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Clinical prediction model for MODY type diabetes mellitus in children

https://doi.org/10.14341/DM13091

Abstract

BACKGROUND: MODY (maturity-onset diabetes of the young) is a rare monogenic form of diabetes mellitus, the gold standard of diagnosis is mutations detection in the genes responsible for the development of this form diabetes. Genetic test is expensive and takes a lot of time. The diagnostic criteria for MODY are well known. The development of clinical decision support system (CDSS) which allows physicians based on clinical data to determine who should have molecular genetic testing is relevant.

AIM: Provided a retrospective analysis of clinical data of the patients with T1DM and MODY, from 0 to 18 years old, regardless of the duration of the disease to develop the model. Based on clinical data, a feedforward neural network (NN) was implemented - a multilayer perceptron.

MATERIALS AND METHODS: Development of the most effective algorithm for predicting MODY in children based on available clinical indicators of 1710 patients with diabetes under the age of 18 years using a multilayer feedforward neural network.

RESULTS: The sample consisted of 1710 children under the age of 18 years with T1DM (78%) and MODY (22%) diabetes. For the final configuration of NS the following predictors were selected: gender, age at passport age, age at the diagnosis with DM, HbA1c, BMI SDS, family history of DM, treatment. The performance (quality) assessment of the NN was carried out on a test sample (the area under the ROC (receiver operating characteristics) curve reached 0.97). The positive predictive value of PCPR was achieved at a cut-off value of 0.40 (predicted probability of MODY diabetes 40%). At which the sensitivity was 98%, specificity 93%, PCR with prevalence correction was 78%, and PCR with prevalence correction was 99%, the overall accuracy of the model was 94%.

Based on the NN model, a CDSS was developed to determine whether a patient has MODY diabetes, implemented as an application.

CONCLUSION: The clinical prediction model MODY developed in this work based on the NN, uses the clinical characteristic available for each patient to determine the probability of the patient having MODY. The use of the developed model in clinical practice will assist in the selection of patients for diagnostic genetic testing for MODY, which will allow for the efficient allocation of healthcare resources, the selection of personalized treatment and patient monitoring.

About the Authors

D. N. Laptev
Endocrinology Research Centre
Russian Federation

Dmitry N. Laptev - MD, PhD.

Moscow


Competing Interests:

none



E. A. Sechko
Endocrinology Research Centre
Russian Federation

Elena A. Sechko - MD, PhD; Researcher ID: S-4114-2016; Scopus Author ID: 55880018700.

11 Dm. Ulyanova street, 117036 Moscow


Competing Interests:

none



E. M. Romanenkova
Endocrinology Research Centre
Russian Federation

Elizaveta M. Romanenkova - MD.; Researcher ID: AAB-7186-2021; eLibrary SPIN: 6190-0118.

Moscow


Competing Interests:

none



I. A. Eremina
Endocrinology Research Centre
Russian Federation

Irina A. Eremina - MD, PhD.; Researcher ID: S-3979-2016; Scopus Author ID: 6701334405.

Moscow


Competing Interests:

none



O. B. Bezlepkina
Endocrinology Research Centre
Russian Federation

Olga B. Bezlepkina - MD, PhD; Researcher ID: B-6627-2017; Scopus Author ID: 6507632848.

Moscow


Competing Interests:

none



V. A. Peterkova
Endocrinology Research Centre
Russian Federation

Valentina A. Peterkova - MD, PhD, Professor, academician of Russian Academy of Medical Sciences.

Moscow


Competing Interests:

none



N. G. Mokrysheva
Endocrinology Research Centre
Russian Federation

Natalya G. Mokrysheva - MD, PhD, Professor.

Moscow


Competing Interests:

none



References

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10. Besser REJ, et al. Urinary C-Peptide Creatinine Ratio Is a Practical Outpatient Tool for Identifying Hepatocyte Nuclear Factor 1-α/Hepatocyte Nuclear Factor 4-α Maturity-Onset Diabetes of the Young From Long-Duration Type 1 Diabetes // Diabetes Care. 2011. Vol. 34, № 2. P. 286–291. https://doi.org/10.2337/dc10-1293

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12. Sechko EA, Romanenkova EM, Eremina IA, et al. The role of specific pancreatic antibodies in the differential diagnosis of complete clinical and laboratory remission of type 1 diabetes mellitus and MODY in children. Diabetes mellitus. 2022;25(5):449-457. (In Russ.)] https://doi.org/10.14341/DM12921

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Supplementary files

1. Figure 1. Neural network configuration.
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2. Figure 2. Model performance indicators depending on the number of predictors in the process of their sequential addition according their statistical value. Overall accuracy and AUC on the main axis, error on the minor axis.
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3. Figure 3. Operational characteristics of the final neural network configuration obtained on the test sample.
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4. Figure 4. Loss function when training a neural network for training and validation samples.
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5. Figure 5. Model performance indicators depending on the chosen threshold value of the predicted probability.
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6. Figure 6. Implementation of a mathematical model developed by a neural network in the form of a medical decision support system.
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Review

For citations:


Laptev D.N., Sechko E.A., Romanenkova E.M., Eremina I.A., Bezlepkina O.B., Peterkova V.A., Mokrysheva N.G. Clinical prediction model for MODY type diabetes mellitus in children. Diabetes mellitus. 2024;27(1):33-40. (In Russ.) https://doi.org/10.14341/DM13091

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ISSN 2072-0351 (Print)
ISSN 2072-0378 (Online)