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A Plasma Pyrophosphate Cutoff Value for Diagnosing Pseudoxanthoma Elasticum
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Pseudoxanthoma elasticum (PXE) is a rare inherited systemic disease responsible for a juvenile peripheral arterial calcification disease. The clinical diagnosis of PXE is only based on a complex multi-organ phenotypic score and/or genetical analysis. Reduced plasma inorganic pyrophosphate concentration [PPi]p has been linked to PXE. In this study, we used a novel and accurate method to measure [PPi]p in one of the largest cohorts of PXE patients, and we reported the valuable contribution of a cutoff value to PXE diagnosis. Plasma samples and clinical records from two French reference centers for PXE (PXE Consultation Center, Angers, and FAVA-MULTI South Competent Center, Nice) were assessed. Plasma PPi were measured in 153 PXE and 46 non-PXE patients. The PPi concentrations in the plasma samples were determined by a new method combining enzymatic and ion chromatography approaches. The best match between the sensitivity and specificity (Youden index) for diagnosing PXE was determined by ROC analysis. [PPi]p were lower in PXE patients (0.92 ± 0.30 µmol/L) than in non-PXE patients (1.61 ± 0.33 µmol/L, p < 0.0001), corresponding to a mean reduction of 43 ± 19% (SD). The PPi cutoff value for diagnosing PXE in all patients was 1.2 µmol/L, with a sensitivity of 83.3% and a specificity of 91.1% (AUC = 0.93), without sex differences. In patients aged <50 years (i.e., the age period for PXE diagnosis), the cutoff PPi was 1.2 µmol/L (sensitivity, specificity, and AUC of 93%, 96%, and 0.97, respectively). The [PPi]p shows high accuracy for diagnosing PXE; thus, quantifying plasma PPi represents the first blood assay for diagnosing PXE.
Title: A Plasma Pyrophosphate Cutoff Value for Diagnosing Pseudoxanthoma Elasticum
Description:
Pseudoxanthoma elasticum (PXE) is a rare inherited systemic disease responsible for a juvenile peripheral arterial calcification disease.
The clinical diagnosis of PXE is only based on a complex multi-organ phenotypic score and/or genetical analysis.
Reduced plasma inorganic pyrophosphate concentration [PPi]p has been linked to PXE.
In this study, we used a novel and accurate method to measure [PPi]p in one of the largest cohorts of PXE patients, and we reported the valuable contribution of a cutoff value to PXE diagnosis.
Plasma samples and clinical records from two French reference centers for PXE (PXE Consultation Center, Angers, and FAVA-MULTI South Competent Center, Nice) were assessed.
Plasma PPi were measured in 153 PXE and 46 non-PXE patients.
The PPi concentrations in the plasma samples were determined by a new method combining enzymatic and ion chromatography approaches.
The best match between the sensitivity and specificity (Youden index) for diagnosing PXE was determined by ROC analysis.
[PPi]p were lower in PXE patients (0.
92 ± 0.
30 µmol/L) than in non-PXE patients (1.
61 ± 0.
33 µmol/L, p < 0.
0001), corresponding to a mean reduction of 43 ± 19% (SD).
The PPi cutoff value for diagnosing PXE in all patients was 1.
2 µmol/L, with a sensitivity of 83.
3% and a specificity of 91.
1% (AUC = 0.
93), without sex differences.
In patients aged <50 years (i.
e.
, the age period for PXE diagnosis), the cutoff PPi was 1.
2 µmol/L (sensitivity, specificity, and AUC of 93%, 96%, and 0.
97, respectively).
The [PPi]p shows high accuracy for diagnosing PXE; thus, quantifying plasma PPi represents the first blood assay for diagnosing PXE.
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Funding Acknowledgements
Type of funding sources: None.
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