A phase Ib/IIa clinical trial of dantrolene sodium in patients with Wolfram syndrome.
Adolescent
Adult
Biological Availability
Calcium Signaling
/ drug effects
Child
Dantrolene
/ administration & dosage
Dose-Response Relationship, Drug
Drug Monitoring
/ methods
Humans
Insulin-Secreting Cells
/ drug effects
Interleukin-18
/ analysis
Interleukin-1beta
/ analysis
Molecular Targeted Therapy
/ methods
Muscle Relaxants, Central
/ administration & dosage
Neurologic Examination
/ drug effects
Quality of Life
Treatment Outcome
Visual Acuity
/ drug effects
Wolfram Syndrome
/ diagnosis
Cell stress
Diabetes
Endocrinology
Genetic diseases
Genetics
Journal
JCI insight
ISSN: 2379-3708
Titre abrégé: JCI Insight
Pays: United States
ID NLM: 101676073
Informations de publication
Date de publication:
09 08 2021
09 08 2021
Historique:
received:
15
10
2020
accepted:
18
06
2021
pubmed:
30
6
2021
medline:
26
2
2022
entrez:
29
6
2021
Statut:
epublish
Résumé
BACKGROUNDWolfram syndrome is a rare ER disorder characterized by insulin-dependent diabetes mellitus, optic nerve atrophy, and progressive neurodegeneration. Although there is no treatment for Wolfram syndrome, preclinical studies in cell and rodent models suggest that therapeutic strategies targeting ER calcium homeostasis, including dantrolene sodium, may be beneficial.METHODSBased on results from preclinical studies on dantrolene sodium and ongoing longitudinal studies, we assembled what we believe is the first-ever clinical trial in pediatric and adult Wolfram syndrome patients with an open-label phase Ib/IIa trial design. The primary objective was to assess the safety and tolerability of dantrolene sodium in adult and pediatric Wolfram syndrome patients. Secondary objectives were to evaluate the efficacy of dantrolene sodium on residual pancreatic β cell functions, visual acuity, quality-of-life measures related to vision, and neurological functions.RESULTSDantrolene sodium was well tolerated by Wolfram syndrome patients. Overall, β cell functions were not significantly improved, but there was a significant correlation between baseline β cell functions and change in β cell responsiveness (R2, P = 0.004) after 6-month dantrolene therapy. Visual acuity and neurological functions were not improved by 6-month dantrolene sodium. Markers of inflammatory cytokines and oxidative stress, such as IFN-γ, IL-1β, TNF-α, and isoprostane, were elevated in subjects.CONCLUSIONThis study justifies further investigation into using dantrolene sodium and other small molecules targeting the ER for treatment of Wolfram syndrome.TRIAL REGISTRATIONClinicalTrials.gov identifier NCT02829268FUNDINGNIH/National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) (DK112921, DK113487, DK020579), NIH/National Center for Advancing Translational Sciences (NCATS) (TR002065, TR000448), NIH training grant (F30DK111070), Silberman Fund, Ellie White Foundation, Snow Foundation, Unravel Wolfram Syndrome Fund, Stowe Fund, Eye Hope Foundation, Feiock Fund, Washington University Institute of Clinical and Translational Sciences grant UL1TR002345 from NIH/NCATS, Bursky Center for Human Immunology & Immunotherapy Programs.
