Evidence map›Paper›PMID 30620405›Full record

ArticlePharmacotherapy2019

Effects of Atypical Antipsychotic Treatment and Resistant Starch Supplementation on Gut Microbiome Composition in a Cohort of Patients with Bipolar Disorder or Schizophrenia.

Stephanie A Flowers, Nielson T Baxter, Kristen M Ward, A Zarina Kraal, Melvin G McInnis, Thomas M Schmidt, Vicki L Ellingrod

Abstract read
In one paragraph

Article in Pharmacotherapy, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 4 pooled it
7.6field-weighted citation impact, top 2% 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

40 citing papers in PubMed, 4 syntheses or guidelines pooled it, 100 citations in OpenAlex.

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  17. Extracellular Vesicles in Mental Disorders: A State-of-art Review.International journal of biological sciences · 2023
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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

7 authors at 2 institutions in 1 country.

Stephanie A FlowersDepartment of Pharmacy Practice, University of Illinois at Chicago, Chicago, Illinois.ORCID 0000-0001-5149-9444
Nielson T BaxterDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan.
Kristen M WardDepartment of Clinical Pharmacy, University of Michigan, Ann Arbor, Michigan.
A Zarina KraalDepartment of Clinical Pharmacy, University of Michigan, Ann Arbor, Michigan.
Melvin G McInnisDepartment of Psychiatry, University of Michigan, Ann Arbor, Michigan.
Thomas M SchmidtDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan.
Vicki L EllingrodDepartment of Clinical Pharmacy, University of Michigan, Ann Arbor, Michigan.
University of Michigan · USUniversity of Illinois Chicago · US

Funding

Michigan Institute for Clinical and Health Research (MICHR)UL1TR002240 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LUMENG, JULIE C, MASHOUR, GEORGE ALEXANDER · 2017 to 2022
$54.9M
Folate Pharmacogenomics and Risk of Atypical Antipsychtoic Metabolic Side EffectsR01MH082784 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELLINGROD, VICKI L · 2008 to 2017
$4.0M
Development, Implementation and AssessMent of Novel Training in Domain-based Competencies (DIAMOND)U01TR002013 · NCATS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELLINGROD, VICKI L, JONES, CAROLYNN THOMAS · 2017 to 2019
$2.3M
NCATS NIH HHS U01 TR002013NCATS NIH HHS UL1 TR002240NIH HHS UL1TR002240NIMH NIH HHS R01 MH082784NIMH NIH HHS R01MH082784
6 · The paper itself

Abstract

STUDY

objectivePrevious studies identified shifts in gut microbiota associated with atypical antipsychotic (AAP) treatment that may link AAPs to metabolic burden. Dietary prebiotics such as resistant starch may be beneficial in obesity and glucose regulation, but little is known mechanistically about their ability to modify gut microbiota in AAP-treated individuals. This investigation was undertaken to delineate mechanistically the effects of AAP treatment and resistant starch supplementation on gut microbiota in a psychiatric population.

designCross-sectional cohort study.

settingThe study was performed in an outpatient setting. PATIENTS: A total of 37 adults with a diagnosis of bipolar disorder or schizophrenia who were treated with an AAP (clozapine, olanzapine, risperidone, quetiapine, or ziprasidone [21 patients]) or lithium and/or lamotrigine (16 patients) for at least 6 months.

interventionPatients in the AAP group received raw unmodified potato starch (resistant starch) daily for 14 days. MEASUREMENTS AND MAIN

resultsOf the 37 patients, the mean ± SD age was 52.2 ± 12.5 years, and 57% were male. The primary outcome was gut microbiome DNA composition. Microbiome DNA obtained from stool samples from all patients was subject to 16S ribosomal RNA (rRNA) gene sequencing before and during resistant starch supplementation. Inter- and intragroup microbial diversity measures were performed by permutational multivariate analysis of variance and the Inverse Simpson Diversity Index, respectively. Differentially abundant organisms were detected by using linear discriminant analysis effect size. Although no significant difference in overall microbiota composition was detected at baseline between AAP users and nonusers, non-AAP users showed increased fractional representation of Alistipes. AAP-treated women exhibited decreased diversity compared with non-AAP-treated women. Although the microbiome of AAP-treated patients varied with resistant starch administration, an increased abundance of the Actinobacteria phylum was observed.

conclusionThese data suggest that AAP treatment is associated with measurable differences in gut microbiota, particularly in female AAP-treated patients in whom reduced species richness was observed. Additionally, variable microbiome responses to resistant starch supplementation were seen, with a significant increase in starch degraders.

Indexed as

PrebioticsAntipsychotic AgentsBipolar DisorderCohort StudiesCross-Sectional StudiesFemaleGastrointestinal MicrobiomeHumansMaleMiddle AgedRNA, Ribosomal, 16SSchizophreniaSurveys and QuestionnairesAntipsychotic AgentsPrebioticsRNA, Ribosomal, 16Satypical antipsychoticbipolar disordermicrobiomeresistant starchschizophrenia

Identifiers

PMID30620405
PMCPMC6386623
OpenAlexW2910111650

What OpenQuestion holds

Textmetadata
LicenceTDM
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.