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Erschienen in: Orphanet Journal of Rare Diseases 1/2013

Open Access 01.12.2013 | Research

Perhexiline maleate in the treatment of fibrodysplasia ossificans progressiva: an open-labeled clinical trial

verfasst von: Hiroshi Kitoh, Masataka Achiwa, Hiroshi Kaneko, Kenichi Mishima, Masaki Matsushita, Izumi Kadono, John D Horowitz, Benedetta C Sallustio, Kinji Ohno, Naoki Ishiguro

Erschienen in: Orphanet Journal of Rare Diseases | Ausgabe 1/2013

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Abstract

Background

Currently, there are no effective medical treatment options to prevent the formation of heterotopic bones in fibrodysplasia ossificans progressiva (FOP). By the drug repositioning strategy, we confirmed that perhexiline maleate (Pex) potentially ameliorates heterotopic ossification in model cells and mice. Here, we conducted a prospective study to assess the efficacy and safety of Pex in the treatment of FOP patients.

Methods

FOP patients in this open-label single-center study were treated with Pex for a total of 12 months, and followed up for 12 consecutive months after medication discontinuation. The safety of the treatment was assessed regularly by physical and blood examinations. The efficacy of Pex for preventing heterotopic ossifications was evaluated by the presence of flare-ups, measurements of serum bone markers, and changes in the total bone volume calculated by the three-dimensional computed tomography (3D-CT) images.

Results

Five patients with an average age of 23.4 years were enrolled. Within safe doses of Pex administration in each individual, there were no drug-induced adverse effects during the medication phase. Three patients showed no intense inflammatory reactions during the study period, while two patients had acute flare-ups around the hip joint without evidence of trauma during the medication phase. In addition, one of them became progressively incapable of opening her mouth over the discontinuation phase. Serum levels of alkaline phosphatase (ALP) and bone specific ALP (BAP) were significantly and synchronously increased with the occurrence of flare-ups. Volumetric 3D-CT analysis demonstrated a significant increase in the total bone volume of Case 2 (378 cm3) and Case 3 (833 cm3) during the two-year study period.

