Calcitriol Treatment Is Safe and Increases Frataxin Levels in Friedreich Ataxia Patients

被引:1
|
作者
Alemany-Perna, Berta [1 ,2 ,3 ,5 ]
Tamarit, Jordi [4 ]
Cabiscol, Elisa [4 ]
Delaspre, Fabien [4 ]
Miguela, Albert [3 ]
Huertas-Pons, Joana Maria [3 ]
Quiroga-Varela, Ana [3 ]
Merchan Ruiz, Miguel [3 ]
Lopez Dominguez, Daniel [1 ,2 ,3 ]
Torrenta, Lluis [2 ]
Genis, David [3 ]
Ros, Joaquim [4 ]
机构
[1] Hosp Josep Trueta, Hosp St Caterina, Neurol Serv, Ataxia Unit,ICS IAS, Girona Salt, Spain
[2] Univ Girona UdG, Dept Med Sci, Girona, Spain
[3] Inst Invest Biomed Girona IDIBGI, Neurodegenerat & Neuroinflammac Grp, Girona, Spain
[4] Univ Lleida, Inst Recerca Biomed Lleida IRBLleida, Dept Ciencies Med Bas, Lleida, Spain
[5] Hosp Univ Josep Trueta, Neurol Serv, Floor 7B,Avinguda Franca S-N, Girona 17007, Spain
关键词
Friedreich ataxia; calcitriol; ataxia; vitamin D; frataxin; CLINICAL-FEATURES; SAMPLE-SIZE; IN-VIVO; PILOT; IMMUNOASSAY; PROGRESSION; MUTATIONS; PROTEIN; TRIAL;
D O I
10.1002/mds.29808
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BackgroundCalcitriol, the active form of vitamin D (also known as 1,25-dihydroxycholecalciferol), improves the phenotype and increases frataxin levels in cell models of Friedreich ataxia (FRDA).ObjectivesBased on these results, we aimed measuring the effects of a calcitriol dose of 0.25 mcg/24h in the neurological function and frataxin levels when administered to FRDA patients for a year.Methods20 FRDA patients where recluted and 15 patients completed the treatment for a year. Evaluations of neurological function changes (SARA scale, 9-HPT, 8-MWT, PATA test) and quality of life (Barthel Scale and Short Form (36) Health Survey [SF-36] quality of life questionnaire) were performed. Frataxin amounts were measured in isolated platelets obtained from these FRDA patients, from heterozygous FRDA carriers (relatives of the FA patients) and from non-heterozygous sex and age matched controls.ResultsAlthough the patients did not experience any observable neurological improvement, there was a statistically significant increase in frataxin levels from initial values, 5.5 to 7.0 pg/mu g after 12 months. Differences in frataxin levels referred to total protein levels were observed among sex- and age-matched controls (18.1 pg/mu g), relative controls (10.1 pg/mu g), and FRDA patients (5.7 pg/mu g). The treatment was well tolerated by most patients, and only some of them experienced minor adverse effects at the beginning of the trial.ConclusionsCalcitriol dosage used (0.25 mcg/24 h) is safe for FRDA patients, and it increases frataxin levels. We cannot rule out that higher doses administered longer could yield neurological benefits. (c) 2024 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
引用
收藏
页码:1099 / 1108
页数:10
相关论文
共 50 条
  • [21] Effects of Erythropoietin on Frataxin Levels and Mitochondrial Function in Friedreich Ataxia – a Dose–Response Trial
    Wolfgang Nachbauer
    Sascha Hering
    Markus Seifert
    Hannes Steinkellner
    Brigitte Sturm
    Barbara Scheiber-Mojdehkar
    Markus Reindl
    Alexander Strasak
    Werner Poewe
    Guenter Weiss
    Sylvia Boesch
    The Cerebellum, 2011, 10 : 763 - 769
  • [22] Frataxin deficiency increases cyclooxygenase 2 and prostaglandins in cell and animal models of Friedreich's ataxia
    Hayashi, Genki
    Shen, Yan
    Pedersen, Theresa L.
    Newman, John W.
    Pook, Mark
    Cortopassi, Gino
    HUMAN MOLECULAR GENETICS, 2014, 23 (25) : 6838 - 6847
  • [23] Frataxin gene of Friedreich's ataxia is targeted to mitochondria
    Priller, J
    Scherzer, CR
    Faber, PW
    MacDonald, ME
    Young, AB
    ANNALS OF NEUROLOGY, 1997, 42 (02) : 265 - 269
  • [24] Effects of Erythropoietin on Endothelial Progenitor Cells, Frataxin Levels and Oxidative Metabolism in the Skeletal Muscle of Friedreich Ataxia Patients
    Nachbauer, Wolfgang
    Wanschitz, Julia
    Reindl, Markus
    Scheiber-Mojdehkar, Barbara
    Poewe, Werner
    Boesch, Sylvia
    NEUROLOGY, 2010, 74 (09) : A486 - A487
  • [25] Novel Point Mutations in Frataxin Gene in Iranian Patients with Friedreich's Ataxia
    Heidari, Mohammad Mehdi
    Khatami, Mehri
    Pourakrami, Jafar
    IRANIAN JOURNAL OF CHILD NEUROLOGY, 2014, 8 (01) : 32 - 36
  • [26] Dimethyl fumarate dosing in humans increases frataxin expression: A potential therapy for Friedreich's Ataxia
    Jasoliya, Mittal
    Sacca, Francesco
    Sahdeo, Sunil
    Chedin, Frederic
    Pane, Chiara
    Morra, Vincenzo Brescia
    Filla, Alessandro
    Pook, Mark
    Cortopassi, Gino
    PLOS ONE, 2019, 14 (06):
  • [27] Evidence for chromosome fragility at the frataxin locus in Friedreich ataxia
    Kumari, Daman
    Hayward, Bruce
    Nakamura, Asako J.
    Bonner, William M.
    Usdin, Karen
    MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 2015, 781 : 14 - 21
  • [28] Friedreich's ataxia: A frataxin mediated mitochondrial disease?
    Gallagher, CL
    Waclawik, AJ
    Salamat, SM
    Lotz, BP
    Fadic, R
    Harding, CO
    Johns, DR
    Beinlich, BR
    NEUROLOGY, 1998, 50 (04) : A414 - A415
  • [29] Ferroxidase activity of frataxin, the protein deficient in Friedreich ataxia
    Gakh, O
    Park, S
    Mooney, SM
    O'Neill, HA
    Nichol, HK
    Pickering, IJ
    George, GN
    Mangravita, A
    Ferreira, GC
    Isaya, G
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 331 - 331
  • [30] Effects of Erythropoietin on Frataxin Levels and Mitochondrial Function in Friedreich Ataxia - a Dose-Response Trial
    Nachbauer, Wolfgang
    Hering, Sascha
    Seifert, Markus
    Steinkellner, Hannes
    Sturm, Brigitte
    Scheiber-Mojdehkar, Barbara
    Reindl, Markus
    Strasak, Alexander
    Poewe, Werner
    Weiss, Guenter
    Boesch, Sylvia
    CEREBELLUM, 2011, 10 (04): : 763 - 769