Identification of predictive factors of diabetic ketoacidosis in type 1 diabetes using a subgroup discovery algorithm

Author:

Ibald‐Mulli Angela1ORCID,Seufert Jochen2ORCID,Grimsmann Julia M.34ORCID,Laimer Markus5,Bramlage Peter6ORCID,Civet Alexandre7,Blanchon Margot7,Gosset Simon7,Templier Alexandre7,Paar W. Dieter8,Zhou Fang Liz9ORCID,Lanzinger Stefanie34ORCID

Affiliation:

1. Real World Evidence and Clinical Outcome Generation, Sanofi Paris France

2. Division of Endocrinology and Diabetology, Department of Medicine II, Medical Center – University of Freiburg, Faculty of Medicine University of Freiburg Freiburg Germany

3. Institute of Epidemiology and Medical Biometry, ZIBMT Ulm University Ulm Germany

4. German Centre for Diabetes Research (DZD) München‐Neuherberg Germany

5. Department of Diabetes, Endocrinology, Nutritional Medicine and Metabolism, Inselspital, Bern University Hospital University of Bern Bern Switzerland

6. Institute for Pharmacology and Preventive Medicine Cloppenburg Germany

7. Quinten Paris France

8. Sanofi‐Aventis Deutschland GmbH Berlin Germany

9. Sanofi Bridgewater New Jersey USA

Abstract

AbstractAimTo identify predictive factors for diabetic ketoacidosis (DKA) by retrospective analysis of registry data and the use of a subgroup discovery algorithm.Materials and MethodsData from adults and children with type 1 diabetes and more than two diabetes‐related visits were analysed from the Diabetes Prospective Follow‐up Registry. Q‐Finder, a supervised non‐parametric proprietary subgroup discovery algorithm, was used to identify subgroups with clinical characteristics associated with increased DKA risk. DKA was defined as pH less than 7.3 during a hospitalization event.ResultsData for 108 223 adults and children, of whom 5609 (5.2%) had DKA, were studied. Q‐Finder analysis identified 11 profiles associated with an increased risk of DKA: low body mass index standard deviation score; DKA at diagnosis; age 6‐10 years; age 11‐15 years; an HbA1c of 8.87% or higher (≥ 73 mmol/mol); no fast‐acting insulin intake; age younger than 15 years and not using a continuous glucose monitoring system; physician diagnosis of nephrotic kidney disease; severe hypoglycaemia; hypoglycaemic coma; and autoimmune thyroiditis. Risk of DKA increased with the number of risk profiles matching patients’ characteristics.ConclusionsQ‐Finder confirmed common risk profiles identified by conventional statistical methods and allowed the generation of new profiles that may help predict patients with type 1 diabetes who are at a greater risk of experiencing DKA.

Funder

Sanofi

Publisher

Wiley

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine

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