Evidence map›Paper›PMID 42363303›Full record

ArticleDiabetology & metabolic syndrome2026

Severe microvascular disease incidence over a 34-year period among Chinese with newly diagnosed diabetes and impaired glucose tolerance: the Da Qing diabetes outcome study 1986-2020.

Qier An, Jinping Wang, Zhihai Huang, Xinxin Feng, Xin Qian, Shuhan Zhou, Siyao He, Hui Li, Guangwei Li, Yanyan Chen

Abstract read
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Article in Diabetology & metabolic syndrome, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

10 authors.

Qier AnEndocrinology Centre, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100037, China.
Jinping WangDepartment of Cardiology, Da Qing First Hospital, Daqing, Heilongjiang, China.
Zhihai HuangEndocrinology Centre, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100037, China.
Xinxin FengEndocrinology Centre, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100037, China.
Xin QianEndocrinology Centre, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100037, China.
Shuhan ZhouEndocrinology Centre, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100037, China.
Siyao HeEndocrinology Centre, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100037, China.
Hui LiDepartment of Cardiology, Da Qing First Hospital, Daqing, Heilongjiang, China.
Guangwei LiEndocrinology Centre, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100037, China.
Yanyan ChenEndocrinology Centre, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100037, China. dryanyanchen@126.com.

Funding

the Chinese Academy of Medical Sciences Innovation Fund for Medical Sciences 2020-I2M-2-006the National High-Level Hospital Clinical Research Funding of the People's Republic of China 2025-GSP-TS-3US Centers for Disease Control and Prevention and World Health Organization Cooperative Agreement U58/CCU424123-01-02
6 · The paper itself

Abstract

aimsThe aim of this study was to investigate the incidence of severe microvascular disease in adults with newly diagnosed diabetes (NDD), impaired glucose tolerance (IGT) and normal glucose tolerance (NGT) over a 34-year follow-up in China.

methodsThis cohort study enrolled 1631 individuals, including 598 NDD, 540 IGT and 493 NGT initially identified in 1986, who were followed until death, loss to follow-up, or December 31, 2020. Severe microvascular disease was defined as a composite outcome of severe retinopathy, nephropathy, and neuropathy.

resultsDuring the 34-year follow-up, 85.18% (460/540) of the IGT population progressed to diabetes, while 34.89% (172/493) of the NGT subjects developed diabetes. By 2020, severe microvascular disease occurred in 65.03% (95% CI: 58.90%-70.48%) of individuals with NDD, 32.90% (95% CI: 28.19%-37.81%) with IGT, and 16.18% (95% CI: 12.64%-20.11%) with NGT. A comparable trend was observed for the cumulative incidence of each individual microvascular complication component across the three groups. The incidence rate per 1000 person-years was 21.7 in the NDD group, which was higher than that in the IGT (9.7) and NGT (4.4) groups. After adjustment for confounders, the risk of severe microvascular disease was 6.3-fold higher in the NDD group (95% CI: 4.65-8.38, P < 0.0001), and 2.2-fold higher in the IGT group (95% CI: 1.58-2.95, P < 0.001) compared with the NGT group.

conclusionsNDD and IGT in Chinese adults were associated with markedly elevated long-term risk of severe microvascular complications. These findings underscore the importance of achieving optimal glycemic control early in the course of diabetes and implementing intensive lifestyle intervention in IGT to slow or prevent progression to diabetes.

Indexed as

DiabetesImpaired glucose toleranceMicrovascular diseaseNephropathyNeuropathyRetinopathy

Identifiers

PMID42363303
PMCPMC13563904

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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.