Conclusions

We could not prove the efficacy of oral Pex administration in the prevention of heterotopic ossifications in FOP. Serum levels of ALP and BAP appear to be promising biomarkers for monitoring the development of ectopic ossifications and efficacy of the therapy. Quantification of change in the total bone volume by whole body CT scanning could be a reliable evaluation tool for disease progression in forthcoming clinical trials of FOP.
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Literatur
1.
Zurück zum Zitat Shore EM, Feldman GJ, Xu M, Kaplan FS: The genetics of fibrodysplasia ossificans progressiva. Clin Rev Bone Miner Metab. 2005, 3: 201-204. 10.1385/BMM:3:3-4:201.CrossRef Shore EM, Feldman GJ, Xu M, Kaplan FS: The genetics of fibrodysplasia ossificans progressiva. Clin Rev Bone Miner Metab. 2005, 3: 201-204. 10.1385/BMM:3:3-4:201.CrossRef
2.
Zurück zum Zitat Shore EM, Xu M, Feldman GJ, Fenstermacher DA, Cho T-J, Choi IH, Connor JM, Delai P, Glaser DL, Le Merrer M, Morhart R, Rogers JG, Smith R, Triffitt JT, Urtizberea JA, Zasloff M, Brown MA, Kaplan FS: A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva. Nat Genet. 2006, 38: 525-527. 10.1038/ng1783.PubMedCrossRef Shore EM, Xu M, Feldman GJ, Fenstermacher DA, Cho T-J, Choi IH, Connor JM, Delai P, Glaser DL, Le Merrer M, Morhart R, Rogers JG, Smith R, Triffitt JT, Urtizberea JA, Zasloff M, Brown MA, Kaplan FS: A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva. Nat Genet. 2006, 38: 525-527. 10.1038/ng1783.PubMedCrossRef
3.
Zurück zum Zitat Kaplan FS, Chakkalakal SA, Shore EM: Fibrodysplasia ossificans progressiva: mechanisms and models of skeletal metamorphosis. Dis Model Mech. 2012, 5: 756-762. 10.1242/dmm.010280.PubMedCentralPubMedCrossRef Kaplan FS, Chakkalakal SA, Shore EM: Fibrodysplasia ossificans progressiva: mechanisms and models of skeletal metamorphosis. Dis Model Mech. 2012, 5: 756-762. 10.1242/dmm.010280.PubMedCentralPubMedCrossRef
4.
Zurück zum Zitat Pignolo RJ, Shore EM, Kaplan FS: Fibrodysplasia ossificans progressiva: Clinical and genetic aspects. Orphanet J Rare Dis. 2011, 6: 80-10.1186/1750-1172-6-80.PubMedCentralPubMedCrossRef Pignolo RJ, Shore EM, Kaplan FS: Fibrodysplasia ossificans progressiva: Clinical and genetic aspects. Orphanet J Rare Dis. 2011, 6: 80-10.1186/1750-1172-6-80.PubMedCentralPubMedCrossRef
5.
Zurück zum Zitat Cohen RB, Hahn GV, Tabas JA, Peeper J, Levitz CL, Sando A, Sando N, Zasloff M, Kaplan FS: The natural history of heterotopic ossification in patients who have fibrodysplasia ossificans progressiva. A study of forty-four patients. J Bone Joint Surg Am. 1993, 75: 215-219.PubMed Cohen RB, Hahn GV, Tabas JA, Peeper J, Levitz CL, Sando A, Sando N, Zasloff M, Kaplan FS: The natural history of heterotopic ossification in patients who have fibrodysplasia ossificans progressiva. A study of forty-four patients. J Bone Joint Surg Am. 1993, 75: 215-219.PubMed
6.
Zurück zum Zitat Yu PB, Hong CC, Sachidanandan C, Babitt JL, Deng DY, Hoyng SA, Lin HY, Bloch KD, Peterson RT: Dorsomorphin inhibits BMP signals required for embryogenesis and iron metabolism. Nat Chem Biol. 2008, 4: 33-441. 10.1038/nchembio.2007.54.PubMedCentralPubMedCrossRef Yu PB, Hong CC, Sachidanandan C, Babitt JL, Deng DY, Hoyng SA, Lin HY, Bloch KD, Peterson RT: Dorsomorphin inhibits BMP signals required for embryogenesis and iron metabolism. Nat Chem Biol. 2008, 4: 33-441. 10.1038/nchembio.2007.54.PubMedCentralPubMedCrossRef
7.
Zurück zum Zitat Yu PB, Deng DY, Lai CS, Hong CC, Cuny GD, Bouxsein ML, Hong DW, McManus PM, Katagiri T, Sachidanandan C, et al: BMP type I receptor inhibition reduces heterotopic [corrected] ossification. Nat Med. 2008, 14: 1363-1369. 10.1038/nm.1888.PubMedCentralPubMedCrossRef Yu PB, Deng DY, Lai CS, Hong CC, Cuny GD, Bouxsein ML, Hong DW, McManus PM, Katagiri T, Sachidanandan C, et al: BMP type I receptor inhibition reduces heterotopic [corrected] ossification. Nat Med. 2008, 14: 1363-1369. 10.1038/nm.1888.PubMedCentralPubMedCrossRef
8.
Zurück zum Zitat Shimono K, Tung WE, Macolino C, Chi AH, Didizian JH, Mundy C, Chandraratna RA, Mishina Y, Enomoto-Iwamoto M, Pacifici M, Iwamoto M: Potent inhibition of heterotopic ossification by nuclear retinoic acid receptor-gamma agonists. Nat Med. 2011, 17: 454-460. 10.1038/nm.2334.PubMedCentralPubMedCrossRef Shimono K, Tung WE, Macolino C, Chi AH, Didizian JH, Mundy C, Chandraratna RA, Mishina Y, Enomoto-Iwamoto M, Pacifici M, Iwamoto M: Potent inhibition of heterotopic ossification by nuclear retinoic acid receptor-gamma agonists. Nat Med. 2011, 17: 454-460. 10.1038/nm.2334.PubMedCentralPubMedCrossRef
10.
