Evidence map›Paper›PMID 36177295›Full record

ArticleThe Lancet. Rheumatology2022

Prediction models for the risk of total knee replacement: development and validation using data from multicentre cohort studies.

Qiang Liu, Hongling Chu, Michael P LaValley, David J Hunter, Hua Zhang, Liyuan Tao, Siyan Zhan, Jianhao Lin, Yuqing Zhang

Open access · greenAbstract read
In one paragraph

Article in The Lancet. Rheumatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
7.2field-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

27 citing papers in PubMed, 37 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

9 authors at 3 institutions in 2 countries.

Qiang LiuPeking University People's Hospital, Arthritis Clinic and Research Center, Beijing, China; Massachusetts General Hospital, Harvard Medical School, Division of Rheumatology, Immunology and Allergy, Boston, MA, USA.
Hongling ChuPeking University Third Hospital, Research Center of Clinical Epidemiology, Beijing, China.
Michael P LaValleyBoston University School of Public Health, Boston, MA, USA.
David J HunterInstitute of Bone and Joint Research, The Kolling Institute, Sydney Medical School, The University of Sydney, Sydney, NSW, Australia; Rheumatology Department, Royal North Shore Hospital, Sydney, NSW, Australia.
Hua ZhangPeking University Third Hospital, Research Center of Clinical Epidemiology, Beijing, China.
Liyuan TaoPeking University Third Hospital, Research Center of Clinical Epidemiology, Beijing, China.
Siyan ZhanPeking University Third Hospital, Research Center of Clinical Epidemiology, Beijing, China; Peking University Health Science Center, School of Public Health, Beijing, China.
Jianhao LinPeking University People's Hospital, Arthritis Clinic and Research Center, Beijing, China.
Yuqing ZhangMassachusetts General Hospital, Harvard Medical School, Division of Rheumatology, Immunology and Allergy, Boston, MA, USA.
Peking University Third Hospital · CNBoston University · USPeking University · CN

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
NIA NIH HHS U01 AG018820NIA NIH HHS U01 AG018832NIA NIH HHS U01 AG018947NIA NIH HHS U01 AG019069
6 · The paper itself

Abstract

Background: Few prognostic prediction models for total knee replacement are available, and the role of radiographic findings in predicting its use remains unclear. We aimed to develop and validate predictive models for total knee replacement and to assess whether adding radiographic findings improves predictive performance. Methods: We identified participants with recent knee pain (in the past 3 months) in the Multicenter Osteoarthritis Study (MOST) and the Osteoarthritis Initiative (OAI). The baseline visits of MOST were initiated in 2003 and of OAI were initiated in 2004. We developed two predictive models for the risk of total knee replacement within 60 months of follow-up by fitting Cox proportional hazard models among participants in MOST. The first model included sociodemographic and anthropometric factors, medical history, and clinical measures (referred to as the clinical model). The second model added radiographic findings into the predictive model (the radiographic model). We evaluated each model's discrimination and calibration performance and assessed the incremental value of radiographic findings using both category-free net reclassification improvement (NRI) and integrated discrimination improvement (IDI). We tuned the models and externally validated them among participants in OAI. Findings: We included 2658 participants from MOST (mean age 62·4 years [SD 8·1], 1646 [61·9%] women) in the training dataset and 4060 participants from OAI (mean age 60·9 years [9·1], 2379 [58·6%] women) in the validation dataset. 290 (10·9%) participants in the training dataset and 174 (4·3%) in the validation dataset had total knee replacement. The retained predictive variables included in the clinical model were age, sex, race, history of knee arthroscopy, frequent knee pain, current use of analgesics, current use of glucosamine, body-mass index, and Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) pain score, and the most predictive factors were age, race, and WOMAC pain score. The retained predictive variables in the radiographic model were age, sex, race, frequent knee pain, current use of analgesics, WOMAC pain score, and Kellgren-Lawrence grade, and the most predictive factors were Kellgren-Lawrence grade, race, and age. The C-statistic was 0·79 (95% CI 0·76-0·81) for the clinical model and 0·87 (0·85-0·99) for the radiographic model in the training dataset. The calibration slope was 0·95 (95% CI 0·86-1·05) and 0·96 (0·87-1·04), respectively. Adding radiograph findings significantly improved predictive performance with an NRI of 0·43 (95% CI 0·38-0·50) and IDI of 0·14 (95% CI: 0·10-0·18). Both models, with tuned coefficients, showed a good predictive performance among participants in the validation dataset. Interpretation: The risk of total knee replacement can be predicted based on common risk factors with good discrimination and calibration. Additionally, adding radiographic findings of knee osteoarthritis into the model substantially improves its predictive performance. Funding: National Natural Science Foundation of China, National Key Research and Development Program, and Beijing Municipal Science & Technology Commission.

Identifiers

PMID36177295
PMCPMC9517949
OpenAlexW4211252799

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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.