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Association of Metformin Use with Iron Deficiency Anemia in Urban Chinese Patients with Type 2 Diabetes
被引:2
|作者:
Wu, Junhui
[1
]
Yang, Ruotong
[2
]
Yu, Huan
[2
]
Qin, Xueying
[2
,3
]
Wu, Tao
[2
,3
]
Wu, Yiqun
[2
,3
]
Hu, Yonghua
[2
,3
,4
]
机构:
[1] Peking Univ, Sch Nursing, Beijing 100191, Peoples R China
[2] Peking Univ, Sch Publ Hlth, Dept Epidemiol & Biostat, Beijing 100191, Peoples R China
[3] Peking Univ, Key Lab Epidemiol Major Dis, Minist Educ, Beijing 100191, Peoples R China
[4] Peking Univ, Med Informat Ctr, Beijing 100191, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
metformin;
iron-deficiency anemia;
type;
2;
diabetes;
cohort study;
pleiotropic effects;
CARTILAGE DEGENERATION;
GLYCEMIC CONTROL;
TRENDS;
D O I:
10.3390/nu15143081
中图分类号:
R15 [营养卫生、食品卫生];
TS201 [基础科学];
学科分类号:
100403 ;
摘要:
Background: Previous evidence yielded contradictory findings on the relationship between metformin and anemia. This study aims to assess whether metformin use is associated with iron-deficiency anemia (IDA) risk in patients with type 2 diabetes (T2D) in Beijing, China. Methods: Overall, 60,327 newly diagnosed T2D patients were included based on a historical cohort study design. The information pertaining to these patients was gathered from the Beijing Medical Claim Data for Employees Database. These patients were then categorized into the metformin and non-metformin groups and matched on a 1:1 propensity score based on their initial antidiabetic prescription. The Cox proportional hazards models were utilized to calculate the incidences and the hazard ratios (HRs). Results: The study enrolled 27,960 patients with type 2 diabetes, with 13,980 patients in each of the initial glucose-lowering prescription groups: metformin and non-metformin. During a median follow-up period of 4.84 years, 4832 patients developed IDA. The incidence of IDA was significantly lower in the metformin group (26.08/1000 person-years) than in the non-metformin group (43.20/1000 person-years). Among the three groups divided by the proportion of days covered by metformin, we found a negative correlation between the proportion of days covered by metformin and the risk of IDA. The risk of IDA in patients with a proportion of days covered by metformin of <20%, 20-79%, and & GE;80% was 0.43 (0.38, 0.48), 0.37 (0.34, 0.42), and 0.91 (0.85, 0.98), respectively, compared to the non-metformin group. We also performed subgroup analyses and sensitivity analyses: the incidence of IDA in the metformin group was lower than that in the non-metformin group in all subgroups, and the protective effect was more significant in subgroups of patients aged & GE;65, with Charlson comorbidity index (CCI) & GE;2, and with gastric acid inhibitor use. Conclusions: In Chinese patients with T2DM, metformin treatment was associated with a decreased risk of IDA admission, and this risk responded positively to the proportion of days covered by metformin. These findings suggest that metformin may have a pleiotropic effect on IDA in patients with type 2 diabetes. Our study has important clinical implications for the management of patients with diabetes and other conditions that increase the risk of IDA.
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