Evidence map›Paper›PMID 33842630›Full record

ArticleAnnals of translational medicine2021

A clinical diagnostic model based on an eXtreme Gradient Boosting algorithm to distinguish type 1 diabetes.

Xiaohan Tang, Rui Tang, Xingzhi Sun, Xiang Yan, Gan Huang, Houde Zhou, Guotong Xie, Xia Li, Zhiguang Zhou

Open access · diamondAbstract read
In one paragraph

Article in Annals of translational medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 14 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 4 institutions in 1 country.

Xiaohan TangDepartment of Metabolism and Endocrinology, the Second Xiangya Hospital, Central South University, Changsha, China.
Rui TangDepartment of Intelligent Clinical Decision Support, Ping An Healthcare Technology, Beijing, China.
Xingzhi SunDepartment of Intelligent Clinical Decision Support, Ping An Healthcare Technology, Beijing, China.
Xiang YanDepartment of Metabolism and Endocrinology, the Second Xiangya Hospital, Central South University, Changsha, China.
Gan HuangDepartment of Metabolism and Endocrinology, the Second Xiangya Hospital, Central South University, Changsha, China.
Houde ZhouDepartment of Metabolism and Endocrinology, the Second Xiangya Hospital, Central South University, Changsha, China.
Guotong XieDepartment of Intelligent Clinical Decision Support, Ping An Healthcare Technology, Beijing, China.
Xia LiDepartment of Metabolism and Endocrinology, the Second Xiangya Hospital, Central South University, Changsha, China.
Zhiguang ZhouDepartment of Metabolism and Endocrinology, the Second Xiangya Hospital, Central South University, Changsha, China.
Central South University · CNPing An (China)National Clinical Research Center for Digestive Diseases · CNSecond Xiangya Hospital of Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAccurate classification of type 1 diabetes (T1DM) and type 2 diabetes (T2DM) in the early phase is crucial for individual precision treatment. This study aimed to develop a classification model having fewer and easier to access clinical variables to distinguish T1DM in newly diagnosed diabetes in adults.

methodsClinical and laboratory data were collected from 15,206 adults with newly diagnosed diabetes in this cross-sectional study. This cohort represented 20 provinces and 4 municipalities in China. Types of diabetes were determined based on postprandial C-peptide (PCP) level and glutamic acid decarboxylase autoantibody (GADA) titer. We developed multivariable clinical diagnostic models using the eXtreme Gradient Boosting (XGBoost) algorithm. Classification variables included in the final model were based on their scores of importance. Model performance was evaluated by area under the receiver operating characteristic curve (ROC AUC), sensitivity, and specificity. The performance of models with different variable combinations was compared. Calibration intercept and slope were evaluated for the final model.

resultsAmong the newly diagnosed diabetes cohort, 1,465 (9.63%) persons had T1DM and 13,741 (90.37%) had T2DM. Body mass index (BMI) contributed the most to the model, followed by age of onset and hemoglobin A1c (HbA1c). Compared with models with other clinical variable combinations, a final model that integrated age of onset, BMI and HbA1c had relatively higher performance. The ROC AUC, sensitivity, and specificity for this model were 0.83 (95% CI, 0.80 to 0.85), 0.77, and 0.76, respectively. The calibration intercept and slope were 0.02 (95% CI, -0.03 to 0.06) and 0.90 (95% CI, 0.79 to 1.02), respectively, which suggested a good calibration performance.

conclusionsOur classification model that integrated age of onset, BMI, and HbA1c could distinguish T1DM from T2DM, which provides a useful tool in assisting physicians in subtyping and precising treatment in diabetes.

Indexed as

diagnostic modeleXtreme Gradient Boosting algorithm (XGBoost algorithm)Type 1 diabetes (T1DM)type 2 diabetes (T2DM)

Identifiers

PMID33842630
PMCPMC8033361
OpenAlexW3134623575

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.