Evidence map›Paper›PMID 33833539›Full record

ArticleDiabetes, metabolic syndrome and obesity : targets and therapy2021

Early Predictors in the Onset of Type 2 Diabetes at Different Fasting Blood Glucose Levels.

Xiaomin Xie, Guirong Bai, Huili Liu, Li Zhang, YanTing He, Dan Qiang, Xiaoyan Zou

Abstract read
In one paragraph

Article in Diabetes, metabolic syndrome and obesity : targets and therapy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

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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

7 authors.

Xiaomin Xie *Department of Endocrinology, The First People's Hospital of Yinchuan, Yinchuan, 750001, People's Republic of China.
Guirong Bai *Department of Endocrinology, The First People's Hospital of Yinchuan, Yinchuan, 750001, People's Republic of China.
Huili LiuDepartment of Endocrinology, The First People's Hospital of Yinchuan, Yinchuan, 750001, People's Republic of China.
Li ZhangDepartment of Endocrinology, The First People's Hospital of Yinchuan, Yinchuan, 750001, People's Republic of China.
YanTing HeDepartment of Endocrinology, The First People's Hospital of Yinchuan, Yinchuan, 750001, People's Republic of China.
Dan QiangDepartment of Endocrinology, The First People's Hospital of Yinchuan, Yinchuan, 750001, People's Republic of China.
Xiaoyan ZouDepartment of Endocrinology, The First People's Hospital of Yinchuan, Yinchuan, 750001, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis study investigates the possible roles and potential prediction ability of metabolic parameters in the early development of T2D by detecting their serum levels at different fasting blood glucose (FBG) levels.

methodsThe subjects were included and divided into normal glucose tolerance (NGT), prediabetes (PD), and T2Dsubgroups. Apart from detecting the levels of routine biochemical parameters, fasting serum insulin (FINS), 25(OH)D, thioredoxin-interacting protein (TXNIP), thioredoxin (TRX), and NOD-like receptor family, pyrin domain-containing 3 (NLRP3) were detected. β-cell dysfunction (HOMA-β) and insulin resistance (HOMA-IR) were assessed by homeostasis model assessment. Both univariate and multivariate logistic regression analyses were used to estimate the risk of metabolic parameters, and their optimal cut-off values were obtained in the receiver operating characteristic (ROC) curve analysis and the Youden index.

resultsAmong the 207 subjects, aged from 20 to 60 years (44.62+12.92) contain 118 males and 89 females. There was a significantly lower trend of TRX, HOMA-β, and 25(OH)D following the higher FBG level among these three subgroups, while a significantly higher trend of all the other metabolic parameters. The multivariate analysis showed that subjects with higher values of TRX, HOMA-β, and 25(OH)D had a significantly lower risk for patients to be diagnosed as PD (aOR: 0.945, 0.961, and 0.543) and T2D (aOR: 0.912, 0.947, 0.434). Under the reliable 95% CI, TXNIP with a cut-off value of 119.27 showed the highest AUC value, sensitivity, and specificity (AUC: 0.981, 95% CI: 0.8524-0.9839, 91.49%, and 83.33%) to diagnose PD. FINS with a cut-off value of 28.1 also showed the highest ones (AUC=0.9872, 95% CI: 0.9753-0.9992, 100%, and 92.91%) to diagnose T2D.

conclusionEarly prediction of T2D is vital for timely intervention. Based on the FBG ≥100.8 mg/dl, the results provide evidence that 25(OH)D might be the protective factor in the early development of T2D. Besides, TXNIP and FINS might be the predictor for PD and T2D, respectively.

Indexed as

25-hydroxyvitamin D25(OH)Dinsulin resistancePDprediabetesT2Dthioredoxin-interacting proteinTXNIPtype 2 diabetesβ-cell dysfunction

Identifiers

PMID33833539
PMCPMC8020326

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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.