Zurück zum Zitat Yamamoto R, Matsushita M, Kitoh H, Masuda A, Ito M, Katagiri T, Kawai T, Ishiguro N, Ohno K: Clinically applicable antianginal agents suppress osteoblastic transformation of myogenic cells and heterotopic ossifications in mice. J Bone Miner Metab. 2013, 31: 26-33.PubMed Yamamoto R, Matsushita M, Kitoh H, Masuda A, Ito M, Katagiri T, Kawai T, Ishiguro N, Ohno K: Clinically applicable antianginal agents suppress osteoblastic transformation of myogenic cells and heterotopic ossifications in mice. J Bone Miner Metab. 2013, 31: 26-33.PubMed
11.
Zurück zum Zitat Fukuda T, Kohda M, Kanomata K, Nojima J, Nakamura A, Kamizono J, Noguchi Y, Iwakiri K, Kondo T, Kurose J, Endo K, Awakura T, Fukushi J, Nakashima Y, Chiyonobu T, Kawara A, Nishida Y, Wada I, Akita M, Komori T, Nakayama K, Nanba A, Maruki Y, Yoda T, Tomoda H, Yu PB, Shore EM, Kaplan FS, Miyazomo K, Matsuoka M, et al: Constitutively activated ALK2 and increases SMAD1/5 cooperatively induce bone morphogenetic protein signaling in fibrodysplasia ossificans progressiva. J Biol Chem. 2009, 284: 7149-7156.PubMedCentralPubMedCrossRef Fukuda T, Kohda M, Kanomata K, Nojima J, Nakamura A, Kamizono J, Noguchi Y, Iwakiri K, Kondo T, Kurose J, Endo K, Awakura T, Fukushi J, Nakashima Y, Chiyonobu T, Kawara A, Nishida Y, Wada I, Akita M, Komori T, Nakayama K, Nanba A, Maruki Y, Yoda T, Tomoda H, Yu PB, Shore EM, Kaplan FS, Miyazomo K, Matsuoka M, et al: Constitutively activated ALK2 and increases SMAD1/5 cooperatively induce bone morphogenetic protein signaling in fibrodysplasia ossificans progressiva. J Biol Chem. 2009, 284: 7149-7156.PubMedCentralPubMedCrossRef
12.
Zurück zum Zitat Shah RR, Oates NS, Idle JR, Smith RL, Lockhart JD: Impaired oxidation of debrisoquine in patients with perhexiline neuropathy. Br Med J. 1982, 284: 295-299. 10.1136/bmj.284.6312.295.CrossRef Shah RR, Oates NS, Idle JR, Smith RL, Lockhart JD: Impaired oxidation of debrisoquine in patients with perhexiline neuropathy. Br Med J. 1982, 284: 295-299. 10.1136/bmj.284.6312.295.CrossRef
14.
Zurück zum Zitat Zasloff MA, Roche DM, Crofford LJ, Hahn GV, Kaplan FS: Treatment of patients who have fibrodysplasia ossificans progressiva with isotretinoin. Clin Orthop. 1998, 346: 121-129.PubMedCrossRef Zasloff MA, Roche DM, Crofford LJ, Hahn GV, Kaplan FS: Treatment of patients who have fibrodysplasia ossificans progressiva with isotretinoin. Clin Orthop. 1998, 346: 121-129.PubMedCrossRef
15.
Zurück zum Zitat Brantus JF, Meunier PJ: Effects of intravenous etidronate and oral corticosteroids in fibrodysplasia ossificans progressiva. Clin Orthop. 1998, 346: 117-120.PubMedCrossRef Brantus JF, Meunier PJ: Effects of intravenous etidronate and oral corticosteroids in fibrodysplasia ossificans progressiva. Clin Orthop. 1998, 346: 117-120.PubMedCrossRef
16.
Zurück zum Zitat Blumenkrantz N, Asboe-Hansen G: Fibrodysplasia ossificans progressiva. Biochemical changes in blood serum, urine, skin, bone, and ectopic ossification. Scand J Rheumatol. 1978, 7: 85-89. 10.3109/03009747809098841.PubMedCrossRef Blumenkrantz N, Asboe-Hansen G: Fibrodysplasia ossificans progressiva. Biochemical changes in blood serum, urine, skin, bone, and ectopic ossification. Scand J Rheumatol. 1978, 7: 85-89. 10.3109/03009747809098841.PubMedCrossRef
17.
Zurück zum Zitat Kaplan FS, LeMerrer M, Glaser DL, Pignolo RJ, Goldsby RE, Kitterman JA, Groppe J, Shore EM: Fibrodysplasia ossificans progressiva. Best Pract Res Clin Rheumatol. 2008, 22: 191-205.PubMedCentralPubMedCrossRef Kaplan FS, LeMerrer M, Glaser DL, Pignolo RJ, Goldsby RE, Kitterman JA, Groppe J, Shore EM: Fibrodysplasia ossificans progressiva. Best Pract Res Clin Rheumatol. 2008, 22: 191-205.PubMedCentralPubMedCrossRef
18.
Zurück zum Zitat Ptak T, Rhea JT, Novelline RA: Radiation dose is reduced with a single-pass whole-body multi-detector row CT trauma protocol compared with a conventional segmented method: initial experience. Radiology. 2003, 229: 902-905. 10.1148/radiol.2293021651.PubMedCrossRef Ptak T, Rhea JT, Novelline RA: Radiation dose is reduced with a single-pass whole-body multi-detector row CT trauma protocol compared with a conventional segmented method: initial experience. Radiology. 2003, 229: 902-905. 10.1148/radiol.2293021651.PubMedCrossRef
Metadaten
Titel
Perhexiline maleate in the treatment of fibrodysplasia ossificans progressiva: an open-labeled clinical trial
verfasst von
Hiroshi Kitoh
Masataka Achiwa
Hiroshi Kaneko
Kenichi Mishima
Masaki Matsushita
Izumi Kadono
John D Horowitz
Benedetta C Sallustio
Kinji Ohno
Naoki Ishiguro
Publikationsdatum
01.12.2013
Verlag
BioMed Central
Erschienen in
Orphanet Journal of Rare Diseases / Ausgabe 1/2013
Elektronische ISSN: 1750-1172
DOI
https://doi.org/10.1186/1750-1172-8-163

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