Evidence mapPaperPMID 39420319Full record

ArticleJournal of translational medicine2024

Multi-omics insights into the microbiota-gut-brain axis and cognitive improvement post-bariatric surgery.

Qiaoyuan Xiang, Minhua Yu, Qi Cai, Mengjie Hu, Bo Rao, Xin Liang, Zhenxing Liu, Yu Xie, Kuan Cen, Renwei Zhang and 2 more

Abstract read
In one paragraph

Article in Journal of translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
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

4 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Review
  4. Review
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.

Qiaoyuan Xiang *Dapartment of Neurology, Zhongnan Hospital of Wuhan University, No.169 Donghu Street, Wuhan, Hubei, 430000, China.
Minhua Yu *Department of Radiology, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Qi CaiDapartment of Neurology, Zhongnan Hospital of Wuhan University, No.169 Donghu Street, Wuhan, Hubei, 430000, China.
Mengjie HuDepartment of Hepatobiliary, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Bo RaoDepartment of Radiology, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China.
Xin LiangDapartment of Neurology, Zhongnan Hospital of Wuhan University, No.169 Donghu Street, Wuhan, Hubei, 430000, China.
Zhenxing LiuDepartment of Neurology, Yiling Hospital of Yichang City, Yichang, Hubei, China.
Yu XieDapartment of Neurology, Zhongnan Hospital of Wuhan University, No.169 Donghu Street, Wuhan, Hubei, 430000, China.
Kuan CenDapartment of Neurology, Zhongnan Hospital of Wuhan University, No.169 Donghu Street, Wuhan, Hubei, 430000, China.
Renwei ZhangDapartment of Neurology, Zhongnan Hospital of Wuhan University, No.169 Donghu Street, Wuhan, Hubei, 430000, China.
Haibo XuDepartment of Radiology, Zhongnan Hospital of Wuhan University, Wuhan, Hubei, China. xuhaibo@whu.edu.cn.
Yumin LiuDapartment of Neurology, Zhongnan Hospital of Wuhan University, No.169 Donghu Street, Wuhan, Hubei, 430000, China. wb001792@whu.edu.cn.ORCID 0000-0002-6446-4731

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough numerous studies have shown that bariatric surgery results in sustained weight loss and modifications in gut microbiota composition and cognitive function, the exact underlying mechanisms are unclear. This study aimed to investigate the effects of bariatric surgery on cognitive function through the microbiota-gut-brain axis (MGBA).

methodsDemographic data, serum samples, fecal samples, cognitive assessment scales, and resting-state functional connectivity magnetic resonance imaging (rs-fMRI) scans were obtained from 39 obese patients before and after (6 months) laparoscopic sleeve gastrectomy (LSG). PCA analysis, OPLS-DA analysis, and permutation tests were used to conduct fecal 16 S microbiota profiling, serum metabolomics, and neuroimaging analyses, and a bariatric surgery-specific rs-fMRI brain functional connectivity network was constructed. Spearman correlation analysis and Co-inertia analysis were employed to correlate significant alterations in cognitive assessment scales and resting-state functional connectivity difference networks with differential serum metabolites and 16 S microbiota data to identify key gut microbiota and serum metabolic factors.

resultsLSG significantly reduced the weight of obese patients, with reductions of up to 28%. Furthermore, cognitive assessment scale measurements revealed that LSG enhanced cognitive functions, including memory (HVLT, p = 0.000) and executive function (SCWT, p = 0.008). Also, LSG significantly altered gut microbiota composition (p = 0.001), with increased microbial abundance and diversity (p < 0.05). Moreover, serum metabolite levels were significantly altered, revealing intergroup differences in 229 metabolites mapped to 72 metabolic pathways (p < 0.05, VIP > 1). Spearman correlation analysis among cognitive assessment scales, gut microbiota species, and serum metabolites revealed correlations with 68 gut microbiota species and 138 serum metabolites (p < 0.05). Furthermore, pairwise correlations were detected between gut microbiota and serum metabolites (p < 0.05). Functional neuroimaging analysis revealed that LSG increased functional connectivity in cognitive-related frontotemporal networks (FPN, p < 0.01). Additionally, normalization of the default mode network (DMN) and salience network (SN) connectivity was observed after LSG (p < 0.001). Further canonical correlation and correlation analysis suggested that the cognitive-related brain network changes induced by LSG were associated with key gut microbiota species (Akkermansia, Blautia, Collinsella, Phascolarctobacterium, and Ruminococcus, p < 0.05) and neuroactive metabolites (Glycine, L-Serine, DL-Dopa, SM (d18:1/24:1(15Z), p < 0.05).

conclusionThese findings indicate the pathophysiological role of the microbiota-gut-brain axis in enhancing cognitive function after bariatric surgery, and the study provides a basis for clinical dietary adjustments, probiotic supplementation, and guidance for bariatric surgery, but further research is still needed.

trial registrationChinese Clinical Trial Registry, ChiCTR2100049403. Registered 02 August 2021, https://www.chictr.org.cn/ .

Indexed as

Bariatric SurgeryBrain-Gut AxisCognitionGastrointestinal MicrobiomeMagnetic Resonance ImagingAdultBrainFecesFemaleHumansMaleMetabolomicsMiddle AgedMultiomicsObesityBariatric surgeryCognitive functionFunctional connectivityMetabolitesMicrobiotaMicrobiota-gut-brain axisMulti-omicsNeuroimaging

Identifiers

PMID39420319
PMCPMC11484437

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.