吉非罗齐治疗提高高密度脂蛋白水平的疗效。

Artery Pub Date : 1992-01-01
S Weis, B J Kudchodkar, M B Clearfield, A G Lacko
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引用次数: 0

摘要

本研究选取30例受试者,5例正常甘油三酯(NTG)伴低HDL- c (HDL- c < 35 mg/dl), 25例高甘油三酯(HTG)伴低HDL- c和高HDL- c (HDL- c > 35 mg/dl)。给予吉非罗齐(BID 600 mg)治疗12周。在两组中,吉非罗齐均显著降低血清TG水平(p < 0.005),而HDL-C仅在HTG患者中显著升高(p < 0.005)。HDL-C水平的变化是高度可变的(-40 - 50%),似乎依赖于治疗期间达到的血清TG水平。根据治疗后血清TG水平将HTG患者分为两组。1组血清TG < 100mg /dL, 2组血清TG > 100mg /dL。治疗后,只有第1组的HDL-C显著升高(p < 0.005)。两组治疗前血清TG、HDL-C水平相近,但1组LDL-C显著高于对照组(p < 0.025)。预处理血清LDL-C与治疗期间HDL-C升高呈正相关(r = 0.51, p < 0.01, n = 25)。因此,根据患者的初始血清LDL-C水平将患者分为三组(第一组:LDL-C < 130 mg/dl)。组2:LDL-C, 130-159 mg/dl,组3:LDL-C > 160 mg/dl)。只有第3组在治疗后HDL-C水平显著升高。三组患者血清TG、HDL-C预处理水平差异无统计学意义。初始体重(r = -0.43 p < 0.025, n = 30)和治疗期间体重变化百分比(r = -0.47, p < 0.025, n = 30)与血清TG降低百分比呈负相关。体重变化与高密度脂蛋白胆固醇变化呈显著负相关(r = -0.48, p < 0.25, n = 30)。我们得出的结论是,对于初始LDL胆固醇水平相对较高的HTG患者(Fredrickson's IIb型表型),gemfibrozil在降低血清甘油三酯、LDL- c和增加血清hdl -胆固醇方面最有效。为了有效改善大多数HTG患者的hdl -胆固醇,需要将血清TG水平降至100mg /dl以下。此外,治疗期间体重减轻可能会显著增强吉非罗齐治疗的益处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The efficacy of gemfibrozil therapy for raising high density lipoprotein levels.

Thirty subjects, 5 normotriglyceridemic (NTG) with low HDL cholesterol (HDL-C < 35 mg/dl) and 25 hypertriglyceridemic (HTG) with low and high HDL-C (HDL-C > 35 mg/dl) were selected fo this study. They were treated with gemfibrozil (600 mg BID) for 12 weeks. In both groups, gemfibrozil significantly reduced serum TG levels (p < 0.005), yet HDL-C increased significantly only in HTG patients (p < 0.005). The changes in HDL-C levels were highly variable (-40 to 50%) and appeared to be dependent on the levels of serum TG achieved during treatment. Based on post-treatment serum TG, the HTG patients were divided into 2 groups. Group 1 with serum TG of < 100 mg/dL and Group 2 with serum TG levels > 100 mg/dl. Significant post treatment increases in HDL-C were seen only in Group 1 (p < 0.005). The two groups had similar pretreatment serum TG and HDL-C levels but the LDL-C was significantly higher in Group 1 (p < 0.025). Pretreatment serum LDL-C also correlated positively with the increases in HDL-C during treatment (r = 0.51, p < 0.01, n = 25). Consequently, the patients were divided into three groups based on their initial serum LDL-C levels (Group 1: LDL-C < 130 mg/dl. Group 2: LDL-C, 130-159 mg/dl and Group 3: LDL-C > 160 mg/dl). The HDL-C levels increased significantly upon treatment only in Group 3. Pretreatment levels of serum TG and HDL-C were not significantly different among the three groups. Initial body weight (r = -0.43 p < 0.025, n = 30) and percent change in body weight during treatment (r = -0.47, p < 0.025, n = 30) correlated negatively with the percent reduction in serum TG. The change in body weight also showed significant negative correlation with the changes in HDL cholesterol (r = -0.48, p < 0.25, n = 30). We conclude that gemfibrozil is most effective in reducing serum triglycerides, LDL-C and increasing serum HDL-cholesterol in HTG patients who also have comparatively high initial LDL cholesterol levels (Fredrickson's type IIb phenotype). For effective improvement of HDL-cholesterol in most HTG patients, serum TG levels need to be lowered below 100 mg/dl. Furthermore, the benefit of gemfibrozil therapy may be significantly enhanced by weight loss during treatment.

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