Acute hepatic porphyria in Denmark; a retrospective study
Magnus Emil Ulrich Wagner, Morten Frost, Jan Frystyk

TL;DR
This study examines the characteristics of acute hepatic porphyria patients in Denmark, focusing on symptoms, hospitalizations, and disease subtypes over five years.
Contribution
The study provides a detailed retrospective analysis of AHP in Denmark, highlighting gender and subtype distribution and symptom correlations.
Findings
AIP was the most common AHP subtype, with 100 out of 129 patients.
Symptoms were more common in patients with high baseline PBG excretion.
Females were more likely to experience symptoms and dominate the symptomatic group.
Abstract
Acute hepatic porphyria (AHP) constitutes a class of rare diseases caused by reduced function in enzymes of the heme-biosynthetic pathway. AHP includes acute intermittent porphyria (AIP), hereditary coproporphyria (HCP), variegate porphyria (VP) and the extremely rare δ-aminolevulinic-dehydrase deficiency porphyria (ADP). This retrospective study describes characteristics of the Danish AHP patient population. Department of Endocrinology at Odense University Hospital serves as national AHP center. We performed a 5-year retrospective description of our AHP cohort using electronic patient journals. We included general symptoms, number of acute attacks, hospitalization rates, long-term sequelae and symptoms, and grouped patients according to creatinine-adjusted urinary baseline excretion (i.e., outside attacks) of the porphyrin precursor porphobilinogen (PBG) in normal-, moderate- and…
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Taxonomy
TopicsPorphyrin Metabolism and Disorders · Heme Oxygenase-1 and Carbon Monoxide · Methemoglobinemia and Tumor Lysis Syndrome
