Literature DB >> 33026560

Porphyric Neuropathy: Pathophysiology, Diagnosis, and Updated Management.

Mohamed Kazamel1, Robert J Desnick2, John G Quigley3.   

Abstract

PURPOSE OF REVIEW: To review the peripheral neurological complications of the acute hepatic porphyrias, as well as the latest advances in their pathophysiology and management. RECENT
FINDINGS: The diagnosis of porphyric neuropathy remains challenging as varying neuropathic patterns are encountered depending on disease stage, including a non-length-dependent distribution pattern. The major pathophysiologic mechanism is δ-aminolevulinic acid (ALA)-induced neurotoxicity. The less restrictive blood-nerve barrier in the autonomic ganglia and myenteric plexus may explain the frequency of dysautonomic manifestations. Recently, a prophylactic small interfering RNA (siRNA)-based therapy that reduces hepatic ALA Synthase-1 mRNA was approved for patients with recurrent neuro-visceral attacks. Neurologists should appreciate the varying patterns of porphyric neuropathy. As with most toxin-induced axonopathies, long-term outcomes depend on early diagnosis and treatment. While the short-term clinical and biochemical benefits of siRNA-based therapy are known, its long-term effects on motor recovery, chronic pain, and dysautonomic manifestations are yet to be determined.

Entities:  

Keywords:  ALA; Dysautonomia; Hemin; Neuropathy; Porphyria; Small interfering RNA

Year:  2020        PMID: 33026560     DOI: 10.1007/s11910-020-01078-8

Source DB:  PubMed          Journal:  Curr Neurol Neurosci Rep        ISSN: 1528-4042            Impact factor:   5.081


  87 in total

1.  delta-Aminolevulinate dehydratase (ALAD) porphyria: the first case in North America with two novel ALAD mutations.

Authors:  Reiko Akagi; Noriko Kato; Rikako Inoue; Karl E Anderson; Eileen K Jaffe; Shigeru Sassa
Journal:  Mol Genet Metab       Date:  2005-12-15       Impact factor: 4.797

2.  Porphyria.

Authors:  D Montgomery Bissell; Karl E Anderson; Herbert L Bonkovsky
Journal:  N Engl J Med       Date:  2017-11-23       Impact factor: 91.245

3.  Acute peripheral neuropathy due to hereditary coproporphyria.

Authors:  R J Barohn; J A Sanchez; K E Anderson
Journal:  Muscle Nerve       Date:  1994-07       Impact factor: 3.217

Review 4.  Acute hepatic porphyrias: Recommendations for evaluation and long-term management.

Authors:  Manisha Balwani; Bruce Wang; Karl E Anderson; Joseph R Bloomer; D Montgomery Bissell; Herbert L Bonkovsky; John D Phillips; Robert J Desnick
Journal:  Hepatology       Date:  2017-09-04       Impact factor: 17.425

5.  Nerve function and dysfunction in acute intermittent porphyria.

Authors:  Cindy S-Y Lin; Arun V Krishnan; Ming-Jen Lee; Alessandro S Zagami; Hui-Ling You; Chih-Chao Yang; Hugh Bostock; Matthew C Kiernan
Journal:  Brain       Date:  2008-07-17       Impact factor: 13.501

6.  delta-Aminolevulinic acid dehydrase (porphobilinogen synthase) in two families with inherited enzyme deficiency.

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Journal:  Clin Genet       Date:  1986-09       Impact factor: 4.438

7.  Acute porphyrias in the USA: features of 108 subjects from porphyrias consortium.

Authors:  Herbert L Bonkovsky; Vinaya C Maddukuri; Cemal Yazici; Karl E Anderson; D Montgomery Bissell; Joseph R Bloomer; John D Phillips; Hetanshi Naik; Inga Peter; Gwen Baillargeon; Krista Bossi; Laura Gandolfo; Carrie Light; David Bishop; Robert J Desnick
Journal:  Am J Med       Date:  2014-07-10       Impact factor: 4.965

8.  The third case of Doss porphyria (delta-amino-levulinic acid dehydratase deficiency) in Germany.

Authors:  M O Doss; T Stauch; U Gross; M Renz; R Akagi; M Doss-Frank; H P Seelig; S Sassa
Journal:  J Inherit Metab Dis       Date:  2004       Impact factor: 4.982

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Authors:  D Montgomery Bissell; Bruce Wang
Journal:  J Clin Transl Hepatol       Date:  2015-03-15

Review 10.  The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine.

Authors:  Peter D Stenson; Matthew Mort; Edward V Ball; Katy Shaw; Andrew Phillips; David N Cooper
Journal:  Hum Genet       Date:  2014-01       Impact factor: 4.132

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  3 in total

1.  Hereditary Coproporphyria Mimicking Guillain-Barré Syndrome After COVID-19 Infection.

Authors:  Margaret Upchurch; Jonathan P Donnelly; Emily Deremiah; Colleen Barthol; Shaheryar Hafeez; Karl E Anderson; Ali Seifi
Journal:  Cureus       Date:  2022-01-25

Review 2.  Inherited Neuromuscular Disorders: Which Role for Serum Biomarkers?

Authors:  Antonino Lupica; Vincenzo Di Stefano; Andrea Gagliardo; Salvatore Iacono; Antonia Pignolo; Salvatore Ferlisi; Angelo Torrente; Sonia Pagano; Massimo Gangitano; Filippo Brighina
Journal:  Brain Sci       Date:  2021-03-21

Review 3.  Mechanisms of Neuronal Damage in Acute Hepatic Porphyrias.

Authors:  Andrea Ricci; Elena Di Pierro; Matteo Marcacci; Paolo Ventura
Journal:  Diagnostics (Basel)       Date:  2021-11-26
  3 in total

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