M. Saito, Yoshihiro Ishida, H. Yoshida, Yuka Irie, N. Terakawa, A. Iwai
{"title":"Influence of Anti-Hyperlipidemic Agents on Renal Functions of Patients Having Normal Kidney.","authors":"M. Saito, Yoshihiro Ishida, H. Yoshida, Yuka Irie, N. Terakawa, A. Iwai","doi":"10.5649/JJPHCS1975.26.443","DOIUrl":null,"url":null,"abstract":"Acute coronary syndrome (ACS) was recently revealed to occur when a fragile plaque in a fibrous capsule breaks off and a thrombus produced at the broken site obstructs the vascular cavity. Anti-hyperlipidemic agents have been reported to be effective in preventing this onset of ACS through its stabilizing effect on these plaques, thereby leading to its extensive application. However, no reports have yet comparatively examined the influence of two combined antihyperlipidemic agents of different species on the renal functions including blood urea nitrogen (BUN) and serum creatinine (Scr) in patients whose kidneys function normally. Therefore, BUN, total cholesterol (TC), neutral triglyceride (TG), high density lipoprotein (HDL), and low density lipoprotein (LDL) were comparatively analyzed before and one year after treatment with single pravastatin (CS), single bezafibrate (BF) or CS-F BF combination in patients first diagnosed to have hyperlipidemia at our hospital. While TC and LDL significantly decreased in the CS group, TG significantly decreased and HDL significantly increased in the BF group. In the CS-FBF combination group, TC, TG and LDL significantly decreased while HDL significantly increased. In the three groups, no significant increase was detected for BUN or Scr. As mentioned above, the administration of CS and BF to patients with normal renal functions therefore appears to be safe since no renal disturbances were observed.","PeriodicalId":14621,"journal":{"name":"Japanese Journal of Hospital Pharmacy","volume":"34 1","pages":"443-450"},"PeriodicalIF":0.0000,"publicationDate":"2000-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Japanese Journal of Hospital Pharmacy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5649/JJPHCS1975.26.443","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Acute coronary syndrome (ACS) was recently revealed to occur when a fragile plaque in a fibrous capsule breaks off and a thrombus produced at the broken site obstructs the vascular cavity. Anti-hyperlipidemic agents have been reported to be effective in preventing this onset of ACS through its stabilizing effect on these plaques, thereby leading to its extensive application. However, no reports have yet comparatively examined the influence of two combined antihyperlipidemic agents of different species on the renal functions including blood urea nitrogen (BUN) and serum creatinine (Scr) in patients whose kidneys function normally. Therefore, BUN, total cholesterol (TC), neutral triglyceride (TG), high density lipoprotein (HDL), and low density lipoprotein (LDL) were comparatively analyzed before and one year after treatment with single pravastatin (CS), single bezafibrate (BF) or CS-F BF combination in patients first diagnosed to have hyperlipidemia at our hospital. While TC and LDL significantly decreased in the CS group, TG significantly decreased and HDL significantly increased in the BF group. In the CS-FBF combination group, TC, TG and LDL significantly decreased while HDL significantly increased. In the three groups, no significant increase was detected for BUN or Scr. As mentioned above, the administration of CS and BF to patients with normal renal functions therefore appears to be safe since no renal disturbances were observed.
急性冠状动脉综合征(ACS)最近被发现是当纤维囊内脆弱的斑块破裂并在破裂部位产生血栓阻塞血管腔时发生的。据报道,抗高脂血症药物通过对这些斑块的稳定作用有效地预防ACS的发生,从而导致其广泛应用。然而,两种不同种类的联合抗高脂血药对肾功能正常患者血尿素氮(BUN)和血清肌酐(Scr)的影响尚未见比较报道。因此,比较分析我院首次诊断为高脂血症患者单药普伐他汀(CS)、单药贝扎贝特(BF)或CS- f BF联合治疗前后1年的BUN、总胆固醇(TC)、中性甘油三酯(TG)、高密度脂蛋白(HDL)、低密度脂蛋白(LDL)。CS组TC和LDL显著降低,BF组TG显著降低,HDL显著升高。CS-FBF联合组TC、TG、LDL显著降低,HDL显著升高。在三组中,BUN或Scr均未显著升高。如上所述,由于未观察到肾脏紊乱,因此对肾功能正常的患者给予CS和BF似乎是安全的。