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Relationships between Plasma Pyrophosphate, Vascular Calcification and Clinical Severity in Patients Affected by Pseudoxanthoma Elasticum.
Leftheriotis, Georges; Navasiolava, Nastassia; Clotaire, Laetitia; Duranton, Christophe; Le Saux, Olivier; Bendahhou, Saïd; Laurain, Audrey; Rubera, Isabelle; Martin, Ludovic.
Afiliação
  • Leftheriotis G; University Hospital Nice, Vascular Physiology and Medicine Unit, 06000 Nice, France.
  • Navasiolava N; Université Côte d'Azur, LP2M, UMR CNRS 7370, LabEx ICST, 06107 Nice, France.
  • Clotaire L; PXE Reference Center, MAGEC Nord, University Hospital of Angers, 49000 Angers, France.
  • Duranton C; Université Côte d'Azur, LP2M, UMR CNRS 7370, LabEx ICST, 06107 Nice, France.
  • Le Saux O; Université Côte d'Azur, LP2M, UMR CNRS 7370, LabEx ICST, 06107 Nice, France.
  • Bendahhou S; Department of Cell and Molecular Biology, John A. Burns School of Medicine, University of Hawaii at Manoa, Honolulu, HI 96817, USA.
  • Laurain A; Université Côte d'Azur, LP2M, UMR CNRS 7370, LabEx ICST, 06107 Nice, France.
  • Rubera I; Université Côte d'Azur, LP2M, UMR CNRS 7370, LabEx ICST, 06107 Nice, France.
  • Martin L; Université Côte d'Azur, LP2M, UMR CNRS 7370, LabEx ICST, 06107 Nice, France.
J Clin Med ; 11(9)2022 May 05.
Article em En | MEDLINE | ID: mdl-35566717
ABSTRACT
Pseudoxanthoma elasticum (PXE; OMIM 264800) is an autosomal recessive metabolic disorder characterized by progressive calcification in the skin, the Bruch's membrane, and the vasculature. Calcification in PXE results from a low level of circulating pyrophosphate (PPi) caused by ABCC6 deficiency. In this study, we used a cohort of 107 PXE patients to determine the pathophysiological relationship between plasma PPi, coronary calcification (CAC), lower limbs arterial calcification (LLAC), and disease severity. Overall, our data showed a deficit in plasma PPi in PXE patients compared to controls. Remarkably, affected females showed higher PPi levels than males, but a lower LLAC. There was a strong correlation between age and PPi in PXE patients (r = 0.423, p < 0.0001) but not in controls (r = 0.059, p = 0.828). A weak correlation was found between PPi and CAC (r = 0.266, p < 0.02); however, there was no statistically significant connection with LLAC (r = 0.068, p = 0.518) or a severity score (r = 0.077, p = 0.429). Surprisingly, we found no significant correlation between plasma alkaline phosphatase activity and PPi (r = 0.113, p = 0.252) or between a 10-year cardiovascular risk score and all other variables. Multivariate analysis confirmed that LLAC and CAC were strongly dependent on age, but not on PPi. Our data showed that arterial calcification is only weakly linked to circulating PPi levels and that time (i.e., age) appears to be the major determinant of disease severity and calcification in PXE. These data are important to better understand the natural history of this disease but also for the follow-up and management of patients, and the design of future clinical trials. Our results also show that PPi is not a good biomarker for the evaluation of disease severity and progression.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article