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  2. Amyloid cardiomyopathy - Wikipedia

    en.wikipedia.org/wiki/Amyloid_cardiomyopathy

    Chemotherapy can treat amyloidosis if it is related to immunoglobulins. [4] Liver transplant can treat amyloidosis if it is related to familial transthyretin. [4]Acoramidis (Attruby) was approved for medical use in the United States in November 2024, to treat adults with cardiomyopathy of wild-type or variant (hereditary) transthyretin-mediated amyloidosis (ATTR-CM) to reduce death and ...

  3. Wild-type transthyretin amyloid - Wikipedia

    en.wikipedia.org/wiki/Wild-Type_Transthyretin...

    Wild-type transthyretin amyloid (WTTA), also known as senile systemic amyloidosis (SSA), [1] is a disease that typically affects the heart and tendons of elderly people. It is caused by the accumulation of a wild-type (that is to say a normal ) protein called transthyretin .

  4. Familial amyloid cardiomyopathy - Wikipedia

    en.wikipedia.org/wiki/Familial_amyloid_cardiomyo...

    Both mutant and wild-type transthyretin comprise the aggregates because the TTR blood protein is a tetramer composed of mutant and wild-type TTR subunits in heterozygotes. Several mutations in TTR are associated with FAC, including V122I, V20I, P24S, A45T, Gly47Val, Glu51Gly, I68L, Gln92Lys, and L111M.

  5. Attruby™ (acoramidis), a Near Complete TTR Stabilizer (≥90% ...

    lite.aol.com/tech/story/0022/20241122/9279002.htm

    "Transthyretin cardiac amyloidosis is a progressive disease with a poor prognosis when left untreated. Having a new first line treatment option which provides excellent TTR stabilization and improves outcomes in this disease gives patients more options,” said Martha Grogan, M.D., of the Mayo Clinic.

  6. Amyloidosis - Wikipedia

    en.wikipedia.org/wiki/Amyloidosis

    Survival diminishes with increasing stage, but recent advancements in treatments have improved median survival rates for stages I, II, and III, to 91.2, 60, and 7 months respectively. [45] Outcomes in a person with AA amyloidosis depend on the underlying disease, organ(s) affected, and correlate with the concentration of serum amyloid A protein ...

  7. AL amyloidosis - Wikipedia

    en.wikipedia.org/wiki/AL_amyloidosis

    Median survival for patients diagnosed with AL amyloidosis was 13 months in the early 1990s, but had improved to about 40 months a decade later with 5 year survival rates also increasing from 15% in the 1980s to 48% in the mid 2010s . [17] [4] Heart involvement is associated with a worse prognosis. [18]

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