Skip to main content
Top
Published in: Orphanet Journal of Rare Diseases 1/2018

Open Access 01-12-2018 | Letter to the Editor

Basal pharmacokinetic parameters of topically applied diacerein in pediatric patients with generalized severe epidermolysis bullosa simplex

Authors: Michael Ablinger, Thomas K. Felder, Monika Wimmer, Roland Zauner, Peter Hofbauer, Thomas Lettner, Martin Wolkersdorfer, Florian B. Lagler, Anja Diem, Johann W. Bauer, Verena Wally

Published in: Orphanet Journal of Rare Diseases | Issue 1/2018

Login to get access

Abstract

Generalized severe epidermolysis bullosa simplex (EBS-gen sev) is caused by mutations within either the KRT5 or KRT14 gene, phenotypically resulting in blistering and wounding of the skin and mucous membranes after minor mechanical friction. In a clinical phase 2/3 trial, diacerein has recently been shown to significantly reduce blister numbers upon topical application. In this study we addressed basic pharmacokinetic parameters of locally applied diacerein in vitro and in vivo.
Ex vivo experiments using a Franz diffusion cell confirmed the uptake and bio-transformation of diacerein to rhein in a porcine skin model. Rhein, the active metabolite of diacerein, was also detected in both urine and serum samples of two EBS-gen sev patients who topically applied a 1% diacerein ointment over a period of 4 weeks. The accumulated systemic levels of rhein in EBS-gen sev patients were lower than reported levels after oral application.
These preliminary findings point towards the uptake and prolonged persistance of diacerein / rhein within the intended target organ - the skin. Further, they imply an acceptable safety profile at the systemic level.

