Expression Analysis of VDR-Related LncRNAs in Autism Spectrum Disorder.


Journal

Journal of molecular neuroscience : MN
ISSN: 1559-1166
Titre abrégé: J Mol Neurosci
Pays: United States
ID NLM: 9002991

Informations de publication

Date de publication:
Jul 2021
Historique:
received: 05 04 2021
accepted: 10 05 2021
pubmed: 15 6 2021
medline: 13 1 2022
entrez: 14 6 2021
Statut: ppublish

Résumé

Vitamin D receptor (VDR) signaling has been reported to affect neurodevelopment, thus participating in the risk of autism spectrum disorder (ASD). We have measured expression amounts of VDR, CYP27B1, and two related long non-coding RNAs, namely SNHG6 and LINC00511, in the circulation of ASD patients compared with normal controls. Expression of CYP27B1 was remarkably higher in ASD cases compared with controls (posterior beta = 2.38, SE = 0.46, adjusted P value < 0.0001, 95% credible interval (CrI) for beta = [1.49, 3.27]). Level of SNHG6 was lower in ASD cases compared with controls (posterior beta = - 0.791, SE = 0.24, adjusted P value = 0.029, 95% CrI for beta = [- 1.27, - 0.33]). Expression levels of VDR and LINC00511 were similar between ASD cases and controls (P values = 0.97 and 0.46, respectively). Expressions of VDR, CYP27B1, SNHG6, and LINC00511 were not correlated with age of children. However, significant correlations were perceived between expressions of CYP27B1 and LINC00511 (r = 0.47, P < 0.0001), VDR and CYP27B1 (r = 0.42, P < 0.0001), and VDR and SNHG6 (r = 0.32, P < 0.0001). Therefore, these results imply dysregulation of a number of VDR-related genes in ASD patients.

Identifiants

pubmed: 34125396
doi: 10.1007/s12031-021-01858-y
pii: 10.1007/s12031-021-01858-y
doi:

Substances chimiques

RNA, Long Noncoding 0
Receptors, Calcitriol 0
VDR protein, human 0
long non-coding RNA SNHG6, human 0
25-Hydroxyvitamin D3 1-alpha-Hydroxylase EC 1.14.15.18
CYP27B1 protein, human EC 1.14.15.18

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1403-1409

Références

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Auteurs

Soudeh Ghafouri-Fard (S)

Department of Medical Genetics, School of Medicine Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Reyhane Eghtedarian (R)

Department of Medical Genetics, School of Medicine Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Bashdar Mahmud Hussen (BM)

Department of Pharmacognosy, College of Pharmacy, Hawler Medical University, Erbil, Iraq.

Elahe Motevaseli (E)

Department of Molecular Medicine, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.

Shahram Arsang-Jang (S)

Cancer Gene Therapy Research Center, Zanjan University of Medical Science, Zanjan, Iran.

Mohammad Taheri (M)

Skull Base Research Center, Loghman Hakim Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran. mohammad_823@yahoo.com.

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