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降脂药物的致癌性。

Carcinogenicity of lipid-lowering drugs.

作者信息

Newman T B, Hulley S B

机构信息

Department of Laboratory Medicine, School of Medicine, University of California, San Francisco, USA.

出版信息

JAMA. 1996 Jan 3;275(1):55-60.

PMID:8531288
Abstract

OBJECTIVE

To review the findings and implications of studies of rodent carcinogenicity of lipid-lowering drugs.

DATA SOURCES

Summaries of carcinogenicity studies published in the 1992 and 1994 Physicians' Desk Reference (PDR), additional information obtained from the US Food and Drug Administration, and published articles identified by computer searching, bibliographies, and consultation with experts.

STUDY SAMPLE

We tabulated rodent carcinogenicity data from the 1994 PDR for all drugs listed as "hypolipidemics." For comparison, we selected a stratified random sample of antihypertensive drugs. We also reviewed methods and interpretation of carcinogenicity studies in rodents and results of clinical trials in humans.

DATA SYNTHESIS

All members of the two most popular classes of lipid-lowering drugs (the fibrates and the statins) cause cancer in rodents, in some cases at levels of animal exposure close to those prescribed to humans. In contrast, few of the antihypertensive drugs have been found to be carcinogenic in rodents. Evidence of carcinogenicity of lipid-lowering drugs from clinical trials in humans is inconclusive because of inconsistent results and insufficient duration of follow-up.

CONCLUSIONS

Extrapolation of this evidence of carcinogenesis from rodents to humans is an uncertain process. Longer-term clinical trials and careful postmarketing surveillance during the next several decades are needed to determine whether cholesterol-lowering drugs cause cancer in humans. In the meantime, the results of experiments in animals and humans suggest that lipid-lowering drug treatment, especially with the fibrates and statins, should be avoided except in patients at high short-term risk of coronary heart disease.

摘要

目的

回顾关于降脂药物啮齿动物致癌性研究的结果及意义。

数据来源

1992年和1994年《医师案头参考》(PDR)中发表的致癌性研究摘要、从美国食品药品监督管理局获得的其他信息,以及通过计算机检索、参考文献和专家咨询确定的已发表文章。

研究样本

我们将1994年PDR中列为“降血脂药”的所有药物的啮齿动物致癌性数据制成表格。为作比较,我们选取了分层随机抽样的抗高血压药物。我们还回顾了啮齿动物致癌性研究的方法及解读以及人类临床试验的结果。

数据综合

两类最常用的降脂药物(贝特类药物和他汀类药物)中的所有药物都会在啮齿动物中引发癌症,在某些情况下,动物接触药物的水平接近人类的用药剂量。相比之下,很少有抗高血压药物被发现对啮齿动物具有致癌性。由于结果不一致且随访时间不足,降脂药物在人类临床试验中的致癌性证据尚无定论。

结论

将这种致癌性证据从啮齿动物外推至人类是一个不确定的过程。需要进行更长期的临床试验以及在未来几十年进行仔细的上市后监测,以确定降胆固醇药物是否会在人类中引发癌症。与此同时,动物和人类实验的结果表明,除了冠心病短期风险高的患者外,应避免使用降脂药物治疗,尤其是贝特类药物和他汀类药物。

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