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EXPLORE: A Prospective, Multinational, Natural History Study of Patients with Acute Hepatic Porphyria with Recurrent Attacks.
Gouya, Laurent; Ventura, Paolo; Balwani, Manisha; Bissell, D Montgomery; Rees, David C; Stölzel, Ulrich; Phillips, John D; Kauppinen, Raili; Langendonk, Janneke G; Desnick, Robert J; Deybach, Jean-Charles; Bonkovsky, Herbert L; Parker, Charles; Naik, Hetanshi; Badminton, Michael; Stein, Penelope E; Minder, Elisabeth; Windyga, Jerzy; Bruha, Radan; Cappellini, Maria Domenica; Sardh, Eliane; Harper, Pauline; Sandberg, Sverre; Aarsand, Aasne K; Andersen, Janice; Alegre, Félix; Ivanova, Aneta; Talbi, Neila; Chan, Amy; Querbes, William; Ko, John; Penz, Craig; Liu, Shangbin; Lin, Tim; Simon, Amy; Anderson, Karl E.
Afiliação
  • Gouya L; Centre de Référence Maladies Rares Porphyries, Colombes, France.
  • Ventura P; University of Paris, Paris, France.
  • Balwani M; Laboratory of Excellence GR-Ex, Paris, France.
  • Bissell DM; Università degli Studi di Modena e Reggio Emilia, Emilia-Romagna, Italy.
  • Rees DC; Icahn School of Medicine at Mount Sinai, New York, NY.
  • Stölzel U; University of California, San Francisco, CA.
  • Phillips JD; King's College Hospital, King's College London, London, UK.
  • Kauppinen R; Klinikum Chemnitz Porphyria Center, Chemnitz, Germany.
  • Langendonk JG; University of Utah, Salt Lake City, UT.
  • Desnick RJ; University Hospital of Helsinki, Helsinki, Finland.
  • Deybach JC; Porphyria Center, Center for Lysosomal and Metabolic Disease, Department of Internal Medicine, Erasmus MC, University Medical Center Rotterdam, the Netherlands.
  • Bonkovsky HL; Icahn School of Medicine at Mount Sinai, New York, NY.
  • Parker C; Centre de Référence Maladies Rares Porphyries, Colombes, France.
  • Naik H; University of Paris, Paris, France.
  • Badminton M; Laboratory of Excellence GR-Ex, Paris, France.
  • Stein PE; Section on Gastroenterology & Hepatology, Wake Forest University/NC Baptist Medical Center, Winston-Salem, NC.
  • Minder E; University of Utah, Salt Lake City, UT.
  • Windyga J; Icahn School of Medicine at Mount Sinai, New York, NY.
  • Bruha R; University Hospital of Wales, Cardiff, UK.
  • Cappellini MD; King's College Hospital, King's College London, London, UK.
  • Sardh E; Stadtspital Triemli, Zentrallabor, Zurich, Switzerland.
  • Harper P; Department of Hemostatic Disorders and Internal Medicine, Institute of Hematology and Transfusion Medicine, Warsaw, Poland.
  • Sandberg S; 4th Internal Clinic, General University Hospital, Charles University, Prague, Czech Republic.
  • Aarsand AK; Fondazione IRCCS, Ca Granda, University of Milan, Milan, Italy.
  • Andersen J; Porphyria Centre Sweden, Centre for Inherited Metabolic Diseases, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
  • Alegre F; Porphyria Centre Sweden, Centre for Inherited Metabolic Diseases, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden.
  • Ivanova A; Norwegian Porphyria Centre, Haukeland University Hospital, Bergen, Norway.
  • Talbi N; Norwegian Porphyria Centre, Haukeland University Hospital, Bergen, Norway.
  • Chan A; Norwegian Porphyria Centre, Haukeland University Hospital, Bergen, Norway.
  • Querbes W; Clinica Universidad de Navarra, Navarra, Spain.
  • Ko J; St. Ivan Rilski U Hospital, Sofia, Bulgaria.
  • Penz C; Centre de Référence Maladies Rares Porphyries, Colombes, France.
  • Liu S; University of Paris, Paris, France.
  • Lin T; Laboratory of Excellence GR-Ex, Paris, France.
  • Simon A; Alnylam Pharmaceuticals, Cambridge, MA.
  • Anderson KE; Alnylam Pharmaceuticals, Cambridge, MA.
Hepatology ; 71(5): 1546-1558, 2020 05.
Article em En | MEDLINE | ID: mdl-31512765
ABSTRACT
BACKGROUND AND

AIMS:

Acute hepatic porphyria comprises a group of rare genetic diseases caused by mutations in genes involved in heme biosynthesis. Patients can experience acute neurovisceral attacks, debilitating chronic symptoms, and long-term complications. There is a lack of multinational, prospective data characterizing the disease and current treatment practices in severely affected patients. APPROACH AND

RESULTS:

EXPLORE is a prospective, multinational, natural history study characterizing disease activity and clinical management in patients with acute hepatic porphyria who experience recurrent attacks. Eligible patients had a confirmed acute hepatic porphyria diagnosis and had experienced ≥3 attacks in the prior 12 months or were receiving prophylactic treatment. A total of 112 patients were enrolled and followed for at least 6 months. In the 12 months before the study, patients reported a median (range) of 6 (0-52) acute attacks, with 52 (46%) patients receiving hemin prophylaxis. Chronic symptoms were reported by 73 (65%) patients, with 52 (46%) patients experiencing these daily. During the study, 98 (88%) patients experienced a total of 483 attacks, 77% of which required treatment at a health care facility and/or hemin administration (median [range] annualized attack rate 2.0 [0.0-37.0]). Elevated levels of hepatic δ-aminolevulinic acid synthase 1 messenger ribonucleic acid levels, δ-aminolevulinic acid, and porphobilinogen compared with the upper limit of normal in healthy individuals were observed at baseline and increased further during attacks. Patients had impaired quality of life and increased health care utilization.

CONCLUSIONS:

Patients experienced attacks often requiring treatment in a health care facility and/or with hemin, as well as chronic symptoms that adversely influenced day-to-day functioning. In this patient group, the high disease burden and diminished quality of life highlight the need for novel therapies.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Porfirias Hepáticas / Sintase do Porfobilinogênio Tipo de estudo: Observational_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Hepatology Ano de publicação: 2020 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Porfirias Hepáticas / Sintase do Porfobilinogênio Tipo de estudo: Observational_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Hepatology Ano de publicação: 2020 Tipo de documento: Article País de afiliação: França