Identifiants
pubmed: 34185708
pii: e145188
doi: 10.1172/jci.insight.145188
pmc: PMC8410026
doi:
pii:
Substances chimiques
Interleukin-18
0
Interleukin-1beta
0
Muscle Relaxants, Central
0
Dantrolene
F64QU97QCR
Banques de données
ClinicalTrials.gov
['NCT02829268']
Types de publication
Clinical Trial, Phase I
Clinical Trial, Phase II
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : NCATS NIH HHS
ID : UH3 TR002065
Pays : United States
Organisme : NIDDK NIH HHS
ID : R21 DK113487
Pays : United States
Organisme : NIDDK NIH HHS
ID : F30 DK111070
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR000448
Pays : United States
Organisme : NIDDK NIH HHS
ID : P60 DK020579
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK020579
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK112921
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR002345
Pays : United States
Organisme : NCATS NIH HHS
ID : UH2 TR002065
Pays : United States
Références
J Clin Invest. 2010 Mar;120(3):744-55
pubmed: 20160352
Diabet Med. 2019 Sep;36(9):1092-1099
pubmed: 30955221
Lab Invest. 2020 Jun;100(6):849-862
pubmed: 32060407
Arch Ophthalmol. 2001 May;119(5):733-40
pubmed: 11346401
Pain. 1987 Jan;28(1):27-38
pubmed: 3822493
PLoS One. 2012;7(7):e40604
pubmed: 22792385
Methods Enzymol. 2007;433:113-26
pubmed: 17954231
Spine (Phila Pa 1976). 2000 Dec 15;25(24):3130-9
pubmed: 11124729
Diabetes. 2014 Mar;63(3):844-6
pubmed: 24556864
J Gen Physiol. 2001 Oct;118(4):355-75
pubmed: 11585849
Curr Diab Rep. 2016 Jan;16(1):6
pubmed: 26742931
J Neurosci. 2009 Jul 22;29(29):9148-62
pubmed: 19625506
J Pediatr. 2013 May;162(5):924-9
pubmed: 23290511
Drugs Future. 2009 Dec;34(12):
pubmed: 26023252
Diabetes Res Clin Pract. 2006 Jun;72(3):298-301
pubmed: 16325298
J AAPOS. 2014 Oct;18(5):461-465.e1
pubmed: 25439303
Adv Biomed Res. 2017 Jul 14;6:83
pubmed: 28808649
Trends Pharmacol Sci. 2019 Oct;40(10):711-714
pubmed: 31420094
Diabetes Care. 2015 Feb;38(2):323-8
pubmed: 25519449
Mult Scler. 2016 Oct;22(11):1386-1396
pubmed: 27207462
J Pharm Sci. 1973 Jun;62(6):948-51
pubmed: 4712630
Cell Metab. 2012 Aug 8;16(2):265-73
pubmed: 22883234
J Alzheimers Dis Parkinsonism. 2017 Aug;7(5):
pubmed: 29214114
Lancet. 1995 Dec 2;346(8988):1458-63
pubmed: 7490992
Nat Genet. 1998 Oct;20(2):143-8
pubmed: 9771706
Biochemistry. 2001 Jan 16;40(2):531-42
pubmed: 11148048
Antioxid Redox Signal. 2007 Dec;9(12):2277-93
pubmed: 17979528
Proc Natl Acad Sci U S A. 2014 Dec 9;111(49):E5292-301
pubmed: 25422446
JAMA Netw Open. 2020 Mar 2;3(3):e201965
pubmed: 32202640
Mol Neurodegener. 2011 Nov 25;6:81
pubmed: 22118545
FEBS Lett. 2006 Oct 16;580(24):5635-40
pubmed: 16989814
Hum Mol Genet. 2021 Apr 26;30(3-4):265-276
pubmed: 33693650
J Biol Chem. 1997 Oct 24;272(43):26965-71
pubmed: 9341133
J Diabetes Complications. 2021 Jan;35(1):107618
pubmed: 32518033
Biomark Insights. 2021 Mar 30;16:11772719211006666
pubmed: 33854293
J R Soc Med. 1986 May;79(5):277-81
pubmed: 3723521
Endocrinology. 2014 Mar;155(3):758-68
pubmed: 24424032
Free Radic Biol Med. 2013 Jun;59:36-44
pubmed: 23044261
Orphanet J Rare Dis. 2012 Nov 14;7:89
pubmed: 23148655
Orphanet J Rare Dis. 2013 Apr 27;8:64
pubmed: 23981289
Nat Protoc. 2007;2(1):221-6
pubmed: 17401357
Sci Rep. 2016 Feb 18;6:21167
pubmed: 26888576
CNS Neurol Disord Drug Targets. 2019;18(9):668-676
pubmed: 29921212