Role of Diphosphonates Bone Scintigraphy in Correlation with Biomarkers for a Personalized Approach to ATTR Cardiac Amyloidosis in North-Eastern Romania.
Teodor Marian IonescuManuela CiocoiuRaoul-Vasile LupușoruIrena GrierosuRadu Andy SascăuWael JalloulRoxana IacobCati Raluca StolniceanuAlexandra ClementAna-Maria StătescuDaniela CrișuAntoniu Octavian PetrișFlorin MituCipriana ȘtefănescuPublished in: Diagnostics (Basel, Switzerland) (2022)
Transthyretin cardiac amyloidosis (ATTR) is a rare cardiac protein deposition disease characterized by progressive thickening of both ventricles, the inter-atrial-ventricular septum and the atrioventricular valves. The gold standard method for diagnosing this rare pathology is endomyocardial biopsy. If this method cannot be used, the alternative is a mixture of clinical and paraclinical tests. Over the course of five years, we examined 58 patients suspected of cardiac amyloidosis based on electrocardiography and ultrasonography criteria, who had been sent for bone scintigraphy in order to determine the presence of ATTR cardiac amyloidosis. However, the final diagnosis was set by correlating the bone scan with genetic testing, free light chain dosage or soft tissue biopsy. Based on the final diagnosis we analyzed the patients' predominant biomarkers in order to determine a possible correlation between them. This analysis is designed to help the general practitioner set a possible cardiac amyloidosis diagnosis.
Keyphrases
- left ventricular
- soft tissue
- end stage renal disease
- ejection fraction
- newly diagnosed
- multiple myeloma
- heart failure
- bone mineral density
- prognostic factors
- computed tomography
- atrial fibrillation
- magnetic resonance imaging
- patient reported outcomes
- coronary artery disease
- postmenopausal women
- catheter ablation
- tertiary care
- bone loss
- transcatheter aortic valve implantation