Evidence map›Paper›PMID 36674562›Full record

ArticleInternational journal of molecular sciences2023

Profiling Microbial Communities in Idiopathic Granulomatous Mastitis.

Seeu Si Ong, Jia Xu, Choon Kiat Sim, Alexis Jiaying Khng, Peh Joo Ho, Philip Kam Weng Kwan, Aarthi Ravikrishnan, Kiat-Tee Benita Tan, Qing Ting Tan, Ern Yu Tan and 8 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
7.3field-weighted citation impact, top 3% 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

20 citing papers in PubMed, 21 citations in OpenAlex.

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  17. Microbiology spectrum · 2024
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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

18 authors at 7 institutions in 1 country.

Seeu Si OngWomen's Health and Genetics, Genome Institute of Singapore, Agency for Science, Technology and Research, Singapore 138672, Singapore.ORCID 0000-0002-2065-4226
Jia XuHuman Development, Singapore Institute for Clinical Sciences, Agency for Science, Technology and Research, Singapore 117609, Singapore.
Choon Kiat SimHuman Development, Singapore Institute for Clinical Sciences, Agency for Science, Technology and Research, Singapore 117609, Singapore.
Alexis Jiaying KhngWomen's Health and Genetics, Genome Institute of Singapore, Agency for Science, Technology and Research, Singapore 138672, Singapore.
Peh Joo HoWomen's Health and Genetics, Genome Institute of Singapore, Agency for Science, Technology and Research, Singapore 138672, Singapore.
Philip Kam Weng KwanDepartment of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228, Singapore.
Aarthi RavikrishnanMetagenomic Technologies and Microbial Systems, Genome Institute of Singapore, Agency for Science, Technology and Research, Singapore 138672, Singapore.
Kiat-Tee Benita TanDivision of Surgical Oncology, National Cancer Centre Singapore, Singapore 169610, Singapore.
Qing Ting TanKK Breast Department, KK Women's and Children's Hospital, Singapore 229899, Singapore.
Ern Yu TanDepartment of General Surgery, Tan Tock Seng Hospital, Singapore 308433, Singapore.
Su-Ming TanDivision of Breast Surgery, Changi General Hospital, Singapore 529889, Singapore.
Thomas Choudary PuttiDepartment of Pathology, National University Health System, Singapore 119228, Singapore.
Swee Ho LimKK Breast Department, KK Women's and Children's Hospital, Singapore 229899, Singapore.
Ee Ling Serene TangDepartment of General Surgery, Tan Tock Seng Hospital, Singapore 308433, Singapore.
Niranjan NagarajanDepartment of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228, Singapore.
Neerja KarnaniHuman Development, Singapore Institute for Clinical Sciences, Agency for Science, Technology and Research, Singapore 117609, Singapore.
Jingmei LiWomen's Health and Genetics, Genome Institute of Singapore, Agency for Science, Technology and Research, Singapore 138672, Singapore.ORCID 0000-0001-8587-7511
Mikael HartmanDepartment of Surgery, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 119228, Singapore.
Agency for Science, Technology and Research · SGKK Women's and Children's Hospital · SGNational University of Singapore · SGChangi General Hospital · SGNational University Health System · SGSingapore General Hospital · SGTan Tock Seng Hospital · SG

Funding

Agency for Science, Technology and Research Not applicableNational University Health System NUHSRO/2020/027/T1/Seed-Aug/11
6 · The paper itself

Abstract

Idiopathic granulomatous mastitis (IGM) is a rare and benign inflammatory breast disease with ambiguous aetiology. Contrastingly, lactational mastitis (LM) is commonly diagnosed in breastfeeding women. To investigate IGM aetiology, we profiled the microbial flora of pus and skin in patients with IGM and LM. A total of 26 patients with IGM and 6 patients with LM were included in the study. The 16S rRNA sequencing libraries were constructed from 16S rRNA gene amplified from total DNA extracted from pus and skin swabs in patients with IGM and LM controls. Constructed libraries were multiplexed and paired-end sequenced on HiSeq4000. Metagenomic analysis was conducted using modified microbiome abundance analysis suite customised R-resource for paired pus and skin samples. Microbiome multivariable association analyses were performed using linear models. A total of 21 IGM and 3 LM paired pus and skin samples underwent metagenomic analysis. Bray−Curtis ecological dissimilarity distance showed dissimilarity across four sample types (IGM pus, IGM skin, LM pus, and LM skin; PERMANOVA, p < 0.001). No characteristic dominant genus was observed across the IGM samples. The IGM pus samples were more diverse than corresponding IGM skin samples (Shannon and Simpson index; Wilcoxon paired signed-rank tests, p = 0.022 and p = 0.07). Corynebacterium kroppenstedtii, reportedly associated with IGM in the literature, was higher in IGM pus samples than paired skin samples (Wilcoxon, p = 0.022). Three other species and nineteen genera were statistically significant in paired IGM pus−skin comparison after antibiotic treatment adjustment and multiple comparisons correction. Microbial profiles are unique between patients with IGM and LM. Inter-patient variability and polymicrobial IGM pus samples cannot implicate specific genus or species as an infectious cause for IGM.

Indexed as

Granulomatous MastitisMicrobiotaFemaleHumansImmunoglobulin MRNA, Ribosomal, 16SSuppurationImmunoglobulin MRNA, Ribosomal, 16S16S rRNACorynebacteriumidiopathic granulomatous mastitisMaAsLin 2metagenomic sequencingmicrobiota

Identifiers

PMID36674562
PMCPMC9863225
OpenAlexW4313572619

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.