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Prevalence of ATTR Cardiac Amyloidosis in Patients Undergoing TAVR

The Prevalence of ATTR Cardiac Amyloidosis in Elderly Middle Eastern Patients Undergoing Transarterial Aortic Valve Replacement

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06015997
Enrollment
100
Registered
2023-08-29
Start date
2023-10-01
Completion date
2025-11-01
Last updated
2023-08-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aortic Valve Stenosis, ATTR Amyloidosis Wild Type, Middle East Studies, Severe Aortic Stenosis

Keywords

ATTR cardiac amyloidosis, Severe aortic stenosis, Transarterial aortic valve replacement

Brief summary

ATTR-cardiac amyloidosis (CA) is present in 4% to 16% of elderly patients with severe calcific aortic stenosis (AS). The reasons for this association are not fully known. It is hypothesized that an amyloidotic infiltration of the aortic valve acts as a trigger for the development of endothelial damage and subsequent calcification. Elderly patients undergoing TAVI will be evaluated for the presence of ATTR-CA in Jordan.

Detailed description

ATTR-cardiac amyloidosis (CA) is present in 4% to 16% of elderly patients with severe calcific aortic stenosis (AS). The reasons for this association are not fully known. Two hypotheses may explain this association 1. Amyloidotic infiltration of the aortic valve acts as a trigger for the development of endothelial damage and subsequent calcification. 2. The increased myocardial strain induced by AS may locally favor the process of amyloidogenesis and tissue infiltration. Transarterial AV replacement (TAVI) is the treatment of choice for elderly patients with severe calcific AS. Studies have shown a prevalence of about 10% of ATTR cardiac amyloidosis in patients undergoing TAVI. The diagnosis is based on a positive nuclear scan (PYP, DPD or HMDP) and ruling out AL amyloidosis in patients with positive scans. While studies have shown no impact of ATTR on prognosis in TAVI patients, there is evidence of poorer quality of life, increased in-hospital acute ischemic stroke, increased cardiac and heart failure hospitalizations, increased conduction abnormalities, compared to patients without ATTR undergoing TAVI. The prevalence of ATTR in TAVI patients in Jordan and Middle Eastern populations has not been previously evaluated. The purpose of this study is to evaluate the prevalence of ATTR cardiac amyloidosis in elderly Middle Eastern patients undergoing TAVI and to document the clinical characteristics, procedural outcomes and 1 year follow up of such patients compared to patients without ATTR.

Interventions

None listed

Sponsors

Jordan Collaborating Cardiology Group
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥65 years * Severe aortic stenosis * Patient underwent TAVR procedure * Positive pyruvate PO4 scan

Exclusion criteria

* Diagnosis of AL amyloidosis base on free light chain assay, serum and urine immune electrophoresis.

Design outcomes

Primary

MeasureTime frameDescription
Prevalence of ATTR CA in TAVR patientsOn admission ( from time of admission to time of discharge from the hospital) and within 10 days.Consecutive elderly (≥65 years) patients who are undergoing TAVI will be included. Patients will be invited to undergo a pyruvate PO4 (PYP) scan. Patients with positive scans will undergo further testing to rule out AL amyloidosis (Free light chain assay, SIFEP, UIFEP). Data collection will include all pertinent clinical characteristics, peri- procedural details.
Cardiovascular event at One year follow upOne year after enrollment: up to 30 days after the passage of 365 days after the TAVR procedureEvents at one year defined as the occurrence of all-cause death, and hospital admission for heart failure or aortic valve reintervention.

Contacts

Primary ContactRamzi Tabbalat, MD, FACC
ramzi_md@yahoo.com00962795535522

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026