Step-by-step diagnosis and management of the nocebo/drucebo effect in statin-associated muscle symptoms patients: a position paper from the International Lipid Expert Panel (ILEP).
Peter E PensonEric BruckertDavid MaraisŽeljko ReinerMatteo PirroAmirhossein SahebkarGani BajraktariErkin MirrakhimovManfredi RizzoDimitri P MikhailidisAlexandros SachinidisDan GaitaGustavs LatkovskisMohsen MazidiPeter P TothDaniel PellaFahad AlnouriArman PostadzhiyanHung-I YehG B John ManciniStephan von HaehlingMaciej Banachnull nullPublished in: Journal of cachexia, sarcopenia and muscle (2022)
Statin intolerance is a clinical syndrome whereby adverse effects (AEs) associated with statin therapy [most commonly statin-associated muscle symptoms (SAMS)] result in the discontinuation of therapy and consequently increase the risk of adverse cardiovascular outcomes. However, complete statin intolerance occurs in only a small minority of treated patients (estimated prevalence of only 3-5%). Many perceived AEs are misattributed (e.g. physical musculoskeletal injury and inflammatory myopathies), and subjective symptoms occur as a result of the fact that patients expect them to do so when taking medicines (the nocebo/drucebo effect)-what might be truth even for over 50% of all patients with muscle weakness/pain. Clear guidance is necessary to enable the optimal management of plasma in real-world clinical practice in patients who experience subjective AEs. In this Position Paper of the International Lipid Expert Panel (ILEP), we present a step-by-step patient-centred approach to the identification and management of SAMS with a particular focus on strategies to prevent and manage the nocebo/drucebo effect and to improve long-term compliance with lipid-lowering therapy.
Keyphrases
- end stage renal disease
- newly diagnosed
- ejection fraction
- cardiovascular disease
- clinical practice
- coronary artery disease
- chronic kidney disease
- mental health
- skeletal muscle
- peritoneal dialysis
- prognostic factors
- stem cells
- oxidative stress
- risk factors
- sleep quality
- neuropathic pain
- spinal cord
- fatty acid
- mesenchymal stem cells
- bone marrow
- social support
- cell therapy