosis and control samples, but the total numbers of genomes of P. acnes or P. granulosum in such samples were less than those in sarcoid samples. Propionibacterium spp. are more likely than Mycobacteria spp. to be involved in the etiology of sarcoidosis, not only in Japanese but also in European patients with sarcoidosis.

Indexed as

Actinomycetales InfectionsDNA, BacterialEuropeHumansJapanLymph NodesMycobacteriumPolymerase Chain ReactionPropionibacteriumReproducibility of ResultsSarcoidosisSensitivity and SpecificityTaq PolymeraseDNA, BacterialTaq Polymerase

Identifiers

PMID11773116
PMCPMC120089
OpenAlexW2157291255

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.