Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland
Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
J Am Soc Nephrol. 2020 Aug;31(8):1847-1858. doi: 10.1681/ASN.2019101119. Epub 2020 Jul 13.
In 2016, the Food and Drug Administration (FDA) changed labeling regarding metformin contraindications in patients with diabetes and CKD from using serum creatinine-based thresholds to using eGFR-based thresholds. Because race and sex affect serum creatinine levels independently of GFR, the earlier creatinine-based contraindication may have inadvertently caused racial and sex disparities in metformin prescription among patients with low eGFR.
In an analysis of 15,946 Black and White primary care patients with diabetes and eGFR≥30 ml/min per 1.73 m in a large health system (the primary cohort), we assessed the association of race and sex with metformin prescription across eGFR level before and after the FDA label change. For a replication cohort, we meta-analyzed data from 36 cohorts with 1,051,723 patients from OptumLabs Data Warehouse.
In the primary cohort, before the label change, Black patients with eGFR of 30-44 ml/min per 1.73 m were prescribed metformin less often than White counterparts (adjusted prevalence ratio [aPR], 0.65; 95% confidence interval [95% CI], 0.52 to 0.82); this disparity was significantly attenuated after the label change (aPR, 0.90; 95% CI, 0.74 to 1.09; value for interaction by period =0.04). Results were consistent in the replication cohorts. Men with eGFR of 30-44 ml/min per 1.73 m received metformin prescriptions less often than women counterparts before the label change; this was nonsignificantly attenuated after the label change, but we found significant attenuation in the replication cohorts (aPR, 0.76; 95% CI, 0.73 to 0.79; aPR, 0.85; 95% CI, 0.83 to 0.88; value for interaction by period <0.001).
The metformin label change to an eGFR-based contraindication may have reduced racial and sex disparities in metformin prescription in moderate kidney dysfunction.
2016 年,美国食品和药物管理局(FDA)改变了糖尿病和 CKD 患者中二甲双胍禁忌证的标签,从基于血清肌酐的阈值改为基于 eGFR 的阈值。由于种族和性别独立于 GFR 影响血清肌酐水平,因此早期基于肌酐的禁忌证可能无意中导致 eGFR 较低的患者中二甲双胍处方的种族和性别差异。
在一项大型医疗系统中(主要队列),对 15946 名黑人和白人初级保健患者的糖尿病和 eGFR≥30ml/min/1.73m 进行分析,我们评估了种族和性别与 FDA 标签更改前后 eGFR 水平上的二甲双胍处方的相关性。对于一个复制队列,我们对来自 OptumLabs Data Warehouse 的 36 个队列的 1051723 名患者的数据进行了荟萃分析。
在主要队列中,在标签更改之前,eGFR 为 30-44ml/min/1.73m 的黑人患者服用二甲双胍的频率低于白人(调整后的患病率比[aPR],0.65;95%置信区间[95%CI],0.52 至 0.82);标签更改后,这种差异明显减弱(aPR,0.90;95%CI,0.74 至 1.09;时期交互检验值=0.04)。复制队列的结果一致。在标签更改之前,eGFR 为 30-44ml/min/1.73m 的男性接受二甲双胍处方的频率低于女性;标签更改后,这种情况明显减弱,但我们发现复制队列中明显减弱(aPR,0.76;95%CI,0.73 至 0.79;aPR,0.85;95%CI,0.83 至 0.88;时期交互检验值<0.001)。
二甲双胍标签更改为基于 eGFR 的禁忌证可能减少了中度肾功能障碍患者中二甲双胍处方的种族和性别差异。