Trial registration

DRKS. DRKS00005412. Registered 6 November 2013.
Literature
1.
go back to reference Mavilio F, Pellegrini G, Ferrari S, Di Nunzio F, Di Iorio E, Recchia A, et al. Correction of junctional epidermolysis bullosa by transplantation of genetically modified epidermal stem cells. Nat Med. 2006;12:1397–402.CrossRef Mavilio F, Pellegrini G, Ferrari S, Di Nunzio F, Di Iorio E, Recchia A, et al. Correction of junctional epidermolysis bullosa by transplantation of genetically modified epidermal stem cells. Nat Med. 2006;12:1397–402.CrossRef
2.
go back to reference Siprashvili Z, Nguyen NT, Gorell ES, Loutit K, Khuu P, Furukawa LK, et al. Safety and wound outcomes following genetically corrected autologous epidermal grafts in patients with recessive dystrophic epidermolysis bullosa. JAMA. 2016;316:1808–17.CrossRef Siprashvili Z, Nguyen NT, Gorell ES, Loutit K, Khuu P, Furukawa LK, et al. Safety and wound outcomes following genetically corrected autologous epidermal grafts in patients with recessive dystrophic epidermolysis bullosa. JAMA. 2016;316:1808–17.CrossRef
3.
go back to reference Hirsch T, Rothoeft T, Teig N, Bauer JW, Pellegrini G, De Rosa L, et al. Regeneration of the entire human epidermis using transgenic stem cells. Nature. 2017;551:327–32.CrossRef Hirsch T, Rothoeft T, Teig N, Bauer JW, Pellegrini G, De Rosa L, et al. Regeneration of the entire human epidermis using transgenic stem cells. Nature. 2017;551:327–32.CrossRef
4.
go back to reference Pfendner EG, Bruckner AL. Epidermolysis Bullosa Simplex. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, LJH B, Stephens K, Amemiya A, editors. . Seattle: GeneReviews®; 1993-2018. Pfendner EG, Bruckner AL. Epidermolysis Bullosa Simplex. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, LJH B, Stephens K, Amemiya A, editors. . Seattle: GeneReviews®; 1993-2018.
5.
go back to reference Wally V, Hovnanian A, Ly J, Buckova H, Brunner V, Lettner T, et al. Diacerein orphan drug development for epidermolysis bullosa simplex: a phase 2/3 randomized, placebo-controlled, double-blind clinical trial. J Am Acad Dermatol. 2018;78:892–901 e897.CrossRef Wally V, Hovnanian A, Ly J, Buckova H, Brunner V, Lettner T, et al. Diacerein orphan drug development for epidermolysis bullosa simplex: a phase 2/3 randomized, placebo-controlled, double-blind clinical trial. J Am Acad Dermatol. 2018;78:892–901 e897.CrossRef
6.
go back to reference Wally V, Kitzmueller S, Lagler F, Moder A, Hitzl W, Wolkersdorfer M, et al. Topical diacerein for epidermolysis bullosa: a randomized controlled pilot study. Orphanet J Rare Dis. 2013;8:69.CrossRef Wally V, Kitzmueller S, Lagler F, Moder A, Hitzl W, Wolkersdorfer M, et al. Topical diacerein for epidermolysis bullosa: a randomized controlled pilot study. Orphanet J Rare Dis. 2013;8:69.CrossRef
7.
go back to reference Chamcheu JC, Siddiqui IA, Syed DN, Adhami VM, Liovic M, Mukhtar H. Keratin gene mutations in disorders of human skin and its appendages. Arch Biochem Biophys. 2011;508:123–37.CrossRef Chamcheu JC, Siddiqui IA, Syed DN, Adhami VM, Liovic M, Mukhtar H. Keratin gene mutations in disorders of human skin and its appendages. Arch Biochem Biophys. 2011;508:123–37.CrossRef
8.
go back to reference Wally V, Lettner T, Peking P, Peckl-Schmid D, Murauer EM, Hainzl S, et al. The pathogenetic role of IL-1beta in severe epidermolysis bullosa simplex. J Invest Dermatol. 2013;133:1901–3.CrossRef Wally V, Lettner T, Peking P, Peckl-Schmid D, Murauer EM, Hainzl S, et al. The pathogenetic role of IL-1beta in severe epidermolysis bullosa simplex. J Invest Dermatol. 2013;133:1901–3.CrossRef
9.
go back to reference Nicolas P, Tod M, Padoin C, Petitjean O. Clinical pharmacokinetics of diacerein. Clin Pharmacokinet. 1998;35:347–59.CrossRef Nicolas P, Tod M, Padoin C, Petitjean O. Clinical pharmacokinetics of diacerein. Clin Pharmacokinet. 1998;35:347–59.CrossRef
10.
go back to reference Bartosova L, Bajgar J. Transdermal drug delivery in vitro using diffusion cells. Curr Med Chem. 2012;19:4671–7.CrossRef Bartosova L, Bajgar J. Transdermal drug delivery in vitro using diffusion cells. Curr Med Chem. 2012;19:4671–7.CrossRef
11.
go back to reference Layek B, Kumar TS, Trivedi RK, Mullangi R, Srinivas NR. Development and validation of a sensitive LC-MS/MS method with electrospray ionization for quantitation of rhein in human plasma: application to a pharmacokinetic study. Biomed Chromatogr. 2008;22:616–24.CrossRef Layek B, Kumar TS, Trivedi RK, Mullangi R, Srinivas NR. Development and validation of a sensitive LC-MS/MS method with electrospray ionization for quantitation of rhein in human plasma: application to a pharmacokinetic study. Biomed Chromatogr. 2008;22:616–24.CrossRef
12.
go back to reference Liemberger B, Pinon Hofbauer J, Wally V, Arzt C, Hainzl S, Kocher T, et al. RNA trans-splicing modulation via antisense molecule interference. Int J Mol Sci. 2018;19:E762.CrossRef Liemberger B, Pinon Hofbauer J, Wally V, Arzt C, Hainzl S, Kocher T, et al. RNA trans-splicing modulation via antisense molecule interference. Int J Mol Sci. 2018;19:E762.CrossRef
13.
14.
go back to reference Aushev M, Koller U, Mussolino C, Cathomen T, Reichelt J. Traceless targeting and isolation of gene-edited immortalized keratinocytes from epidermolysis bullosa simplex patients. Mol Ther Methods Clin Dev. 2017;6:112–23.CrossRef Aushev M, Koller U, Mussolino C, Cathomen T, Reichelt J. Traceless targeting and isolation of gene-edited immortalized keratinocytes from epidermolysis bullosa simplex patients. Mol Ther Methods Clin Dev. 2017;6:112–23.CrossRef
15.
