with type 2 diabetes mellitus

被引:12
|
作者
Wu, Szu-Yuan [1 ,2 ,3 ,4 ,5 ,6 ,7 ]
Chen, Wan -Ming [1 ,2 ]
Chen, Yi-Chan [8 ]
Chiang, Ming-Feng [9 ]
Lee, Ming-Che [10 ]
Soong, Ruey-Shyang [10 ,11 ]
机构
[1] Fu Jen Catholic Univ, Grad Inst Business Adm 1, Coll Management, New Taipei, Taiwan
[2] Fu Jen Catholic Univ, Artificial Intelligence Dev Ctr, New Taipei, Taiwan
[3] Asia Univ, Coll Med & Hlth Sci, Dept Food Nutr & Hlth Biotechnol, Taichung, Taiwan
[4] Lo Hsu Med Fdn, Lotung Poh Ai Hosp, Big Data Ctr, Yilan, Taiwan
[5] Lotung Poh Ai Hosp, Lo Hsu Med Fdn, Div Radiat Oncol, Yilan, Taiwan
[6] Asia Univ, Coll Med & Hlth Sci, Dept Healthcare Adm, Taichung, Taiwan
[7] Taipei Med Univ, Taipei Municipal Wan Fang Hosp, Ctr Reg Anesthesia & Pain Med, Taipei, Taiwan
[8] Chang Gung Mem Hosp, Dept Gen Surg, Keelung, Taiwan
[9] Lotung Poh Ai Hosp, Lo Hsu Med Fdn, Dept Internal Med, Div Gastroenterol & Hepatol, Yilan 265, Taiwan
[10] Taipei Med Univ, Coll Med, Taipei, Taiwan
[11] Taipei Municipal Wanfang Hosp, Dept Surg, Div Transplantat, Taipei, Taiwan
关键词
H1-Antihistamines; Hepatocellular Carcinoma; incidence rate ratio; Type 2 Diabetes Mellitus; dose; -dependent; HEPATOCELLULAR-CARCINOMA; NATURAL-HISTORY; LIVER-DISEASE; CANCER-RISK; ASSOCIATION; INCREASES; STATEMENT; HISTAMINE; METFORMIN; THERAPY;
D O I
10.1016/j.diabet.2022.101393
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose: H1-antihistamines (AHs) may exert protective effects against cancer. We investigated the association of AH use with hepatocellular carcinoma (HCC) risk in type 2 diabetes mellitus (T2DM) patients without hepatitis B virus (HBV) or hepatitis C virus (HCV) infection. Methods: The data of patients with T2DM enrolled from Taiwan's National Health Insurance Research Database were examined for the period of January 1, 2008, to December 31, 2018. We used the Kaplan-Meier method and Cox proportional hazards regression to evaluate the AH use-HCC risk association. Results: After 1:1 propensity score matching was performed, the two cohorts were each divided into AH users (n = 47,990) and nonusers (n = 47,990). The risk of HCC was significantly lower in AH users than in AH nonusers (adjusted hazard ratio [aHR]: 0.55 95% confidence interval [95% CI], 0.46 to 0.67; IRR: 0.70; 95% CI, 0.60 to 0.84), respectively. The dose-response relationship between AH use and HCC risk was also observed (aHRs: 0.58, 0.56, 0.50, and 0.41 for 28-35, 36-49, 50-77, and >77 cumulative defined daily doses of AH, respectively). Conclusion: AH use can reduce HCC risk in T2DM patients without HBV or HCV infection in a dose-dependent manner.
引用
收藏
页数:9
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