Evidence map›Paper›PMID 32358162›Full record

ArticleThe Journal of rheumatology2021

Phenylalanine Is a Novel Marker for Radiographic Knee Osteoarthritis Progression: The MOST Study.

Guangju Zhai, Xianbang Sun, Edward W Randell, Ming Liu, Na Wang, Irina Tolstykh, Proton Rahman, James Torner, Cora E Lewis, Michael C Nevitt and 3 more

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in The Journal of rheumatology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 2 pooled it
1.6field-weighted citation impact, top 17% 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, 2 syntheses or guidelines pooled it, 24 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

13 authors at 6 institutions in 3 countries.

Guangju ZhaiG. Zhai, PhD, M. Liu, MSc, Discipline of Genetics, Faculty of Medicine, Memorial University of Newfoundland, St. John's, Newfoundland, Canada; guangju.zhai@med.mun.ca.ORCID 0000-0002-7263-0605
Xianbang SunX. Sun, MS, Department of Rheumatology, Boston University School of Medicine, Boston, USA.
Edward W RandellE. Randell, PhD, Division of Laboratory Medicine, Faculty of Medicine, Memorial University of Newfoundland, St. John's, Newfoundland, Canada.
Ming LiuG. Zhai, PhD, M. Liu, MSc, Discipline of Genetics, Faculty of Medicine, Memorial University of Newfoundland, St. John's, Newfoundland, Canada.
Na WangN. Wang, PhD, Biostatistics and Epidemiology Data Analytics Center, Boston University School of Public Health, Boston, USA.
Irina TolstykhI. Tolstykh, MS, M.C. Nevitt, PhD, MPH, Epidemiology and Biostatistics, University of California, San Francisco, USA.
Proton RahmanP. Rahman, MD, Discipline of Medicine, Faculty of Medicine, Memorial University of Newfoundland, St. John's, Newfoundland, Canada.
James TornerJ. Torner, PhD, Department of Epidemiology, University of Iowa, Iowa City, Iowa, USA.
Cora E LewisC.E. Lewis, MD, Department of Epidemiology, University of Alabama, Birmingham, USA.
Michael C NevittI. Tolstykh, MS, M.C. Nevitt, PhD, MPH, Epidemiology and Biostatistics, University of California, San Francisco, USA.
Ali GuermaziA. Guermazi, MD, PhD, F. Roemer, MD, Department of Radiology, Boston University School of Medicine, Boston, USA.
Frank RoemerA. Guermazi, MD, PhD, F. Roemer, MD, Department of Radiology, Boston University School of Medicine, Boston, USA.
David T FelsonD.T. Felson, MD, MPH, Department of Rheumatology, Boston University School of Medicine, Boston, USA, and NIHR Manchester Biomedical Research Centre, Manchester Academic Health Science Centre, Manchester University NHS Foundation Trust, Manchester, UK.
Boston University · USMemorial University of Newfoundland · CAUniversity of California, San Francisco · USManchester Academic Health Science Centre · GBUniversity of Alabama at Birmingham · USUniversity of Iowa · US

Funding

Multicenter Osteoarthritis Study (MOST) Second RenewalU01AG019069 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI NEVITT, MICHAEL C · 2001 to 2020
$21.7M
Multicenter Osteoarthritis Study (MOST) Second Renewal: Iowa Clinical CenterU01AG018832 · NIA · UNIVERSITY OF IOWA · PI SEGAL, NEIL A, TORNER, JAMES C · 2001 to 2020
$14.1M
Multicenter Osteoarthritis Study (MOST) Second Renewal - Boston UniversityU01AG018820 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI FELSON, DAVID TOBIN · 2001 to 2019
$13.6M
Multicenter Osteoarthritis Study (MOST) Second Renewal - UAB Clinical CenterU01AG018947 · NIA · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LEWIS, CORA E · 2001 to 2020
$13.2M
Research and Evaluation Support Core Unit (RESCU Core)P30AR072571 · NIAMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI TUHINA NEOGI · 2019 to 2026
$6.9M
NIAMS NIH HHS P30 AR072571NIA NIH HHS U01 AG018820NIA NIH HHS U01 AG018832NIA NIH HHS U01 AG018947NIA NIH HHS U01 AG019069
6 · The paper itself

Abstract

objectiveTo identify plasma markers associated with an increased risk of radiographic knee osteoarthritis(OA) progression using a metabolomics approach.

methodsStudy participants were from the Multicenter Osteoarthritis Study (MOST) and were categorized into 2 groups based on the presence of baseline radiographic OA. Subjects in group 1 had unilateral knee OA and subjects in group 2 had bilateral knee OA. Progression was defined as a half-grade or greater worsening in joint space width at 30-month follow-up. For group 1, a participant progressed when their OA knee showed radiographic progression and the contralateral knee developed OA; for group 2, a participant progressed when both knees with OA showed radiographic progression. Metabolomic profiling was performed on plasma samples collected at baseline and logistic regression was performed to test the association between each metabolite and knee OA progression after adjustment for age, sex, BMI, and clinic site. Significance was defined as

resultsThere were 234 progressors (57 in group 1 and 177 in group 2) and 322 nonprogressors (206 in group 1 and 116 in group 2) included in the analyses. Among 157 metabolites studied, we found that odds of progression were 1.46 times higher per SD increase of phenylalanine level (95% CI 1.20-1.77,

conclusionOur data suggest that phenylalanine might be a novel plasma marker for higher risk of bilateral radiographic knee OA progression in women.

Indexed as

Osteoarthritis, KneeDisease ProgressionFemaleHumansKnee JointMalePhenylalanineRadiographyPhenylalanineknee osteoarthritismetabolomicsplasma biomarkersprogressionradiograph

Identifiers

PMID32358162
PMCPMC8039838
OpenAlexW3021047744

What OpenQuestion holds

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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.