go back to reference Humbert P, Renaud A, Laurent R, Agache P. Tetracyclines for dystrophic epidermolysis bullosa. Lancet. 1989;2:277.CrossRef Humbert P, Renaud A, Laurent R, Agache P. Tetracyclines for dystrophic epidermolysis bullosa. Lancet. 1989;2:277.CrossRef
16.
go back to reference Ozanic Bulic S, Fassihi H, Mellerio JE, McGrath JA, Atherton DJ. Thalidomide in the management of epidermolysis bullosa pruriginosa. Br J Dermatol. 2005;152:1332–4.CrossRef Ozanic Bulic S, Fassihi H, Mellerio JE, McGrath JA, Atherton DJ. Thalidomide in the management of epidermolysis bullosa pruriginosa. Br J Dermatol. 2005;152:1332–4.CrossRef
17.
go back to reference Fine JD, Manes B, Frangoul H. Systemic granulocyte colony-stimulating factor (G-CSF) enhances wound healing in dystrophic epidermolysis bullosa (DEB): results of a pilot trial. J Am Acad Dermatol. 2015;73:56–61.CrossRef Fine JD, Manes B, Frangoul H. Systemic granulocyte colony-stimulating factor (G-CSF) enhances wound healing in dystrophic epidermolysis bullosa (DEB): results of a pilot trial. J Am Acad Dermatol. 2015;73:56–61.CrossRef
18.
go back to reference Chiaverini C, Fontas E, Vabres P, Bessis D, Mazereeuw J, Charlesworth A, et al. Oral erythromycin therapy in epidermolysis bullosa simplex generalized severe. Br J Dermatol. 2015;173:563–4.CrossRef Chiaverini C, Fontas E, Vabres P, Bessis D, Mazereeuw J, Charlesworth A, et al. Oral erythromycin therapy in epidermolysis bullosa simplex generalized severe. Br J Dermatol. 2015;173:563–4.CrossRef
19.
go back to reference Chiaverini C, Passeron T, Lacour JP. Topical timolol for chronic wounds in patients with junctional epidermolysis bullosa. J Am Acad Dermatol. 2016;75:e223–4.CrossRef Chiaverini C, Passeron T, Lacour JP. Topical timolol for chronic wounds in patients with junctional epidermolysis bullosa. J Am Acad Dermatol. 2016;75:e223–4.CrossRef
20.
go back to reference Chiaverini C, Roger C, Fontas E, Bourrat E, Bourdon-Lanoy E, Labreze C, et al. Oral epigallocatechin-3-gallate for treatment of dystrophic epidermolysis bullosa: a multicentre, randomized, crossover, double-blind, placebo-controlled clinical trial. Orphanet J Rare Dis. 2016;11:31.CrossRef Chiaverini C, Roger C, Fontas E, Bourrat E, Bourdon-Lanoy E, Labreze C, et al. Oral epigallocatechin-3-gallate for treatment of dystrophic epidermolysis bullosa: a multicentre, randomized, crossover, double-blind, placebo-controlled clinical trial. Orphanet J Rare Dis. 2016;11:31.CrossRef
21.
go back to reference Bornert O, Peking P, Bremer J, Koller U, van den Akker PC, Aartsma-Rus A, et al. RNA-based therapies for genodermatoses. Exp Dermatol. 2017;26:3–10.CrossRef Bornert O, Peking P, Bremer J, Koller U, van den Akker PC, Aartsma-Rus A, et al. RNA-based therapies for genodermatoses. Exp Dermatol. 2017;26:3–10.CrossRef
22.
go back to reference Nystrom A, Bernasconi R, Bornert O. Therapies for genetic extracellular matrix diseases of the skin. Matrix Biol. 2018;71:330–47.CrossRef Nystrom A, Bernasconi R, Bornert O. Therapies for genetic extracellular matrix diseases of the skin. Matrix Biol. 2018;71:330–47.CrossRef
23.
go back to reference Kerns ML, Guss L, Fahey J, Cohen B, Hakim JM, Sung S, et al. Randomized, split-body, single-blinded clinical trial of topical broccoli sprout extract: assessing the feasibility of its use in keratin-based disorders. J Am Acad Dermatol. 2017;76:449–53.CrossRef Kerns ML, Guss L, Fahey J, Cohen B, Hakim JM, Sung S, et al. Randomized, split-body, single-blinded clinical trial of topical broccoli sprout extract: assessing the feasibility of its use in keratin-based disorders. J Am Acad Dermatol. 2017;76:449–53.CrossRef
24.
go back to reference Weiner M, Stein A, Cash S, de Leoz J, Fine JD. Tetracycline and epidermolysis bullosa simplex: a double-blind, placebo-controlled, crossover randomized clinical trial. Br J Dermatol. 2004;150:613–4.CrossRef Weiner M, Stein A, Cash S, de Leoz J, Fine JD. Tetracycline and epidermolysis bullosa simplex: a double-blind, placebo-controlled, crossover randomized clinical trial. Br J Dermatol. 2004;150:613–4.CrossRef
25.
go back to reference Veien NK, Buus SK. Treatment of epidermolysis bullosa simplex (EBS) with tetracycline. Arch Dermatol. 2000;136:424–5.CrossRef Veien NK, Buus SK. Treatment of epidermolysis bullosa simplex (EBS) with tetracycline. Arch Dermatol. 2000;136:424–5.CrossRef
26.
go back to reference Retief CR, Malkinson FD, Pearson RW. Two familial cases of epidermolysis bullosa simplex successfully treated with tetracycline. Arch Dermatol. 1999;135:997–8.CrossRef Retief CR, Malkinson FD, Pearson RW. Two familial cases of epidermolysis bullosa simplex successfully treated with tetracycline. Arch Dermatol. 1999;135:997–8.CrossRef
27.
go back to reference Abitbol RJ, Zhou LH. Treatment of epidermolysis bullosa simplex, weber-Cockayne type, with botulinum toxin type a. Arch Dermatol. 2009;145:13–5.CrossRef Abitbol RJ, Zhou LH. Treatment of epidermolysis bullosa simplex, weber-Cockayne type, with botulinum toxin type a. Arch Dermatol. 2009;145:13–5.CrossRef
Metadata
Title
Basal pharmacokinetic parameters of topically applied diacerein in pediatric patients with generalized severe epidermolysis bullosa simplex
Authors
Michael Ablinger
Thomas K. Felder
Monika Wimmer
Roland Zauner
Peter Hofbauer
Thomas Lettner
Martin Wolkersdorfer
Florian B. Lagler
Anja Diem
Johann W. Bauer
Verena Wally
Publication date
01-12-2018
Publisher
BioMed Central
Published in
Orphanet Journal of Rare Diseases / Issue 1/2018
Electronic ISSN: 1750-1172
DOI
https://doi.org/10.1186/s13023-018-0940-1

Other articles of this Issue 1/2018

Orphanet Journal of Rare Diseases 1/2018 Go to the issue