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Adenosine Receptors Profile in Fibromuscular Dysplasia
Claire Guiol1, Sarah El Harake2, Julien Fromonot1,3
1Centre for Cardiovascular Research and Nutrition, C2VN, INSERM, INRAE, Aix Marseille University, 13000 Marseille, France.
Insights
Fibromuscular dysplasia (FMD) diagnosis may be improved by measuring adenosine blood levels (ABL) and adenosine A2B receptor (A2BR) production. Elevated ABL and A2BR overproduction were observed in FMD patients, suggesting their potential as diagnostic biomarkers.
Area of Science:
- Vascular Biology
- Biochemistry
- Medical Diagnostics
Background:
- Fibromuscular dysplasia (FMD) is a non-inflammatory vascular disease causing hypertension in young individuals.
- Current diagnosis relies on catheter-angiography, often leading to delays.
- Adenosine and its receptors are potential factors in FMD pathophysiology.
Purpose of the Study:
- To investigate the association between adenosine blood levels (ABL) and adenosine receptor production with FMD.
- To explore the potential of ABL and adenosine receptor A2BR as diagnostic biomarkers for FMD.
Main Methods:
- Evaluated adenosine A1, A2A, and A2B receptor production using Western blot in 67 FMD patients and 40 controls.
- Measured adenosine blood levels (ABL) via liquid chromatography-mass spectrometry.
- Assessed A2BR production cutoff for diagnostic sensitivity and specificity.
Main Results:
- Adenosine blood levels (ABL) were significantly higher in FMD patients (+180%) compared to controls.
- Overproduction of adenosine A2B receptors (A2BR) was found in FMD patients (+65%).
- A2BR production with a cutoff of 1.3 arbitrary units demonstrated good diagnostic sensitivity and specificity.
Conclusions:
- Elevated ABL and A2BR overproduction are associated with FMD.
- Measuring A2BR production on monocytes and ABL may aid in FMD diagnosis, particularly in complex cases.
- These biomarkers offer a potential adjunctive diagnostic tool for FMD.
Abstract:
Fibromuscular dysplasia (FMD) is a non-inflammatory vascular disease that is characterized by unexplained systemic hypertension occurring in young people, associated with arterial stenosis, aneurysm rupture, intracranial/renal infarction, and stroke. Although the gold standard for the diagnosis remains catheter-angiography, biological markers would be helpful due to the delay from first symptom to diagnosis. Adenosine is an ATP derivative, that may be implicated in FMD pathophysiology. We hypothesized that changes in adenosine blood level (ABL) and production of adenosine receptors may be associated with FMD. Using peripheral blood mononuclear cells, we evaluated A1, A2A, and A2B receptor production by Western blot, in 67 patients (17 men and 50 women, mean (range) age 55 (29−77) years and 40 controls, 10 men and 30 women, mean (range) age 56 (37−70)). ABL was evaluated by liquid chromatography, mass spectrometry. ABL was significantly higher in patients vs. controls, mean (range): 1.7 (0.7−3) µmol/L vs. controls 0.6 (0.4−0.8) µmol/L (+180%) p < 0.001. While A1R and A2AR production did not differ in patients and controls, we found an over-production of A2BR in patients: 1.70 (0.90−2.40; arbitrary units) vs. controls = 1.03 (0.70−1.40), mean + 65% (p < 0.001). A2BR production with a cut off of 1.3 arbitrary units, gives a good sensitivity and specificity for the diagnosis. Production measurement of A2BR on monocytes and ABL could help in the diagnosis, especially in atypical or with poor symptoms.
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