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肌氨酸合成减少能否预防他汀类药物肌病?

Does reduced creatine synthesis protect against statin myopathy?

机构信息

Division of Cardiology, Henry Low Heart Center, Hartford Hospital, Hartford, CT 06102, USA.

出版信息

Cell Metab. 2013 Dec 3;18(6):773-4. doi: 10.1016/j.cmet.2013.11.012.

DOI:10.1016/j.cmet.2013.11.012
PMID:24315367
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3899594/
Abstract

Statins, widely used to lower cholesterol levels, cause myopathy in some patients. Mangravite et al. (2013) show that a single nucleotide polymorphism decreasing expression of glycine amidinotransferase (GATM), the enzyme regulating creatine biosynthesis, is associated with reduced statin myopathy. Whether reduced creatine production protects against statin myopathy remains to be determined.

摘要

他汀类药物广泛用于降低胆固醇水平,但会导致部分患者出现肌肉疾病。Mangravite 等人(2013 年)表明,降低甘氨酸脒基转移酶(GATM)表达的单核苷酸多态性与他汀类药物引起的肌肉疾病减少有关,GATM 是调节肌酸生物合成的酶。减少肌酸生成是否能预防他汀类药物引起的肌肉疾病仍有待确定。

相似文献

1
Does reduced creatine synthesis protect against statin myopathy?肌氨酸合成减少能否预防他汀类药物肌病?
Cell Metab. 2013 Dec 3;18(6):773-4. doi: 10.1016/j.cmet.2013.11.012.
2
GATM gene variants and statin myopathy risk.GATM基因变异与他汀类药物性肌病风险
Nature. 2014 Sep 18;513(7518):E1. doi: 10.1038/nature13628.
3
A statin-dependent QTL for GATM expression is associated with statin-induced myopathy.一个依赖于他汀类药物的 GATM 表达的 QTL 与他汀类药物诱导的肌病有关。
Nature. 2013 Oct 17;502(7471):377-80. doi: 10.1038/nature12508. Epub 2013 Aug 28.
4
Mangravite et al. reply.曼格拉维特等人回复。
Nature. 2014 Sep 18;513(7518):E3. doi: 10.1038/nature13630.
5
Expression quantitative trait locus analysis identifies novel genes for statin myopathy.表达数量性状基因座分析确定了他汀类药物肌病的新基因。
Circ Cardiovasc Genet. 2014 Apr;7(2):220-1. doi: 10.1161/CIRCGENETICS.114.000611.
6
GATM locus does not replicate in rhabdomyolysis study.GATM基因座在横纹肌溶解症研究中未出现复制情况。
Nature. 2014 Sep 18;513(7518):E1-3. doi: 10.1038/nature13629.
7
The association of GATM polymorphism with statin-induced myopathy: a systematic review and meta-analysis.GATM 多态性与他汀类药物诱导的肌病的关联:系统评价和荟萃分析。
Eur J Clin Pharmacol. 2021 Mar;77(3):349-357. doi: 10.1007/s00228-020-03019-3. Epub 2020 Oct 13.
8
GATM polymorphism associated with the risk for statin-induced myopathy does not replicate in case-control analysis of 715 dyslipidemic individuals.与他汀类药物引起的肌病风险相关的GATM基因多态性在715名血脂异常个体的病例对照分析中未得到重复验证。
Cell Metab. 2015 Apr 7;21(4):622-7. doi: 10.1016/j.cmet.2015.03.003.
9
Correlation between single-nucleotide polymorphisms and statin-induced myopathy: a mixed-effects model meta-analysis.单核苷酸多态性与他汀类药物诱导的肌病的相关性:混合效应模型荟萃分析。
Eur J Clin Pharmacol. 2021 Apr;77(4):569-581. doi: 10.1007/s00228-020-03029-1. Epub 2020 Nov 4.
10
Genetic factors affecting statin concentrations and subsequent myopathy: a HuGENet systematic review.影响他汀类药物浓度及后续肌病的遗传因素:一项HuGENet系统评价
Genet Med. 2014 Nov;16(11):810-9. doi: 10.1038/gim.2014.41. Epub 2014 May 8.

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Anim Nutr. 2021 Dec;7(4):1271-1282. doi: 10.1016/j.aninu.2021.06.014. Epub 2021 Sep 30.
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Effects of statins on mitochondrial pathways.他汀类药物对线粒体途径的影响。
J Cachexia Sarcopenia Muscle. 2021 Apr;12(2):237-251. doi: 10.1002/jcsm.12654. Epub 2021 Jan 29.
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The association of GATM polymorphism with statin-induced myopathy: a systematic review and meta-analysis.

