Safety issues and harmful pharmacological interactions of nutritional supplements in Duchenne muscular dystrophy: considerations for Standard of Care and emerging virus outbreaks. (August 2020)
- Record Type:
- Journal Article
- Title:
- Safety issues and harmful pharmacological interactions of nutritional supplements in Duchenne muscular dystrophy: considerations for Standard of Care and emerging virus outbreaks. (August 2020)
- Main Title:
- Safety issues and harmful pharmacological interactions of nutritional supplements in Duchenne muscular dystrophy: considerations for Standard of Care and emerging virus outbreaks
- Authors:
- Boccanegra, Brigida
Verhaart, Ingrid E.C.
Cappellari, Ornella
Vroom, Elizabeth
De Luca, Annamaria - Abstract:
- Graphical abstract: Abstract: At the moment, little treatment options are available for Duchenne muscular dystrophy (DMD). The absence of the dystrophin protein leads to a complex cascade of pathogenic events in myofibres, including chronic inflammation and oxidative stress as well as altered metabolism. The attention towards dietary supplements in DMD is rapidly increasing, with the aim to counteract pathology-related alteration in nutrient intake, the consequences of catabolic distress or to enhance the immunological response of patients as nowadays for the COVID-19 pandemic emergency. By definition, supplements do not exert therapeutic actions, although a great confusion may arise in daily life by the improper distinction between supplements and therapeutic compounds. For most supplements, little research has been done and little evidence is available concerning their effects in DMD as well as their preventing actions against infections. Often these are not prescribed by clinicians and patients/caregivers do not discuss the use with their clinical team. Then, little is known about the real extent of supplement use in DMD patients. It is mistakenly assumed that, since compounds are of natural origin, if a supplement is not effective, it will also do no harm. However, supplements can have serious side effects and also have harmful interactions, in terms of reducing efficacy or leading to toxicity, with other therapies. It is therefore pivotal to shed light on this unclearGraphical abstract: Abstract: At the moment, little treatment options are available for Duchenne muscular dystrophy (DMD). The absence of the dystrophin protein leads to a complex cascade of pathogenic events in myofibres, including chronic inflammation and oxidative stress as well as altered metabolism. The attention towards dietary supplements in DMD is rapidly increasing, with the aim to counteract pathology-related alteration in nutrient intake, the consequences of catabolic distress or to enhance the immunological response of patients as nowadays for the COVID-19 pandemic emergency. By definition, supplements do not exert therapeutic actions, although a great confusion may arise in daily life by the improper distinction between supplements and therapeutic compounds. For most supplements, little research has been done and little evidence is available concerning their effects in DMD as well as their preventing actions against infections. Often these are not prescribed by clinicians and patients/caregivers do not discuss the use with their clinical team. Then, little is known about the real extent of supplement use in DMD patients. It is mistakenly assumed that, since compounds are of natural origin, if a supplement is not effective, it will also do no harm. However, supplements can have serious side effects and also have harmful interactions, in terms of reducing efficacy or leading to toxicity, with other therapies. It is therefore pivotal to shed light on this unclear scenario for the sake of patients. This review discusses the supplements mostly used by DMD patients, focusing on their potential toxicity, due to a variety of mechanisms including pharmacodynamic or pharmacokinetic interactions and contaminations, as well as on reports of adverse events. This overview underlines the need for caution in uncontrolled use of dietary supplements in fragile populations such as DMD patients. A culture of appropriate use has to be implemented between clinicians and patients' groups. … (more)
- Is Part Of:
- Pharmacological research. Volume 158(2020)
- Journal:
- Pharmacological research
- Issue:
- Volume 158(2020)
- Issue Display:
- Volume 158, Issue 2020 (2020)
- Year:
- 2020
- Volume:
- 158
- Issue:
- 2020
- Issue Sort Value:
- 2020-0158-2020-0000
- Page Start:
- Page End:
- Publication Date:
- 2020-08
- Subjects:
- ADME administration distribution, metabolism and elimination -- ADR adverse drug reaction -- ASO antisense oligonucleotide -- BCAA branched-chain amino acid -- CoQ10 Coenzyme Q10 -- CYP cytochrome P450 -- DMD Duchenne muscular dystrophy -- EAA essential amino acid -- EGCG Epigallocatechin-3-gallate -- EMA European Medicines Agency -- EMS Eosinophilia-Myalgia Syndrome -- FDA Food and Drug Administration -- GTE green tea extract -- NAC N-acetyl cysteine -- NO nitric oxide -- NSAID nonsteroidal anti-inflammatory drug -- PD pharmacodynamics -- PK pharmacokinetics -- PUFA polyunsaturated fatty acid -- ROS reactive oxygen species
Duchenne muscular dystrophy -- Dietary supplements -- Adverse drug reactions -- Safety -- COVID-19 -- SARS-CoV-2
Pharmacology -- Periodicals
Pharmacology -- Periodicals
Research -- Periodicals
Médicaments -- Recherche -- Périodiques
Pharmacologie -- Périodiques
615.105 - Journal URLs:
- http://www.sciencedirect.com/science/journal/10436618 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.phrs.2020.104917 ↗
- Languages:
- English
- ISSNs:
- 1043-6618
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6446.550000
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