Improving renoprotective effects by adding piperazine ferulate and angiotensin receptor blocker in diabetic nephropathy: a meta-analysis of randomized controlled trials
Autor: | Qiong Cheng, Yenjen Chen, Wenhsing Yang, Wei Chen, Chiehlun Yang |
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Rok vydání: | 2021 |
Předmět: |
Nephrology
medicine.medical_specialty Angiotensin receptor Urology 030232 urology & nephrology 030204 cardiovascular system & hematology Diabetic nephropathy Angiotensin Receptor Antagonists 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Internal medicine Humans Medicine Diabetic Nephropathies Piperazine Blood urea nitrogen Randomized Controlled Trials as Topic Kidney Creatinine Proteinuria business.industry medicine.disease medicine.anatomical_structure chemistry Drug Therapy Combination medicine.symptom business |
Zdroj: | International Urology and Nephrology. 54:299-307 |
ISSN: | 1573-2584 0301-1623 |
DOI: | 10.1007/s11255-021-02927-2 |
Popis: | Piperazine ferulate, a derivative of ferulic acid has been widely used in clinical practice for cardiovascular and kidney diseases in China. The objective of this meta-analysis was to investigate the benefits by adding piperazine ferulate to angiotensin receptor blockers (ARBs) in diabetic nephropathy patients. PubMed, Embase, Cochrane Library, Wangfang, VIP, and CNKI database (until March 17, 2021) were comprehensively searched for randomized controlled trials investigating the effects of adding piperazine ferulate to ARBs in diabetic nephropathy patients. Data were retrieved from 14 RCTs involving 1374 patients. When compared with ARBs alone, co-administration of piperazine ferulate and ARBs significantly reduced urinary albumin excretion rate (weighted mean differences [WMD] − 20.32 μg/min; 95% confidence interval [CI] − 28.45 to − 12.19), 24-h proteinuria (WMD − 91.08 mg; 95% CI − 107.24 to − 74.91), β2-microglobulin (standard mean difference [SMD] − 2.07; 95% CI − 2.51 to − 1.63), serum level of creatinine (WMD − 8.39 μmol/L; 95% CI − 11.87 to − 4.92), fibrinogen (WMD − 0.40 g/L; 95% CI − 0.46 to − 0.33), and plasma viscosity (WMD − 0.56 mPa s; 95% CI − 0.91 to − 0.21). Subgroup analysis showed that the effects of piperazine ferulate on UAER and serum creatinine were stronger in early diabetic nephropathy. However, piperazine ferulate had no significant effects on the serum blood urea nitrogen and fasting blood glucose. Adding piperazine ferulate to ARBs may achieve additional renal protective benefits, particular in early diabetic nephropathy patients. |
Databáze: | OpenAIRE |
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