Hypertrophic Cardiomyopathy (HCM)

Introduction

Hypertrophic Cardiomyopathy (HCM) is a condition in which the heart muscle thickens abnormally. This thickening can make it harder for the heart to pump blood efficiently. HCM is often genetic and can affect people of all ages, sometimes leading to serious complications.

Causes and Risk Factors

  • Genetic Mutations: HCM is primarily an inherited disorder caused by mutations in genes responsible for heart muscle proteins.
  • Family History: If a close relative has HCM, the risk of developing it increases.
  • Other Conditions: Some metabolic and neuromuscular diseases can also contribute to the development of HCM.

Symptoms

HCM can be asymptomatic in some patients, but common symptoms include:

  • Shortness of breath (dyspnea)
  • Chest pain (angina)
  • Dizziness or fainting (syncope)
  • Palpitations (irregular heartbeats)
  • Fatigue

Diagnosis

To diagnose HCM, doctors use:

  • Echocardiogram (Echo): The primary test to measure heart wall thickness.
  • Electrocardiogram (ECG): Helps detect abnormal heart rhythms.
  • Cardiac MRI: Provides detailed heart imaging.
  • Genetic Testing: Recommended if there is a family history of HCM.

Treatment

Although there is no cure for HCM, treatments can help manage symptoms and prevent complications:

Medications:

  • Beta-blockers and calcium channel blockers to reduce heart workload.
  • Anti-arrhythmic drugs to prevent abnormal rhythms.
  • Anticoagulants if there is a risk of blood clots.

Procedures and Surgeries:

  • Septal Myectomy (surgical removal of thickened heart tissue).
  • Alcohol Septal Ablation (using alcohol injection to reduce heart muscle thickness).
  • Implantable Cardioverter Defibrillator (ICD) for those at risk of sudden cardiac arrest.

Lifestyle Recommendations

  • Regular Check-ups: Essential for monitoring disease progression.
  • Physical Activity: Avoid intense competitive sports but maintain moderate exercise.
  • Dietary Changes: A heart-healthy diet low in salt and fats.
  • Genetic Counseling: For family members at risk of HCM.

Conclusion

HCM is a serious but manageable condition. Early diagnosis and proper treatment can significantly improve quality of life. If you suspect HCM in yourself or a family member, consult a cardiologist for evaluation.

Source recommendations

1. 2020 AHA/ACC Guideline for the Diagnosis and Treatment of Patients With Hypertrophic Cardiomyopathy

  1. https://www.ahajournals.org/doi/10.1161/CIR.0000000000000937
  2. https://pubmed.ncbi.nlm.nih.gov/33215931/
  3. https://www.acc.org/Latest-in-Cardiology/ten-points-to-remember/2020/11/18/18/47/2020-AHA-ACC-Guideline-for-HCM-GL-HCM
  4. https://pubmed.ncbi.nlm.nih.gov/33215938/
  5. https://professional.heart.org/en/science-news/2020-aha-acc-guideline-for-the-diagnosis-and-treatment-of-patients-with-hypertrophic-cardiomyopathy

2. 2023 ESC Guidelines on Cardiomyopathies

  1. https://academic.oup.com/eurheartj/article/44/37/3503/7246608
  2. https://www.escardio.org/Guidelines/Clinical-Practice-Guidelines/Cardiomyopathy-Guidelines
  3. https://pubmed.ncbi.nlm.nih.gov/37622657/
  4. https://www.acc.org/Latest-in-Cardiology/ten-points-to-remember/2023/08/30/02/53/2023-esc-guidelines-for-cardiomyopathies-esc-2023
  5. https://pubmed.ncbi.nlm.nih.gov/38289320/

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