A study of susceptibility-weighted imaging in patients with Wilson disease during the treatment of metal chelator

J Neurol. 2020 Jun;267(6):1643-1650. doi: 10.1007/s00415-020-09746-y. Epub 2020 Feb 14.

Abstract

Objective: A randomized-controlled trial comparing study of the changes in brain sensitive-weighted imaging (SWI) of Wilson disease (WD) patients during the treatment with metal chelator was done.

Methods: 100 untreated WD patients (80 cases of cerebral type, 20 cases of hepatic type, age 20.13 ± 9.12 years old) and 20 normal controls were selected. Neurological symptoms were scored using the modified Young scale. Liver function tests and copper indices were collected. All study objects received SWI test of the brain. The values of corrected phase (CP) were calculated on SWI. Cerebral-type WD patients were treated with D-penicillamine (DPA) (group 1) or Dimercaptopropane Sulfonate (DMPS) + Dimercaptosuccinic Acid (DMSA) (group 2). Hepatic-type WD patients were treated with DPA (group 3). All patients received annual neurological symptom score, liver function, copper indices, and SWI examination.

Results: At the first year of treatment, score of the modified Young scale in group 2 was lower than that in group 1 (P = 0.023) and lower than that before treatment (P = 0.040). After 2 years of treatment, the score of the modified Young scale in group 1 was lower than that before treatment (P = 0.012). At the second year after treatment, the urinary copper in group 2 was higher than that in group 1 (P = 0.014). Urinary copper was maintained at 200 µg/day in group 1 and 300 µg/day in group 2 after 3 years of treatment. At the first year of treatment, serum copper in group 1 was lower than that in group 2 (P = 0.032). At the first year of treatment, CP values of the pallidum and substantia nigra in group 2 were higher than those in group 1 (P = 0.026, 0.040). At the second year of treatment, CP value of substantia nigra in group 2 was higher than that in group 1 (P = 0.037). After 3 years of treatment, there was no difference in CP values between WD patients and normal controls.

Conclusions: Therapy with DMPS and DMSA improves neurological symptoms of WD patients more quickly and leads to less aggravation, compared with therapy with DPA. The metal content in the brain of WD patients was at a low level after 3 years of treatment. DMPS and DMSA can remove metal from brain tissue faster than DPA.

Keywords: Copper metabolism; Neurological symptoms; Sensitive-weighted imaging; Wilson disease.

Publication types

  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Adolescent
  • Adult
  • Chelating Agents / pharmacology*
  • Copper / blood
  • Copper / urine
  • Female
  • Globus Pallidus / diagnostic imaging*
  • Hepatolenticular Degeneration / blood
  • Hepatolenticular Degeneration / diagnostic imaging*
  • Hepatolenticular Degeneration / drug therapy*
  • Hepatolenticular Degeneration / urine
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Outcome Assessment, Health Care
  • Penicillamine / pharmacology*
  • Substantia Nigra / diagnostic imaging*
  • Unithiol / pharmacology*
  • Young Adult

Substances

  • Chelating Agents
  • Unithiol
  • Copper
  • Penicillamine