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评估他汀类药物治疗患者小腿运动时的骨骼肌:31 磷磁共振波谱分析。

Evaluation of skeletal muscle during calf exercise by 31-phosphorus magnetic resonance spectroscopy in patients on statin medications.

机构信息

Department of Radiology, Beth Israel Deaconess Medical Center, 330 Brookline Avenue, Boston, Massachusetts 02215, USA.

出版信息

Muscle Nerve. 2011 Jan;43(1):76-81. doi: 10.1002/mus.21847.

DOI:10.1002/mus.21847
PMID:21171098
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3332539/
Abstract

Muscle pain is a common side effect of statin medications, but the cause is poorly understood. We characterized phosphocreatine (PCr) exercise recovery kinetics in 10 patients with hypercholesterolemia before and after a 4-week regimen of statin therapy using 31-phosphorus magnetic resonance spectroscopy ((31) P-MRS). (31) P spectra were obtained before, during, and after exercise on a calf flexion pedal ergometer. Creatine kinase (CK) serum levels were drawn before and after statin therapy. The mean metabolic recovery time constant in subjects increased from 28.1 s (SE = 6.5 s) to 55.4 s (SE = 7.4 s) after statin therapy. The unweighted mean of the pre/post-recovery time difference was -27.3 s (SE = 12.4 s; P = 0.02). Pre- and post-therapy CK levels were not significantly different (P = 0.50). Metabolic recovery time in the calf is prolonged in patients after statin use. This suggests that statins impair mitochondrial oxidative function, and (31) P MRS is a potential study model for statin-associated myopathy.

摘要

肌肉疼痛是他汀类药物的常见副作用,但病因尚不清楚。我们使用 31 磷磁共振波谱(31 P-MRS)在 10 名高胆固醇血症患者使用他汀类药物治疗 4 周前后,对其肌肉疼痛的磷酸肌酸(PCr)运动恢复动力学进行了特征描述。(31)P 谱在小腿屈伸脚踏功率计运动前、运动中和运动后获得。在他汀类药物治疗前后抽取肌酸激酶(CK)血清水平。与他汀类药物治疗前相比,受试者的平均代谢恢复时间常数从 28.1 秒(SE=6.5 秒)增加到 55.4 秒(SE=7.4 秒)。恢复前/后时间差的未加权平均值为-27.3 秒(SE=12.4 秒;P=0.02)。治疗前后 CK 水平无显著差异(P=0.50)。他汀类药物使用后,小腿的代谢恢复时间延长。这表明他汀类药物会损害线粒体氧化功能,31 P-MRS 是他汀类药物相关肌病的潜在研究模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f545/3332539/3c62fabe6970/nihms369733f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f545/3332539/ca0354728554/nihms369733f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f545/3332539/4cfae2c7d5ef/nihms369733f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f545/3332539/3c62fabe6970/nihms369733f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f545/3332539/ca0354728554/nihms369733f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f545/3332539/4cfae2c7d5ef/nihms369733f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f545/3332539/3c62fabe6970/nihms369733f3.jpg

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CMAJ. 2009 Jul 7;181(1-2):E11-8. doi: 10.1503/cmaj.081785.
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Statin-induced muscle damage and atrogin-1 induction is the result of a geranylgeranylation defect.他汀类药物诱导的肌肉损伤和肌萎缩相关基因1(atrogin-1)的诱导是香叶基香叶基化缺陷的结果。
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Large-scale chemical dissection of mitochondrial function.线粒体功能的大规模化学剖析
The impact of statin therapy and aerobic exercise training on skeletal muscle and whole-body aerobic capacity.
他汀类药物治疗和有氧运动训练对骨骼肌及全身有氧能力的影响。
Am Heart J Plus. 2021 May;5. doi: 10.1016/j.ahjo.2021.100028. Epub 2021 Jun 24.
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Effects of statins on mitochondrial pathways.他汀类药物对线粒体途径的影响。
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Neurotherapeutics. 2018 Oct;15(4):1006-1017. doi: 10.1007/s13311-018-0670-z.
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Mitochondrial function is impaired in the skeletal muscle of pre-frail elderly.衰弱前期老年人骨骼肌中线粒体功能受损。
Sci Rep. 2018 Jun 4;8(1):8548. doi: 10.1038/s41598-018-26944-x.
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Management of Statin Intolerance in 2018: Still More Questions Than Answers.2018 年他汀类药物不耐受的管理:仍有许多问题有待解答。
Am J Cardiovasc Drugs. 2018 Jun;18(3):157-173. doi: 10.1007/s40256-017-0259-7.
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Skeletal muscle metabolic adaptations to endurance exercise training are attainable in mice with simvastatin treatment.在接受辛伐他汀治疗的小鼠中,骨骼肌对耐力运动训练的代谢适应性是可以实现的。
PLoS One. 2017 Feb 16;12(2):e0172551. doi: 10.1371/journal.pone.0172551. eCollection 2017.
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Non-invasive assessment of phosphate metabolism and oxidative capacity in working skeletal muscle in healthy young Chinese volunteers using (31)P Magnetic Resonance Spectroscopy.使用磷-31磁共振波谱对健康中国年轻志愿者工作状态下骨骼肌的磷代谢和氧化能力进行无创评估。
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The muscle-specific ubiquitin ligase atrogin-1/MAFbx mediates statin-induced muscle toxicity.肌肉特异性泛素连接酶atrogin-1/MAFbx介导他汀类药物诱导的肌肉毒性。
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