ATTR-CM Diagnosis

Diagnosing ATTR Cardiac Amyloidosis (ATTR-CM)

ATTR cardiac amyloidosis (ATTR-CM) is a progressive and often underdiagnosed cause of heart failure, particularly in older adults and patients with unexplained left ventricular hypertrophy. Early and accurate diagnosis is essential, as disease-modifying therapies are now available and outcomes improve significantly when treatment begins before advanced cardiac damage occurs.

 

However, ATTR-CM frequently goes unrecognized because its symptoms overlap with more common cardiovascular conditions. A structured and systematic diagnostic approach is therefore critical.

ABOUT US

What Is Transthyretin (TTR)?

ATTR-CM develops when misfolded transthyretin (TTR) proteins aggregate and deposit as amyloid fibrils within the myocardium. These deposits stiffen the heart muscle, impair diastolic filling, and eventually lead to heart failure.

 

Unfortunately, ATTR-CM is often misdiagnosed as:

As a result, many patients experience years of symptoms before receiving the correct diagnosis.

When to Suspect ATTR-CM

Clinical suspicion is the cornerstone of diagnosis. ATTR-CM should be considered in patients with heart failure, especially HFpEF, who present with one or more red flags.

What is amyloidosis showing misfolded amyloid protein accumulation

Cardiac Red Flags

Extracardiac Clues

Recognizing these features early allows clinicians to initiate targeted diagnostic testing.

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OUR HISTORY

Why Amyloidosis Africa Was Born

Amyloidosis Africa is a pan-African initiative that brings together cardiologists from across the continent to address the growing but hidden burden of cardiac amyloidosis. Launched by the Kenya Cardiac Society (KCS) and CRK Clinical Research Key, we aim to raise awareness, educate health professionals, and drive continent-wide research collaboration for early diagnosis and improved patient care.

01

The Start

Amyloidosis Africa began as a clinical collaboration between cardiologists in Kenya, driven by the growing concern of underdiagnosed cardiac amyloidosis in African populations.

02

Growing Together

With support from national societies and research networks, we expanded across Africa, uniting doctors, researchers, and policymakers under one mission: equity in rare disease care.

03

Today

We now serve as a central platform for awareness campaigns, training programs, policy advocacy, and research, shining a light on a once-forgotten disease.

Our Commitment

Continental Engagement

We're working daily with clinicians and institutions across Africa to elevate the diagnosis and treatment of cardiac amyloidosis.

Guidance and support for families affected by amyloidosis

Awareness Campaigns

We develop community outreach and clinical red-flag education to raise awareness across all African regions.

Patient-centered care for cardiac amyloidosis

Policy & Research

We advocate for rare disease inclusion in national plans and support African-led amyloidosis research.

Education & Training

We create diagnostic toolkits and CPD resources tailored to African healthcare settings.

Improving recognition of rare cardiovascular diseases in Africa

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We work toward accessible testing, earlier diagnosis, and support systems for patients and their families.

Patient-centered care for cardiac amyloidosis

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Guidance and support for families affected by amyloidosis

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This survey, coordinated by the Kenya Cardiac Society (KCS) in collaboration with CRK Clinical Research Key (NGO) and partners, aims to better understand the current awareness, diagnostic capacity, and management practices of CA among healthcare providers.

Raising Awareness and Promoting Early Diagnosis of ATTR Cardiac Amyloidosis is a free, CPD-Accredited, self-paced, online CME

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Cardiac amyloidosis is no longer a rare disease, it’s a rarely diagnosed one. Through Amyloidosis Africa, we are reshaping how Africa detects and manages this hidden epidemic.

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