Effects of colchicine use on ischemic and hemorrhagic stroke risk in diabetic patients with and without gout

被引:4
|
作者
Yeh, Jun-Jun [1 ,2 ]
Kuo, I-Ling [3 ]
Yip, Hei-Tung [4 ,5 ]
Hsueh, Min-Yuan [1 ]
Hsu, Chung-Y [6 ,7 ]
Kao, Chia-Hung [6 ,7 ,8 ,9 ,10 ,11 ]
机构
[1] Ditmanson Med Fdn Chia Yi Christian Hosp, Dept Family Med & Med Res, Chiayi, Taiwan
[2] China Med Univ, Taichung, Taiwan
[3] Chia Yi Christian Hosp, Ditmanson Med Fdn, Dept Nutr, Chiayi, Taiwan
[4] China Med Univ Hosp, Management Off Hlth Data, Taichung, Taiwan
[5] China Med Univ, Coll Med, Taichung, Taiwan
[6] China Med Univ, Coll Med, Grad Inst Biomed Sci, 2 Yuh Der Rd, Taichung 404, Taiwan
[7] China Med Univ, Coll Med, Sch Med, 2 Yuh Der Rd, Taichung 404, Taiwan
[8] China Med Univ Hosp, Ctr Augmented Intelligence Healthcare, Taichung, Taiwan
[9] China Med Univ Hosp, Dept Nucl Med, Taichung, Taiwan
[10] China Med Univ Hosp, PET Ctr, Taichung, Taiwan
[11] Asia Univ, Dept Bioinformat & Med Engn, Taichung, Taiwan
关键词
COMPLICATIONS SEVERITY INDEX; C-REACTIVE PROTEIN; MORTALITY; HEMOGLOBIN;
D O I
10.1038/s41598-022-13133-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
This study aimed to determine the effect of colchicine use on the risk of stroke among patients with diabetes mellitus (DM). We retrospectively enrolled patients with DM between 2000 and 2013 from the Longitudinal Health Insurance Database and divided them into a colchicine cohort (n = 8761) and noncolchicine cohort (n = 8761) by using propensity score matching (PSM). The event of interest was a stroke, including ischemic stroke and hemorrhagic stroke. The incidence of stroke was analyzed using multivariate Cox proportional hazards models between the colchicine cohort and the comparison cohort after adjustment for several confounding factors. The subdistribution hazard model was also performed for examination of the competing risk. The colchicine cohort had a significantly lower incidence of stroke [adjusted hazard ratios (aHR), 95% confidence intervals (95%CI)] (aHR = 0.61, 95%CI = 0.55-0.67), ischemic stroke (aHR = 0.59, 95%CI = 0.53-0.66), and hemorrhagic stroke (aHR = 0.66, 95%CI = 0.53-0.82) compared with the noncolchicine cohort. Drug analysis indicated that patients in the colchicine cohort who received colchicine of cumulative daily defined dose (cDDD) > 14 and duration > 28 days had a lower risk of stroke and ischemic stroke compared with nonusers. The colchicine cohort (cDDD > 150, duration > 360 days) also had a lower risk of stroke, ischemic stroke, and hemorrhagic stroke. The cumulative incidence of stroke, ischemic stroke, and hemorrhagic stroke in the colchicine cohort was significantly lower than that in the noncolchicine cohort (log-rank P < 0.001). However, the subdistribution hazard model reveal the colchicine was not associated with the hemorrhagic stroke in DM patients without gout (aHR = 0.69, 95%CI = 0.47-1.00). Colchicine use with cDDD > 14 and duration > 28 days was associated with lower risk of stroke and ischemic stroke, and colchicine use with cDDD > 150 and duration > 360 days played an auxiliary role in the prevention of stroke, ischemic stroke, and hemorrhagic stroke in patients with DM. The colchicine for the hemorrhagic stroke in DM patients without gout seem to be null effect.
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页数:14
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