Facioscapulohumeral Muscular Dystrophy (FSHD) is in the top three list of all dystrophies with an approximate 1:8000 incidence. It is not a life-threatening disease; however, the progression of the disease extends over being wheelchair bound. Despite some drug trials continuing, including DUX4 inhibition, TGF-ß inhibition and resokine which promote healthier muscle, there is not an applicable treatment option for FSHD today. Still, there is a need for new agents to heal, stop or at least slow down muscle wasting. Current FSHD studies involving nutraceuticals as vitamin C, vitamin E, coenzyme Q10, zinc, selenium, and phytochemicals as curcumin or genistein, daidzein flavonoids provide promising treatment strategies. In this review, we present the clinical and molecular nature of FSHD and focus on nutraceuticals and phytochemicals that may alleviate FSHD. In the light of the association of impaired pathophysiological FSHD pathways with nutraceuticals and phytochemicals according to the literature, we present both studied and novel approaches that can contribute to FSHD treatment.
ISSN (dc.identifier.issn) | 1570-159X |
Haklar (dc.rights) | info:eu-repo/semantics/openAccess |
Eser Adı (dc.title) | Promising Perspective to Facioscapulohumeral Muscular Dystrophy Treatment: Nutraceuticals and Phytochemicals. |
Özet (dc.description.abstract) | Facioscapulohumeral Muscular Dystrophy (FSHD) is in the top three list of all dystrophies with an approximate 1:8000 incidence. It is not a life-threatening disease; however, the progression of the disease extends over being wheelchair bound. Despite some drug trials continuing, including DUX4 inhibition, TGF-ß inhibition and resokine which promote healthier muscle, there is not an applicable treatment option for FSHD today. Still, there is a need for new agents to heal, stop or at least slow down muscle wasting. Current FSHD studies involving nutraceuticals as vitamin C, vitamin E, coenzyme Q10, zinc, selenium, and phytochemicals as curcumin or genistein, daidzein flavonoids provide promising treatment strategies. In this review, we present the clinical and molecular nature of FSHD and focus on nutraceuticals and phytochemicals that may alleviate FSHD. In the light of the association of impaired pathophysiological FSHD pathways with nutraceuticals and phytochemicals according to the literature, we present both studied and novel approaches that can contribute to FSHD treatment. |
Yayın Tarihi (dc.date.issued) | 2021 |
Kayıt Giriş Tarihi (dc.date.accessioned) | 2022-03-01T14:10:39Z |
Açık Erişim tarihi (dc.date.available) | 2022-03-01T14:10:39Z |
Yayın Dili (dc.language.iso) | English |
Konu Başlıkları (dc.subject) | FSHD |
Konu Başlıkları (dc.subject) | Facioscapulohumeral muscular dystrophy |
Konu Başlıkları (dc.subject) | dystrophy. |
Konu Başlıkları (dc.subject) | natural compound |
Konu Başlıkları (dc.subject) | nutraceutical |
Konu Başlıkları (dc.subject) | phytochemical |
Konu Başlıkları (dc.subject) | skeletal muscle |
Yayının ilk Sayfa Sayısı (dc.identifier.startpage) | 2276 |
Yayının son sayfa sayısı (dc.identifier.endpage) | 2295 |
Dergi Adı (dc.relation.journal) | CURRENT NEUROPHARMACOLOGY |
Dergi Sayısı (dc.identifier.issue) | 12 |
Dergi Cilt (dc.identifier.volume) | 19 |
Yayın Türü (dc.type) | Makale |
Yazar/lar (dc.contributor.author) | Hangül, Ceren |
Yazar/lar (dc.contributor.author) | Karaüzüm, Sibel Berker |
Yazar/lar (dc.contributor.author) | Akkol, Esra Küpeli |
Yazar/lar (dc.contributor.author) | Demir-Dora, Devrim |
Yazar/lar (dc.contributor.author) | Çetin, Zafer |
Yazar/lar (dc.contributor.author) | Saygılı, Eyüp İlker |
Yazar/lar (dc.contributor.author) | Evcili, Gökhan |
Yazar/lar (dc.contributor.author) | Sobarzo-Sánchez, Eduardo |
Tek Biçim Adres (dc.identifier.uri) | http://hdl.handle.net/handle/20.500.12527/714 |
DOI Numarası (dc.identifier.doi) | 10.2174/1570159X19666210726151924 |
Kurum Yazar/lar (dc.contributor.sankoauthor) | Zafer Çetin |
Kurum Yazar/lar (dc.contributor.sankoauthor) | Eyüp İlker Saygılı |
Atıf Dizini (dc.source.database) | Wos |
Wos Id (dc.identifier.wos) | 000731396800008 |