Hereditary hemochromatosis: data from a single center Copenhagen cohort

Abstract

OBJECTIVES: We aimed to describe a cohort of hereditary hemochromatosis (HH) patients from a single urban center in Copenhagen.

METHODS: Retrospectively, data from patients with HH from the years 2009-2020 were collected.

RESULTS: A total of 203 patients was recorded. Males constituted 65.0% of the patients. Homozygous HH (HHH)/compound heterozygous HH (CHH) accounted for 69.4%/30.6%. HHH patients had significantly higher ferritin and transferrin saturation (TS) levels at debut than CHH patients. Fifty-five HHH patients (39.0%) had ferritin >1000 ug/L versus 9 (14.5%) in the CHH group (p < .001). Age at debut did not differ between female and male patients. Ferritin (but not TS) levels were significantly higher in male patients. The proportion of patients with ferritin >1000 did not differ between males and females. One-hundred patients (49.3%) had one or more symptoms at the time of diagnosis; arthralgias of the metacarpophalangeal joints and/or ankles (n = 46 (22.7%)), fatigue (n = 67 (33.0%)) and decreased libido (n = 20 (9.9%)). The proportion of patients with symptoms did not differ between HHH and CHH or between male and female patients. Severe organ complications (cardiomyopathy, late onset type 1 diabetes or cirrhosis) were present in 14 patients (6.9%).

CONCLUSIONS: We report a high proportion of compound HH, constituting almost one-third of patients. We found that the proportion of patients with symptoms did not differ between HHH and CHH and recommend that CHH should be treated and examined in the same way as HHH.

Original languageEnglish
JournalScandinavian Journal of Gastroenterology
Volume57
Issue number8
Pages (from-to)972-977
Number of pages6
ISSN0036-5521
DOIs
Publication statusPublished - Aug 2022

Keywords

  • Female
  • Ferritins
  • Hemochromatosis/diagnosis
  • Hemochromatosis Protein
  • Histocompatibility Antigens Class I
  • Humans
  • Male
  • Membrane Proteins
  • Retrospective Studies

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