1. In silico validation of the Autoinflammatory Disease Damage Index
- Author
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Eric Hachulla, Michael Hofer, Susanne M. Benseler, Nienke M. Ter Haar, Giovanna Fabio, Annette Jansson, Efimia Papadopoulou-Alataki, Antonella Insalaco, Hal M Hoffman, Pavla Dolezalova, Grant S. Schulert, Isabelle Koné-Paut, Karyl S. Barron, Troels Herlin, Adriana Almeida de Jesus, Alexis Virgil Cochino, Marco Cattalini, Ronald M. Laxer, Gayane Amaryan, Jordi Anton, Anna Kozlova, Maria Trachana, Véronique Hentgen, Jasmin B Kuemmerle-Deschner, Susan Nielsen, Tilmann Kallinich, Karen L. Durrant, Erkan Demirkaya, Romina Gallizzi, Amanda K. Ombrello, Seza Ozen, Alberto Martini, Fatma Dedeoglu, Ricardo Russo, Fabrizio De Benedetti, Joost Frenkel, Pierre Quartier, Henk F. van Stel, Luca Cantarini, Kim V. Annink, Donato Rigante, Helen J. Lachmann, Marco Gattorno, Yosef Uziel, Anna Simon, Irina Nikishina, Raphaela Goldbach-Mansky, Sulaiman M. Al-Mayouf, Amber Laetitia Justine Van Delft, Paul A. Brogan, and Angelo Ravelli
- Subjects
0301 basic medicine ,Genetics and Molecular Biology (all) ,familial Mediterranean fever, fever syndromes, inflammation, Adolescent, Adult, Child, Computer Simulation, Cryopyrin-Associated Periodic Syndromes, Familial Mediterranean Fever, Hereditary Autoinflammatory Diseases, Humans, Mevalonate Kinase Deficiency, Observer Variation, Registries, Reproducibility of Results, Young Adult, Severity of Illness index ,Intraclass correlation ,Familial Mediterranean fever ,Disease ,Biochemistry ,Severity of Illness Index ,fever syndromes ,0302 clinical medicine ,familial Mediterranean fever ,Medicine ,Immunology and Allergy ,Registries ,Child ,Observer Variation ,inflammation ,Rheumatology ,Immunology ,Biochemistry, Genetics and Molecular Biology (all) ,Familial Mediterranean Fever ,Settore MED/38 - PEDIATRIA GENERALE E SPECIALISTICA ,Autoinflammation ,Inflammatory diseases Radboud Institute for Molecular Life Sciences [Radboudumc 5] ,Adult ,medicine.medical_specialty ,Adolescent ,General Biochemistry, Genetics and Molecular Biology ,Article ,03 medical and health sciences ,Young Adult ,Cronbach's alpha ,Internal medicine ,Severity of illness ,Humans ,Computer Simulation ,Face validity ,030203 arthritis & rheumatology ,business.industry ,Biochemistry, Genetics and Molecular Biology(all) ,Hereditary Autoinflammatory Diseases ,Construct validity ,Reproducibility of Results ,medicine.disease ,Cryopyrin-Associated Periodic Syndromes ,030104 developmental biology ,Mevalonate Kinase Deficiency ,business ,Genetics and Molecular Biology(all) - Abstract
IntroductionAutoinflammatory diseases can cause irreversible tissue damage due to systemic inflammation. Recently, the Autoinflammatory Disease Damage Index (ADDI) was developed. The ADDI is the first instrument to quantify damage in familial Mediterranean fever, cryopyrin-associated periodic syndromes, mevalonate kinase deficiency and tumour necrosis factor receptor-associated periodic syndrome. The aim of this study was to validate this tool for its intended use in a clinical/research setting.MethodsThe ADDI was scored on paper clinical cases by at least three physicians per case, independently of each other. Face and content validity were assessed by requesting comments on the ADDI. Reliability was tested by calculating the intraclass correlation coefficient (ICC) using an ‘observer-nested-within-subject’ design. Construct validity was determined by correlating the ADDI score to the Physician Global Assessment (PGA) of damage and disease activity. Redundancy of individual items was determined with Cronbach’s alpha.ResultsThe ADDI was validated on a total of 110 paper clinical cases by 37 experts in autoinflammatory diseases. This yielded an ICC of 0.84 (95% CI 0.78 to 0.89). The ADDI score correlated strongly with PGA-damage (r=0.92, 95% CI 0.88 to 0.95) and was not strongly influenced by disease activity (r=0.395, 95% CI 0.21 to 0.55). After comments from disease experts, some item definitions were refined. The interitem correlation in all different categories was lower than 0.7, indicating that there was no redundancy between individual damage items.ConclusionThe ADDI is a reliable and valid instrument to quantify damage in individual patients and can be used to compare disease outcomes in clinical studies.
- Published
- 2018
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