本文引用的文献

1
A statin-dependent QTL for GATM expression is associated with statin-induced myopathy.一个依赖于他汀类药物的 GATM 表达的 QTL 与他汀类药物诱导的肌病有关。
Nature. 2013 Oct 17;502(7471):377-80. doi: 10.1038/nature12508. Epub 2013 Aug 28.
2
Statin-associated autoimmune myopathy and anti-HMGCR autoantibodies.他汀类药物相关性自身免疫性肌病与抗 HMGCR 自身抗体。
Muscle Nerve. 2013 Oct;48(4):477-83. doi: 10.1002/mus.23854. Epub 2013 Aug 30.
3
Effect of statins on skeletal muscle function.他汀类药物对骨骼肌功能的影响。
GATM 多态性与他汀类药物诱导的肌病的关联:系统评价和荟萃分析。
Eur J Clin Pharmacol. 2021 Mar;77(3):349-357. doi: 10.1007/s00228-020-03019-3. Epub 2020 Oct 13.
4
The adjuvant value of Herba Cistanches when used in combination with statin in murine models.肉苁蓉在与他汀类药物联合使用时的佐剂价值。
Sci Rep. 2017 Aug 24;7(1):9391. doi: 10.1038/s41598-017-10008-7.
5
GATM polymorphism associated with the risk for statin-induced myopathy does not replicate in case-control analysis of 715 dyslipidemic individuals.与他汀类药物引起的肌病风险相关的GATM基因多态性在715名血脂异常个体的病例对照分析中未得到重复验证。
Cell Metab. 2015 Apr 7;21(4):622-7. doi: 10.1016/j.cmet.2015.03.003.
6
Combining genetic and nongenetic biomarkers to realize the promise of pharmacogenomics for inflammatory diseases.结合遗传和非遗传生物标志物,以实现药物基因组学在炎症性疾病方面的前景。
Pharmacogenomics. 2014;15(15):1931-40. doi: 10.2217/pgs.14.129.
7
Mechanisms and assessment of statin-related muscular adverse effects.他汀类药物相关肌肉不良反应的机制与评估
Br J Clin Pharmacol. 2014 Sep;78(3):454-66. doi: 10.1111/bcp.12360.
8
Genetic factors affecting statin concentrations and subsequent myopathy: a HuGENet systematic review.影响他汀类药物浓度及后续肌病的遗传因素:一项HuGENet系统评价
Genet Med. 2014 Nov;16(11):810-9. doi: 10.1038/gim.2014.41. Epub 2014 May 8.
Circulation. 2013 Jan 1;127(1):96-103. doi: 10.1161/CIRCULATIONAHA.112.136101. Epub 2012 Nov 26.
4
Mechanisms of statin-induced myalgia assessed by physiogenomic associations.通过生理基因组关联评估他汀类药物引起的肌肉疼痛的机制。
Atherosclerosis. 2011 Oct;218(2):451-6. doi: 10.1016/j.atherosclerosis.2011.07.007. Epub 2011 Jul 20.
5
Creatine supplementation prevents statin-induced muscle toxicity.补充肌酸可预防他汀类药物引起的肌肉毒性。
Ann Intern Med. 2010 Nov 16;153(10):690-2. doi: 10.7326/0003-4819-153-10-201011160-00024.
6
l-arginine:glycine amidinotransferase (AGAT) deficiency: clinical presentation and response to treatment in two patients with a novel mutation.精氨酸-甘氨酸 amidinotransferase(AGAT)缺陷:两例新型突变患者的临床表现和治疗反应。
Mol Genet Metab. 2010 Oct-Nov;101(2-3):228-32. doi: 10.1016/j.ymgme.2010.06.021. Epub 2010 Jul 7.
7
The genetics of statin-induced myopathy.他汀类药物引起的肌病的遗传学。
Atherosclerosis. 2010 Jun;210(2):337-43. doi: 10.1016/j.atherosclerosis.2009.11.033. Epub 2009 Nov 27.
8
The SLCO1B1*5 genetic variant is associated with statin-induced side effects.SLCO1B1*5基因变异与他汀类药物引起的副作用相关。
J Am Coll Cardiol. 2009 Oct 20;54(17):1609-16. doi: 10.1016/j.jacc.2009.04.053.
9
Use of an electronic medical record to characterize cases of intermediate statin-induced muscle toxicity.利用电子病历对他汀类药物所致中度肌肉毒性病例进行特征分析。
Prev Cardiol. 2009 Spring;12(2):88-94. doi: 10.1111/j.1751-7141.2009.00028.x.
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SLCO1B1 variants and statin-induced myopathy--a genomewide study.溶质载体有机阴离子转运体家族1成员B1(SLCO1B1)变异与他汀类药物诱发的肌病——一项全基因组研究
N Engl J Med. 2008 Aug 21;359(8):789-99. doi: 10.1056/NEJMoa0801936. Epub 2008 Jul 23.