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肾功能标志物与二甲双胍的适用情况

Renal function markers and metformin eligibility.

作者信息

Tavares Bello Carlos, Castro Fonseca Ricardo, Sousa Santos Francisco, Sequeira Duarte João, Azinheira Jorge, Vasconcelos Carlos

机构信息

Endocrinology Service, Egas Moniz Hospital, West Lisbon Hospital Center, Lisbon, Portugal -

Endocrinology Service, Egas Moniz Hospital, West Lisbon Hospital Center, Lisbon, Portugal.

出版信息

Minerva Endocrinol. 2018 Sep;43(3):246-252. doi: 10.23736/S0391-1977.17.02626-8. Epub 2017 May 31.

DOI:10.23736/S0391-1977.17.02626-8
PMID:28565889
Abstract

BACKGROUND

Metformin is the cornerstone of the pharmacological therapy for type 2 diabetes mellitus (T2DM). It belongs to the biguanide class of drugs and it improves hepatic insulin resistance and enhances GLP-1 and peptide YY secretion. Despite being considered safe regarding hypoglycemic risk, renal dysfunction remains the main obstacle to its use due to the underlying risk of lactic acidosis. In the recent past many authors used creatinine values as the decisive marker when it came to choose between pharmacological agents in DM. Serum creatinine values equal or above 1.4 and 1.5 mg/dL were considered contraindications for metformin use in women and men respectively. Nowadays, creatinine is not the only surrogate of renal dysfunction and formulas such as the MDRD and CKD-EPI, that besides serum creatinine also include variables such as gender, age and race, have replaced serum creatinine as the standard for renal function assessment. Furthermore, since the associations between metformin and lactic acidosis in renal disease are not straightforward, its use has been considered safe down to creatinine clearances of 30 mL/min/1.73 m2. The authors describe a population with T2DM being treated with metformin and evaluate the impact of the solo evaluation of serum creatinine or CKD-EPI on biguanide prescription.

METHODS

Retrospective, observational, single-center study. All type 2 diabetic patients with regular follow up in a Central University Hospital Endocrinology-Diabetology Outpatient Clinic who were being treated with metformin and had at least 2 creatinine and estimated glomerular filtration rate (eGFR) measurements in the last decade were included. Patients were stratified according to renal function-based metformin contraindication criteria: creatinine group included patients with serum creatinine levels above 1.4 and 1.5 mg/dL in women and men respectively, and eGFR group included patients with eGFR below 30 mL/min/1.73 m2. The entire population and both groups are described and compared regarding comorbidities, demographic and laboratory data. The authors report the impact of each renal function marker (serum creatinine or eGFR) when used solo regarding metformin prescription eligibility.

RESULTS

A total of 2218 patients (61.3% females) with a mean age of 70±12 years is studied. Mean diabetes duration was 11.8±8.8 years. No cases with an eGFR below 30 mL/min/1.73 m2 were identified. On the other hand, in patients with GFR greater than 30 mL/min/1.73 m2, creatinine alone would contraindicate therapy in 274 patients (12.4% of the study population). Comparing Stage 3 chronic kidney disease patients without creatinine contraindication criteria with those with creatinine based contraindication, the data reveals that a higher prevalence of males, with longer diabetes duration, higher target organ damage (cerebrovascular disease, peripheral artery disease, heart failure, neuropathy and retinopathy) and with worse glycemic control were prevalent more in the elevated creatinine group. The use of serum creatinine as the single marker for renal function would significantly reduce metformin eligibility (OR=0.88, 95% CI: 0.8-0.95, P=0.002).

CONCLUSIONS

Metformin is the first line pharmacological agent in type 2 diabetes mellitus patients, being associated with significant HbA1c reductions and improvements in both micro and macrovascular outcomes. Avoiding its use due to imprecise renal function markers would potentially render the patient deprived of optimal pharmacological therapy for T2DM. Creatinine contraindication criteria alone are associated with unnecessary under prescription of metformin.

摘要

背景

二甲双胍是2型糖尿病(T2DM)药物治疗的基石。它属于双胍类药物,可改善肝脏胰岛素抵抗,并增强胰高血糖素样肽-1(GLP-1)和酪酪肽(PYY)的分泌。尽管在低血糖风险方面被认为是安全的,但由于存在乳酸酸中毒的潜在风险,肾功能不全仍然是其使用的主要障碍。过去,许多作者在糖尿病患者选择药物时将肌酐值作为决定性指标。血清肌酐值等于或高于1.4 mg/dL和1.5 mg/dL分别被视为女性和男性使用二甲双胍的禁忌证。如今,肌酐已不是肾功能不全的唯一替代指标,诸如肾脏病饮食改良(MDRD)公式和慢性肾脏病流行病学合作(CKD-EPI)公式等,除血清肌酐外还纳入了性别、年龄和种族等变量,已取代血清肌酐成为评估肾功能的标准。此外,由于二甲双胍与肾脏疾病中乳酸酸中毒之间的关联并不直接,其在肌酐清除率低至30 mL/min/1.73 m²时的使用也被认为是安全的。作者描述了一个接受二甲双胍治疗的T2DM患者群体,并评估单独评估血清肌酐或CKD-EPI对双胍类药物处方的影响。

方法

回顾性、观察性、单中心研究。纳入所有在某中心大学医院内分泌-糖尿病门诊定期随访、正在接受二甲双胍治疗且在过去十年中至少有2次肌酐和估算肾小球滤过率(eGFR)测量值的2型糖尿病患者。根据基于肾功能的二甲双胍禁忌标准对患者进行分层:肌酐组包括血清肌酐水平分别高于1.4 mg/dL和1.5 mg/dL的女性和男性患者,eGFR组包括eGFR低于30 mL/min/1.73 m²的患者。描述并比较了整个人群以及两组患者的合并症、人口统计学和实验室数据。作者报告了单独使用每种肾功能指标(血清肌酐或eGFR)对二甲双胍处方资格的影响。

结果

共研究了2218例患者(61.3%为女性),平均年龄为70±12岁。平均糖尿病病程为11.8±8.8年。未发现eGFR低于30 mL/min/1.73 m²的病例。另一方面,在GFR大于30 mL/min/1.73 m²的患者中,仅肌酐一项指标就会使274例患者(占研究人群的12.4%)的治疗成为禁忌。将无肌酐禁忌标准的3期慢性肾脏病患者与有基于肌酐的禁忌证的患者进行比较,数据显示,肌酐升高组中男性患病率更高,糖尿病病程更长,靶器官损害(脑血管疾病、外周动脉疾病、心力衰竭、神经病变和视网膜病变)更多,血糖控制更差。将血清肌酐作为肾功能的单一指标会显著降低二甲双胍的适用率(OR=0.88,95%CI:0.8 - 0.95,P=0.002)。

结论

二甲双胍是2型糖尿病患者的一线药物,与糖化血红蛋白(HbA1c)显著降低以及微血管和大血管结局改善相关。由于肾功能指标不准确而避免使用二甲双胍可能会使患者无法获得T2DM的最佳药物治疗。仅肌酐禁忌标准与二甲双胍不必要的处方不足有关。

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