Transthyretin Amyloid and New Treatment Options
This site is intended for healthcare professionals

COMMENTARY

Transthyretin Amyloid and New Treatment Options

Martha Grogan, MD; Melissa A. Lyle, MD; Julie L. Rosenthal, MD

Disclosures

December 06, 2021

0

Editorial Collaboration

Medscape &

This transcript has been edited for clarity.

Martha Grogan, MD: Hello, and welcome back to the Mayo Clinic–Medscape Cardiology video series. I'm Martha Grogan. I am the director of the Cardiac Amyloid Clinic at Mayo Clinic in Rochester, Minnesota.

Today I'm really thrilled to have my colleagues with me, Dr Julie Rosenthal, who is the director of the Cardiac Amyloid Program at Mayo Clinic in Arizona, and Dr Melissa Lyle, who is the cardiac amyloid lead for the Multidisciplinary Amyloid Clinic at Mayo Clinic in Florida. Welcome, Julie and Melissa.

We are going to focus on the new transthyretin amyloidosis (ATTR) therapies today, but I am just going to briefly mention that cardiologists should know that amyloid light-chain amyloidosis (AL) treatment is really improving, especially with the use of daratumumab. This is really a game changer, and with all types of amyloidosis we are now seeing improved outcomes.

We are going to briefly talk a little bit about what is transthyretin amyloid and what are the drugs that we have to treat this condition. Transthyretin is a protein that we all make; it is produced in the liver, and it transports thyroid hormone and retinol binding protein throughout the body.

Comments

3090D553-9492-4563-8681-AD288FA52ACE
Comments on Medscape are moderated and should be professional in tone and on topic. You must declare any conflicts of interest related to your comments and responses. Please see our Commenting Guide for further information. We reserve the right to remove posts at our sole discretion.

processing....