Prognostic model to predict the incidence of radiographic knee osteoarthritis

被引:3
作者
Paz-Gonzalez, Rocio [1 ]
Balboa-Barreiro, Vanesa [1 ]
Lourido, Lucia [1 ]
Calamia, Valentina [1 ]
Fernandez-Puente, Patricia [2 ]
Oreiro, Natividad [1 ,3 ]
Ruiz-Romero, Cristina [1 ,3 ]
Blanco, Francisco J. [1 ,2 ]
机构
[1] INIBIC Hosp Univ A Coruna, Grp Invest Reumatol GIR, SERGAS, La Coruna 15006, Spain
[2] Univ A Coruna, Ctr Interdisciplinar Quim Biol CICA, Dept Fisioterapia & Med, Grp Reumatol & Salud, La Coruna, Spain
[3] Ctr Invest Biomed Red Bioingn Biomat & Nanomed CIB, La Coruna, Spain
基金
美国国家卫生研究院;
关键词
Knee Osteoarthritis; Incidence; Outcome Assessment; Health Care; Chondrocytes; Osteoarthritis; SYNOVIAL-FLUID; BIOMARKERS; CARTILAGE; DIAGNOSIS; SERUM;
D O I
10.1136/ard-2023-225090
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
ObjectiveEarly diagnosis of knee osteoarthritis (KOA) in asymptomatic stages is essential for the timely management of patients using preventative strategies. We develop and validate a prognostic model useful for predicting the incidence of radiographic KOA (rKOA) in non-radiographic osteoarthritic subjects and stratify individuals at high risk of developing the disease.MethodsSubjects without radiographic signs of KOA according to the Kellgren and Lawrence (KL) classification scale (KL=0 in both knees) were enrolled in the OA initiative (OAI) cohort and the Prospective Cohort of A Coruna (PROCOAC). Prognostic models were developed to predict rKOA incidence during a 96-month follow-up period among OAI participants based on clinical variables and serum levels of the candidate protein biomarkers APOA1, APOA4, ZA2G and A2AP. The predictive capability of the biomarkers was assessed based on area under the curve (AUC), and internal validation was performed to correct for overfitting. A nomogram was plotted based on the regression parameters. Model performance was externally validated in the PROCOAC.Results282 participants from the OAI were included in the development dataset. The model built with demographic, anthropometric and clinical data (age, sex, body mass index and WOMAC pain score) showed an AUC=0.702 for predicting rKOA incidence during the follow-up. The inclusion of ZA2G, A2AP and APOA1 data significantly improved the model's sensitivity and predictive performance (AUC=0.831). The simplest model, including only clinical covariates and ZA2G and A2AP serum levels, achieved an AUC=0.826. Both models were internally cross-validated. Predictive performance was externally validated in an independent dataset of 100 individuals from the PROCOAC (AUC=0.713).ConclusionA novel prognostic model based on common clinical variables and protein biomarkers was developed and externally validated to predict rKOA incidence over a 96-month period in individuals without any radiographic signs of disease. The resulting nomogram is a useful tool for stratifying high-risk populations and could potentially lead to personalised medicine strategies for treating OA.
引用
收藏
页码:661 / 668
页数:8
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