You can confirm or exclude ATTRv amyloidosis through genetic testing

16. 3. 2022

Confirm the diagnosis of ATTRv
amyloidosis in your patients
with GeneAct™

Hereditary transthyretin amyloidosis (ATTRv or hATTR) is a progressive and potentially fatal multi-organ disease.¹ Given the considerable diversity of symptoms, including neurological and cardiac ones, diagnosing ATTRv amyloidosis can often be challenging.¹

Genetic testing is a crucial part of diagnostic procedures and recommendations. Testing the gene encoding
transthyretin (TTR) should be performed on patients with warning signs or a family history of ATTRv amyloidosis.^1, 6

Due to the rapid progression of the disease, early and accurate diagnosis
is significantly beneficial for patients with ATTRv amyloidosis.^{2, 3, 5, 7, 8}
Genetic testing helps shorten the time to diagnosis and accelerate the initiation of appropriate treatment.²

A new diagnostic service has been launched

A free service easing the diagnosis of ATTRv amyloidosis is now available to you and your patients through a partnership between Alnylam and ARCHIMEDLife.

GeneAct™ is a trademark of Alnylam Pharmaceuticals

GeneAct™ enables the identification of ATTRv amyloidosis in patients over 18 years old who have a family history of the disease or exhibit neurological, orthopedic, cardiac, or other symptoms associated with ATTRv amyloidosis, such as:⁶

• Sensory neuropathy
• Motor neuropathy
• Autonomic nervous system disorders
• Heart disease
• Bilateral carpal tunnel syndrome
• Lumbar spinal canal stenosis
• Renal abnormalities
• Ocular changes
• Atypical chronic inflammatory
demyelinating polyneuropathy (CIDP)
• Atypical motor neuron disease (MND)
• Gait and posture disturbances
• Unexplained weight loss
• Positive imaging/biopsy findings

The GeneAct™ service is supported by Alnylam, so you and your patients can use it for free.

You are about to visit a website that is not under the control of Alnylam Pharmaceuticals. Therefore, Alnylam does not endorse its content and is not responsible for its accuracy or practices/standards it includes. Alnylam Pharmaceuticals is not responsible for the security level of third-party websites. All contained trademarks are the property of their respective owners.

If you suspect ATTRv
amyloidosis, request testing

If you have any questions, send them by email to info@archimedlife.com

Alnylam provides financial support for GeneAct™ testing, but the responsibility for the services remains with ARCHIMEDLife.

References:
1. Maurer MS, et al. for the Amyloidosis Research Consortium. Circ Heart Fail. 2019; 12(9): e006075.
2. Adams D, et al. Nat Rev Neurol. 2019; 15(7): 387–404.
3. Swiecicki PL, et al. Amyloid. 2015; 22(2): 123–131.
4. Sattianayagam PT, et al. Eur Heart J. 2012; 33(9): 1120–1127.
5. González-Duarte A, et al. J Neurol. 2020; 267(3): 703–712.
6. Adams D, et al. J Neurol. 2021; 268(6): 2109–2122.
7. Polydefkis M, et al. Presented at PNS Annual Meeting; 22–26 June 2019; Genoa, Italy.
8. Kristen AV, et al. Neurodegener Dis Manag. 2019; 9(1): 5–23.

For physicians only
Created and financed by Alnylam Pharmaceuticals

NP-CZE-00034 | July 2021

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Whole article

You can confirm or exclude ATTRv amyloidosis through genetic testing

Confirm the diagnosis of ATTRv amyloidosis in your patients with GeneAct™

A new diagnostic service has been launched

If you suspect ATTRv amyloidosis, request testing

Labels

Confirm the diagnosis of ATTRv
amyloidosis in your patients
with GeneAct™

If you suspect ATTRv
amyloidosis, request testing