Evidence map›Paper›PMID 36341382›Full record

ArticleFrontiers in immunology2022

Alterations of the gut microbiota in patients with immunoglobulin light chain amyloidosis.

Jipeng Yan, Jin Zhao, Xiaoxuan Ning, Yunlong Qin, Yan Xing, Yuwei Wang, Qing Jia, Boyong Huang, Rui Ma, Changhui Lei and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 41% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

15 authors at 3 institutions in 1 country.

Jipeng YanDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Jin ZhaoDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Xiaoxuan NingDepartment of Geriatrics, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Yunlong QinDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Yan XingDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Yuwei WangDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Qing JiaDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Boyong HuangDepartment of Geriatrics, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Rui MaDepartment of Geriatrics, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Changhui LeiXijing Hypertrophic Cardiomyopathy Center, Department of Ultrasound, Xijing Hospital, Xi'an, China.
Meilan ZhouDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Zixian YuDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Yumeng ZhangDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Wei-Feng GuoSchool of Electrical Engineering, Zhengzhou University, Zhengzhou, China.
Shiren SunDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Xijing Hospital · CNAir Force Medical University · CNZhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Emerging evidence revealed that gut microbial dysbiosis is implicated in the development of plasma cell dyscrasias and amyloid deposition diseases, but no data are available on the relationship between gut microbiota and immunoglobulin light chain (AL) amyloidosis. Methods: To characterize the gut microbiota in patients with AL amyloidosis, we collected fecal samples from patients with AL amyloidosis (n=27) and age-, gender-, and BMI-matched healthy controls (n=27), and conducted 16S rRNA MiSeq sequencing and amplicon sequence variants (ASV)-based analysis. Results: There were significant differences in gut microbial communities between the two groups. At the phylum level, the abundance of Conclusions: For the first time, we demonstrated the alterations of gut microbiota in AL amyloidosis and successfully established and validated the microbial-based diagnostic model, which boosted more studies about microbe-based strategies for diagnosis and treatment in patients with AL amyloidosis in the future.

Indexed as

Gastrointestinal MicrobiomeImmunoglobulin Light-chain AmyloidosisBiomarkersDysbiosisFecesHumansRNA, Ribosomal, 16SBiomarkersRNA, Ribosomal, 16SAL amyloidosisamyloidgut dysbiosisgut microbiotaimmunoglobulin light chain amyloidosis

Identifiers

PMID36341382
PMCPMC9628213
OpenAlexW4306845833

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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.