Dongfang Liu

Dongfang Liu


Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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7 October 2024 in Journal of Diabetes
Verified
Journal Article
Open access
WDWenzhen Deng
Wenzhen Deng
LZLi Zhao
Li Zhao
CCCheng Chen
Cheng Chen
ZRZiyu Ren
Ziyu Ren
YJYuanyuan Jing
Yuanyuan Jing
DLDongfang Liu
Dongfang Liu
Background: In recent years, the prevalence and mortality rates of diabetes have been rising continuously, posing a significant threat to public health and placing a heavy burden on the population. This study was conducted to describe and analyze the burden of diabetes in China from 1990 to 2021 and its attributable risk factors.Methods: Utilizing data from the Global Burden of Disease Study 2021, we analyzed the incidence, prevalence, and disability‐adjusted life years (DALYs) of type 1 diabetes (T1DM) and type 2 diabetes (T2DM) in China from 1990 to 2021. We extracted sex‐ and age‐specific data on diabetes, focusing on DALYs, years lived with disability, and years of life lost. Bayesian meta‐regression and spatiotemporal Gaussian process regression were used to estimate disease parameters. Age‐standardized rates (ASRs) and estimated annual percentage changes (EAPC) were calculated using direct standardization and log‐linear regression. The population‐attributable fractions were also determined for each risk factor.Results: In 2021, the absolute number of incident diabetes mellitus (DM) cases was estimated at 4003543.82, including 32 000 T1DM and 3971486.24 T2DM cases. The ASRs were 244.57 for DM, 2.67 for T1DM, and 241.9 for T2DM (per 100 000 population). The absolute number of prevalent DM cases was 117288553.93, including 1442775.09 T1DM and 115845778.84 T2DM cases. The ASRs were 6142.29 for DM, 86.78 for T1DM, and 6055.51 for T2DM (per 100 000 population). In 2021, there were 178475.73 deaths caused by DM, with an ASR of mortality of 8.98 per 100 000 population. The DALYs due to DM in 2021 were 11713613.86, with an ASR of 585.43 per 100 000 population and an EAPC of 0.57. This increase can be attributed to several factors, including high body mass index, air pollution, and dietary habits.Conclusions: The burden of diabetes is considerable, with high prevalence and incidence rates, highlighting the urgent need for public health interventions. Addressing factors like high fasting plasma glucose, body mass index, air pollution, and dietary risks through effective interventions is critical. image

4 July 2019 in Clinical Endocrinology
Verified
Journal Article
Closed access
PDF file
LTLiang Tang
Liang Tang
LYLei Yuan
Lei Yuan
GYGangyi Yang
Gangyi Yang
FWFeng Wang
Feng Wang
MFMao Fu
Mao Fu
DLDongfang Liu
Dongfang Liu

1 June 2021 in Mechanisms of Ageing and Development
Verified
Journal Article
Closed access
QHQirui He
Qirui He
YLYang Li
Yang Li
WZWeiwei Zhang
Weiwei Zhang
JCJie Chen
Jie Chen
WDWenzhen Deng
Wenzhen Deng
DLDongfang Liu
Dongfang Liu

1 July 2020 in Life Sciences
Verified
Journal Article
Closed access
JFJili Fu
Jili Fu
KNKija Malale Nchambi
Kija Malale Nchambi
HWHao Wu
Hao Wu
XLXie Luo
Xie Luo
XAXizhou An
Xizhou An
DLDongfang Liu
Dongfang Liu

16 March 2023 in Antioxidants & Redox Signaling
Verified
Journal Article
Closed access
YLYang Li
Yang Li
WDWenzhen Deng
Wenzhen Deng
JWJinlin Wu
Jinlin Wu
QHQirui He
Qirui He
GYGangyi Yang
Gangyi Yang
DLDongfang Liu
Dongfang Liu
Aims: Thioredoxin-interacting protein (TXNIP) is a crucial molecular promoter of oxidative stress and has been identified to be associated with cellular senescence. It is an important mediator of β cell insulin secretion and has effects on β cell mass. However, its role in β cell senescence is unclear. The present study was designed to investigate the effects and mechanisms of TXNIP on the senescence and aging- and diet-related dysfunction of β cells. Methods: Human pancreatic paraffin tissues and serum samples from different ages were collected to detect TXNIP expression. TXNIP −/− and C57BL/6J mice were fed either a normal chow diet (NCD) or a high-fat diet (HFD) until 5, 11, 14, or 20 months. The recapitulation experiment was conducted with TXNIP protein injection. MIN6 cells were transfected with LV-TXNIP and LV-siTXNIP. The biochemical indexes, ageing-related markers, cell cycle proteins, and pathways were examined both in vivo and in vitro . Results: TXNIP expression showed an age-related increase in β cells and serum samples from humans. TXNIP significantly impaired glucose metabolism and insulin secretion in an age-dependent manner. TXNIP aggravated age-related and obesity-induced structural failure, oxidative stress, decreased proliferation, increased apoptosis in β cells, and induced the cell cycle arrest. TXNIP interacted with p38 mitogen-activated protein kinase (p38MAPK) and modulated the p16/p21-CDK-Rb axis to accelerate β cell senescence. Innovation and Conclusions: The present study demonstrated that TXNIP may exacerbate pancreatic β cell senescence and age-related dysfunction by inducing cell cycle arrest through the p38-p16/p21-CDK-Rb pathway, in natural and pathological states. Antioxid. Redox Signal . 38, 480–495.

26 June 2024 in GeroScience
Verified
Journal Article
Closed access
PDF file
JLJiangchuan Long
Jiangchuan Long
ZRZiyu Ren
Ziyu Ren
YDYaqian Duan
Yaqian Duan
WTWei Tao
Wei Tao
XLXi Li
Xi Li
DLDongfang Liu
Dongfang Liu