Genotype-phenotype correlation in pseudoxanthoma elasticum. (May 2021)

• Record Type: Journal Article
• Authors: Bartstra, Jonas W.; Risseeuw, Sara; de Jong, Pim A.; van Os, Bram; Kalsbeek, Lianne; Mol, Chris; Baas, Annette F.; Verschuere, Shana; Vanakker, Olivier; Florijn, Ralph J.; Hendrikse, Jeroen; Mali, Willem; Imhof, Saskia; Ossewaarde-van Norel, Jeannette; van Leeuwen, Redmer; Spiering, Wilko
• Is Part Of: Atherosclerosis. Volume 324(2021)
• Page Start: 18
• Page End: 26
• Publication Date: 2021-05
• Subjects: Pseudoxanthoma elasticum -- Arterial calcification -- Peripheral arterial disease -- ABCC6 -- Genotype-phenotype -- Choroidal neovascularization; Arteriosclerosis -- Periodicals; Electronic journals; 616.136
• DOI: 10.1016/j.atherosclerosis.2021.03.012
• Languages: English
• ISSNs: 0021-9150

Abstract

Abstract: Background and aims: Pseudoxanthoma elasticum (PXE) is caused by variants in the ABCC6 gene. It results in calcification in the skin, peripheral arteries and the eyes, but has considerable phenotypic variability. We investigated the association between the ABCC6 genotype and calcification and clinical phenotypes in these different organs. Methods: ABCC6 sequencing was performed in 289 PXE patients. Genotypes were grouped as two truncating, mixed, or two non-truncating variants. Arterial calcification mass was quantified on whole body, low dose CT scans; and peripheral arterial disease was measured with the ankle brachial index after treadmill test. The presence of pseudoxanthoma in the skin was systematically scored. Ophthalmological phenotypes were the length of angioid streaks as a measure of Bruchs membrane calcification, the presence of choroidal neovascularizations, severity of macular atrophy and visual acuity. Regression models were built to test the age and sex adjusted genotype-phenotype association. Results: 158 patients (median age 51 years) had two truncating variants, 96 (median age 54 years) a mixed genotype, 18 (median age 47 years) had two non-truncating variants. The mixed genotype was associated with lower peripheral (β: 0.39, 95%CI:-0.62;-0.17) and total (β: 0.28, 95%CI:-0.47;-0.10) arterial calcification mass scores, and lower prevalence of choroidal neovascularizations (OR: 0.41 95%CI:0.20; 0.83) compared to two truncating variants. No association with pseudoxanthomas was found. Conclusions: PXE patients with a mixed genotype have less severe arterial and ophthalmological phenotypes than patients with two truncating variants in the ABCC6 gene. Research into environmental and genetic modifiers might provide further insights into the unexplained phenotypic variability. Graphical abstract: Image 1 Highlights: PXE is caused by pathogenic variants in the ABCC6 gene, but no genotype-phenotype association has been established. Patients with two truncating variants have more severe arterial and retinal calcification compared to patients with a mixed genotype. Research into environmental and genetic modifiers might provide further insights into the unexplained phenotypic variability.