Evidence map›Paper›PMID 22998556›Full record

ArticleJournal of proteome research2012

Urinary proteome analysis of irritable bowel syndrome (IBS) symptom subgroups.

Young Ah Goo, Kevin Cain, Monica Jarrett, Lynne Smith, Joachim Voss, Ernie Tolentino, Joyce Tsuji, Yihsuan S Tsai, Alexandre Panchaud, David R Goodlett and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of proteome research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.7field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 33 citations in OpenAlex.

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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

12 authors at 4 institutions in 2 countries.

Young Ah GooDepartment of Biobehavioral Nursing and Health Systems, University of Washington, Seattle, Washington 98195, United States.
Kevin Cain
Monica Jarrett
Lynne Smith
Joachim Voss
Ernie Tolentino
Joyce Tsuji
Yihsuan S Tsai
Alexandre Panchaud
David R Goodlett
Robert J Shulman
Margaret Heitkemper
University of Washington · USNeurobehavioral Systems · USChildren's Nutrition Research Center at Baylor College of Medicine · USNestlé (Switzerland) · CH

Funding

NURSING MANAGEMENT OF IBS--IMPROVING OUTCOMESR01NR004142 · NINR · UNIVERSITY OF WASHINGTON · PI HEITKEMPER, MARGARET MCLEAN · 1996 to 2011
$5.5M
Partnership CoreP30NR004001 · NINR · UNIVERSITY OF WASHINGTON · PI KILLIEN, MARCIA G · 1994 to 2008
$3.7M
Abdominal Symptom Phenotypes: Pathways to New BiomarkersRC2NR011959 · NINR · UNIVERSITY OF WASHINGTON · PI HEITKEMPER, MARGARET MCLEAN, SHULMAN, ROBERT J · 2009 to 2010
$1.9M
NINR NIH HHS P30 NR004001NINR NIH HHS P30 NR04001NINR NIH HHS R01 NR004142NINR NIH HHS RC2 NR011959
6 · The paper itself

Abstract

Irritable bowel syndrome (IBS) is a functional gastrointestinal (GI) disorder characterized by chronic abdominal pain associated with alterations in bowel function. Given the heterogeneity of the symptoms, multiple pathophysiologic factors are suspected to play a role. We classified women with IBS into four subgroups based on distinct symptom profiles. In-depth shotgun proteomic analysis was carried out to profile the urinary proteomes to identify possible proteins associated with these subgroups. First void urine samples with urine creatinine level≥100 mg/dL were used after excluding samples that tested positive for blood. Urine from 10 subjects representing each symptom subgroup was pooled for proteomic analysis. The urine proteome was analyzed by liquid chromatography-tandem mass spectrometry (LC-MS/MS) using a data-independent method known as Precursor Acquisition Independent From Ion Count (PAcIFIC) that allowed extended detectable dynamic range. Differences in protein quantities were determined by peptide spectral counting followed by validation of select proteins with ELISA or a targeted single reaction monitoring (LC-SRM/MS) approach. Four IBS symptom subgroups were selected: (1) Constipation, (2) Diarrhea+Low Pain, (3) Diarrhea+High Pain, and (4) High Pain+High Psychological Distress. A fifth group consisted of Healthy Control subjects. From comparisons of quantitative spectral counting data among the symptom subgroups and controls, a total of 18 proteins that showed quantitative differences in relative abundance and possible physiological relevance to IBS were selected for further investigation. Three of the 18 proteins were chosen for validation by either ELISA or SRM. An elevated expression of gelsolin (GSN) was associated with the high pain groups. Trefoil Factor 3 (TFF3) levels were higher in IBS groups compared to controls. In this study, the IBS patients subclassified by predominant symptoms showed differences in urine proteome levels. Proteins showing distinctive changes are involved in homeostasis of intestinal function and inflammatory response. These findings warrant future studies with larger, independent cohorts to enable more extensive assessment and validation of urinary protein markers as a diagnostic tool in adults with IBS.

Indexed as

Abdominal PainAdultBiomarkersCase-Control StudiesChromatography, LiquidConstipationCreatinineDiarrheaEnzyme-Linked Immunosorbent AssayFemaleGelsolinHumansInflammationIntestinesIrritable Bowel SyndromePeptidesBiomarkersCreatinineGelsolinPeptidesProteomeTFF3 protein, humanTrefoil Factor-3

Identifiers

PMID22998556
PMCPMC3631108
OpenAlexW2087839208

What OpenQuestion holds

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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.