Poor glycemic control in type-2 diabetic patients infected with hepatitis B: A retrospective propensity-matched study

被引:6
作者
Cai, Ting [1 ,2 ]
Yue, Tingting [1 ]
Xu, Ming [1 ]
Zhang, Pan [1 ]
Wang, Yue [1 ]
Liu, Qi [1 ]
Huang, Jie [1 ]
Shen, Ting [2 ]
Yin, Qiang [3 ]
Sheng, Zhifeng [4 ]
Xiao, Yang [4 ]
Deng, Tuo [4 ]
Zhang, Min [5 ,6 ]
De Clercq, Erik [7 ]
Zhang, Chi [2 ]
Li, Guangdi [1 ,3 ]
机构
[1] Cent South Univ, Xiangya Sch Publ Hlth, Hunan Prov Key Lab Clin Epidemiol, Changsha, Peoples R China
[2] Hunan Normal Univ, Hunan Prov Peoples Hosp, Affiliated Hosp 1, Changsha, Peoples R China
[3] Hunan Childrens Hosp, Changsha, Peoples R China
[4] Cent South Univ, Xiangya Hosp 2, Natl Clin Res Ctr Metab Dis, Dept Metab & Endocrinol,Key Lab Diabet Immunol,Hun, Changsha, Hunan, Peoples R China
[5] Cent South Univ, Inst Hepatol, Changsha, Hunan, Peoples R China
[6] Cent South Univ, Xiangya Hosp 2, Dept Infect Dis, Changsha, Hunan, Peoples R China
[7] Katholieke Univ Leuven, Rega Inst Med Res, Dept Microbiol Immunol & Transplantat, Leuven, Belgium
关键词
Glycemic control; HBV; Hemoglobin A1c; Propensity score matching; Type; 2; diabetes; VIRUS INFECTION; INSULIN-RESISTANCE; LIVER-DISEASE; MELLITUS; ASSOCIATION; PREVALENCE; IMPACT; COMPLICATIONS; BURDEN;
D O I
10.1002/jmv.28635
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Hepatitis B virus (HBV) infection and type-2 diabetes mellitus (T2DM) affect millions of individuals worldwide, whereas their interplay remains largely unclear. Here, we analyzed a large cohort of 330 HBV-infected inpatients with T2DM (so-called HBV + T2DM patients) and 330 T2DM inpatients without HBV infection (T2DM patients). Poor glycemic control was defined by glycated hemoglobin (HbA1c) >= 7%. Among 330 HBV + T2DM patients, 252 (76%) aged >= 50 years, 223 (68%) were males, 205 (62%) experienced poor glycemic control. The propensity-score matching approach was applied to match patient age, gender, comorbidities, and antidiabetic treatment between T2DM + HBV and T2DM patients. Compared with T2DM patients, HBV + T2DM patients had poorer glycemic control, longer hospitalization length, and higher alanine aminotransferase (p < 0.05). HBV + T2DM patients with HBV DNA >= 100 IU/mL or HBsAg >= 0.05 IU/mL had worse HbA1c control than T2DM patients without HBV infection (p < 0.05). HBV + T2DM patients who received no anti-HBV therapy had worse HbA1c control than HBV + T2DM patients receiving anti-HBV therapy (p < 0.05). Both insulin and anti-HBV therapy were significant factors associated with glycemic control in HBV + T2DM patients. Overall, HBV + T2DM patients exhibited poorer glycemic control than T2DM patients, but their clinical outcomes were likely improved by insulin plus anti-HBV treatment. Early management of HBV infection likely contributes to better clinical outcomes in HBV-infected patients with T2DM.
引用
收藏
页数:15
相关论文
共 50 条
[31]   Metabolic syndrome and liver-related events: a systematic review and meta-analysis [J].
Ren, Huina ;
Wang, Junna ;
Gao, Yue ;
Yang, Fuwei ;
Huang, Wenxiang .
BMC ENDOCRINE DISORDERS, 2019, 19 (1)
[32]   Prevalence of hepatitis B virus infection among persons with diagnosed diabetes mellitus in the United States, 1999-2010 [J].
Schillie, S. F. ;
Xing, J. ;
Murphy, T. V. ;
Hu, D. J. .
JOURNAL OF VIRAL HEPATITIS, 2012, 19 (09) :674-676
[33]   Propensity Score Matching in Observational Research [J].
Schober, Patrick ;
Vetter, Thomas R. .
ANESTHESIA AND ANALGESIA, 2020, 130 (06) :1616-1617
[34]   Impact of hepatitis B virus infection on hepatic metabolic signaling pathway [J].
Shi, Yi-Xian ;
Huang, Chen-Jie ;
Yang, Zheng-Gang .
WORLD JOURNAL OF GASTROENTEROLOGY, 2016, 22 (36) :8161-8167
[35]   Incidence of diabetes mellitus in a population-based cohort of persons with chronic hepatitis B virus infection [J].
Spradling, P. R. ;
Simons, B. ;
Narayanan, M. ;
Xing, J. ;
Homan, C. ;
Bulkow, L. ;
Cagle, H. ;
Schraer, C. D. ;
McMahon, B. J. .
JOURNAL OF VIRAL HEPATITIS, 2013, 20 (07) :510-513
[36]   Association of glycaemia with macrovascular and microvascular complications of type 2 diabetes (UKPDS 35): prospective observational study [J].
Stratton, IM ;
Adler, AI ;
Neil, HAW ;
Matthews, DR ;
Manley, SE ;
Cull, CA ;
Hadden, D ;
Turner, RC ;
Holman, RR .
BMJ-BRITISH MEDICAL JOURNAL, 2000, 321 (7258) :405-412
[37]  
Ting L., 2021, J MICROBIOL IMMUNOL, V9, P91
[38]   The liver [J].
Trefts, Elijah ;
Gannon, Maureen ;
Wasserman, David H. .
CURRENT BIOLOGY, 2017, 27 (21) :R1147-R1151
[39]   The Global Burden of Liver Disease: The Major Impact of China [J].
Wang, Fu-Sheng ;
Fan, Jian-Gao ;
Zhang, Zheng ;
Gao, Bin ;
Wang, Hong-Yang .
HEPATOLOGY, 2014, 60 (06) :2099-2108
[40]   Guidelines for Prevention and Treatment of Chronic Hepatitis B [J].
Wang, Guiqiang ;
Duan, Zhongping .
JOURNAL OF CLINICAL AND TRANSLATIONAL HEPATOLOGY, 2021, 9 (05) :769-791