Etidronate for Prevention of Ectopic Mineralization in Patients With Pseudoxanthoma Elasticum

Publication date

2018-03-13

Authors

Kranenburg, Guido
de Jong, PimORCID 0000-0003-4840-6854ISNI 0000000395539334
Bartstra, J. W.
Lagerweij, Suzanne J.
Lam, Marnix G.E.H.ORCID 0000-0002-4902-9790
Ossewaarde-Van Norel, J.ISNI 0000000393375495
Risseeuw, Sara
van Leeuwen, Redmer
Imhof, Saskia M.ISNI 0000000391274981
Verhaar, H JISNI 0000000140632844

Editors

Advisors

Supervisors

Document Type

Article

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License

taverne

Abstract

Background: In pseudoxanthoma elasticum (PXE), low pyrophosphate levels may cause ectopic mineralization, leading to skin changes, visual impairment, and peripheral arterial disease. Objectives: The authors hypothesized that etidronate, a pyrophosphate analog, might reduce ectopic mineralization in PXE. Methods: In the Treatment of Ectopic Mineralization in Pseudoxanthoma Elasticum trial, adults with PXE and leg arterial calcifications (n = 74) were randomly assigned to etidronate or placebo (cyclical 20 mg/kg for 2 weeks every 12 weeks). The primary outcome was ectopic mineralization, quantified with 18fluoride positron emission tomography scans as femoral arterial wall target-to-background ratios (TBRfemoral). Secondary outcomes were computed tomography arterial calcification and ophthalmological changes. Safety outcomes were bone density, serum calcium, and phosphate. Results: During 12 months of follow-up, the TBRfemoral increased 6% (interquartile range [IQR]: −12% to 25%) in the etidronate group and 7% (IQR: −9% to 32%) in the placebo group (p = 0.465). Arterial calcification decreased 4% (IQR: −11% to 7%) in the etidronate group and increased 8% (IQR: −1% to 20%) in the placebo group (p = 0.001). Etidronate treatment was associated with significantly fewer subretinal neovascularization events (1 vs. 9, p = 0.007). Bone density decreased 4% ± 12% in the etidronate group and 6% ± 9% in the placebo group (p = 0.374). Hypocalcemia (<2.20 mmol/l) occurred in 3 versus 1 patient (8.1% vs. 2.7%, p = 0.304). Eighteen patients (48.6%) treated with etidronate, compared with 0 patients treated with placebo (p < 0.001), experienced hyperphosphatemia (>1.5 mmol/l) and recovered spontaneously. Conclusions: In patients with PXE, etidronate reduced arterial calcification and subretinal neovascularization events but did not lower femoral 18fluoride sodium positron emission tomography activity compared with placebo, without important safety issues. (Treatment of Ectopic Mineralization in Pseudoxanthoma elasticum; NTR5180)

Keywords

arterial calcification, bisphosphonates, etidronate, PXE, Taverne, Cardiology and Cardiovascular Medicine

Citation

Kranenburg, G, de Jong, P A, Bartstra, J W, Lagerweij, S J, Lam, M G, Ossewaarde-van Norel, J, Risseeuw, S, van Leeuwen, R, Imhof, S M, Verhaar, H J, de Vries, J J, Slart, R H J A, Luurtsema, G, den Harder, A M, Visseren, F L J, Mali, W P & Spiering, W 2018, 'Etidronate for Prevention of Ectopic Mineralization in Patients With Pseudoxanthoma Elasticum', Journal of the American College of Cardiology, vol. 71, no. 10, pp. 1117-1126. https://doi.org/10.1016/j.jacc.2017.12.062