Statin induced myopathy

Revision as of 20:55, 28 November 2012 by Rim Halaby (talk | contribs)
Jump to navigation Jump to search

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Rim Halaby

Overview

Definition

Statin induced myopathy is a spectrum of muscular problems caused by the intake of statin. Myopathy by definition is the abnormal function of the muscle. The spectrum of statin induced myopathy includes:

Myalgia

  • Myalgia is defined as one or combination of muscle weakness, tenderness or pain.
  • Patients usually complain of cramping feeling in the muscles.
  • Creatine kinase may be normal or minimally elevated.

Asymptomatic increase in creatine kinase

Myositis

  • Myositis is the inflammation of the muscle characterised by muscular complaints in the setting of elevated creatine kinase up to ten folds.

Rhabdomyositis

  • Rhabdomyositis is the acute degeneration of the skeletal muscle.
  • It is a potentially lethal condition due to its associated nephrotoxicity caused by myoglobinuria and myoglobinemia.
  • Creatine kinase is elevated in rhabdomyosistis similarly to myositis.
  • The complications of rhabdomyositis are acute tubular necrosis, hypocalcemia, hyperkalemia, metabolic acidosis, hyperuricemia, DIC and cardiomyopathy.[1]

Other Statin Induced Myopathies

  • Elevated creatine kinase after statin withdrawal[2]
  • Autoimmune myopathy requiring immunosuppressive therapy[3]

Prevalence

The prevalence of statin induced myopathy, described as a spectrum of clinical conditions ranging from myalgia to myositis and rhabdomyolysis, is almost 10-15%[4]

Risk Factors

Pathophysiology

Statin induced myopathy has a complex poorly understood multifactorial pathophysiology. It is postulated that statin induced myopathy is caused by apoptosis of the skeletal muscle cells because of disrupted intracellular calcium signaling and depletion of mevalonate metabolism products, notably isoprenoids.[7]

The following changes are caused by statin:

  • Changes in cholesterol content and alteration of the membrane fluidity of skeletal muscle cells which disrupts their normal function
  • Changes in skeletal muscle cells membrane electrical properties
  • Changes in Na+/K+ pump density resulting in decreased production of ATP
  • Changes in the excitation-contraction coupling
  • Changes in the cell surface receptor transduction cascades
  • Decreased synthesis of ubiquinone (Q10), a component of the mitochondrial electron transport chain, leading to decreased ATP production and decreased free radical scavenging
  • Increased intracellular calcium causing apoptosis of the skeletal muscle cells[1]
  • Decreased mevalonate metabolism products, particularly isoprenoids, leading to a chain of events that culminate in the apoptosis of skeletal muscle cells[7]
Shown below is an image depicting the mechanism of statin induced myopathy through increasing the intracellular calcium concentration.
Statin induced myopathy through increased intracellular calcium
Statin induced myopathy through increased intracellular calcium

Treatment

References

  1. 1.0 1.1 Baker, S.K. & Tarnopolsky, M.A. (2001). Statin myopathies: pathophysiologic and clinical perspectives. Clin. Invest. Med., 24(5): 258-272.
  2. Thompson PD, Clarkson P, Karas RH (2003). "Statin-associated myopathy". JAMA. 289 (13): 1681–90. doi:10.1001/jama.289.13.1681. PMID 12672737.
  3. Radcliffe KA, Campbell WW (2008). "Statin myopathy". Curr Neurol Neurosci Rep. 8 (1): 66–72. PMID 18367041.
  4. 4.0 4.1 4.2 4.3 Harper CR, Jacobson TA (2010). "Evidence-based management of statin myopathy". Curr Atheroscler Rep. 12 (5): 322–30. doi:10.1007/s11883-010-0120-9. PMID 20628837.
  5. 5.0 5.1 5.2 Venero CV, Thompson PD (2009). "Managing statin myopathy". Endocrinol Metab Clin North Am. 38 (1): 121–36. doi:10.1016/j.ecl.2008.11.002. PMID 19217515.
  6. 6.0 6.1 6.2 Hamilton-Craig I (2001). "Statin-associated myopathy". Med J Aust. 175 (9): 486–9. PMID 11758079.
  7. 7.0 7.1 Dirks AJ, Jones KM (2006). "Statin-induced apoptosis and skeletal myopathy". Am J Physiol Cell Physiol. 291 (6): C1208–12. doi:10.1152/ajpcell.00226.2006. PMID 16885396.