Circulatory 25(OH)D and 1,25(OH)

1,25(OH)2D, 1,25-dihydroxyvitamin D3 (Calcitriol) 25(OH)D, 25-hydroxyvitamin D3 H&Y, Hoehn &Yahr rating scale Hoehn & Yahr staging scale MMSE, Mini mental state examination MSA, Multiple system atrophy MoCA, Montreal Cognitive Assessment Multiple system atrophy PD, Parkinson's disease Parkinson's disease UMSARS, Unified MSA Rating Scale UPDRS, Unified PD Rating Scale. Unified MSA rating scale Unified PD rating scale Vitamin D

Journal

eNeurologicalSci
ISSN: 2405-6502
Titre abrégé: eNeurologicalSci
Pays: Netherlands
ID NLM: 101667077

Informations de publication

Date de publication:
Dec 2021
Historique:
received: 24 05 2021
revised: 24 08 2021
accepted: 17 09 2021
entrez: 6 10 2021
pubmed: 7 10 2021
medline: 7 10 2021
Statut: epublish

Résumé

There is sufficient evidence to support vitamin D's noncalcemic effects and the role of vitamin D deficiency in the development of a wide range of neurological disorders. This study aimed to evaluate whether serum 25(OH)D and 1,25(OH) 2 D could be used as biomarkers to differentiate between healthy subjects (HS), multiple system atrophy (MSA) and Parkinson's disease (PD) patients of both genders. A total of 107 subjects were included in this study, divided into three groups: 1- HS ( The levels of 25(OH)D and 1,25(OH) 2 D in HS were 26.85 +/- 7.62 ng/mL and 53.63 +/- 13.66 pg/mL respectively. 25(OH)D levels were lower in both MSA and PD by 61% and 50%, respectively ( Serum 25(OH)D and 1,25(OH) 2 D could be useful biomarkers for MSA and PD. 25(OH)D and H&Y provided the highest sensitivity and group classification characteristics.

Sections du résumé

BACKGROUND AND PURPOSE OBJECTIVE
There is sufficient evidence to support vitamin D's noncalcemic effects and the role of vitamin D deficiency in the development of a wide range of neurological disorders. This study aimed to evaluate whether serum 25(OH)D and 1,25(OH) 2 D could be used as biomarkers to differentiate between healthy subjects (HS), multiple system atrophy (MSA) and Parkinson's disease (PD) patients of both genders.
METHODS METHODS
A total of 107 subjects were included in this study, divided into three groups: 1- HS (
RESULTS RESULTS
The levels of 25(OH)D and 1,25(OH) 2 D in HS were 26.85 +/- 7.62 ng/mL and 53.63 +/- 13.66 pg/mL respectively. 25(OH)D levels were lower in both MSA and PD by 61% and 50%, respectively (
CONCLUSIONS CONCLUSIONS
Serum 25(OH)D and 1,25(OH) 2 D could be useful biomarkers for MSA and PD. 25(OH)D and H&Y provided the highest sensitivity and group classification characteristics.

Identifiants

pubmed: 34611554
doi: 10.1016/j.ensci.2021.100369
pii: S2405-6502(21)00061-7
pmc: PMC8477135
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100369

Informations de copyright

© 2021 The Author(s).

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Auteurs

Hiromu Ogura (H)

Department of Neurology, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.

Izzettin Hatip-Al-Khatib (I)

Department of Medical Pharmacology, Faculty of Medicine, Pamukkale University, Denizli, Turkey.

Midori Suenaga (M)

Department of Medical Pharmacology, Faculty of Pharmaceutical Sciences, Tokushima-Bunri University, Tokushima, Japan.

Funda Bolukbasi Hatip (FB)

Department of Medical Pharmacology, Faculty of Medicine, Pamukkale University, Denizli, Turkey.

Takayasu Mishima (T)

Department of Neurology, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.

Shinsuke Fujioka (S)

Department of Neurology, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.

Shinji Ouma (S)

Department of Neurology, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.

Yoichi Matsunaga (Y)

Department of Neurology, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.

Yoshio Tsuboi (Y)

Department of Neurology, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.

Classifications MeSH