What is New in Diagnosis of Amyloidosis?

Main Article Content

María A. Marco
Marcelina Carretero
Diego Pérez de Arenaza
Eugenia Villanueva
Erika B. Brulc
Gisela Bendelman
Elsa M. Nucifora
María S. Sáez
Patricia B. Sorroche
María A. Aguirre
María L Posadas Martínez
Published: 2024-02-28
Keywords:
amyloidosis, amyloidosis diagnosis, TTR amyloidosis, immunoglobulin light-chain amyloidosis, cardiac amyloidosis,, amyloid neuropathies,, amyloidogenesis

Abstract

Amyloidosis has always represented a diagnostic challenge. In 2020, the Amyloidosis Study Group (ASG) developed the "Clinical Practice Guideline for the Diagnosis of Amyloidosis". New lines of research have subsequently emerged. This narrative review aims to explore the state of the art in the diagnosis of amyloidosis diagnosis.


In patients with amyloidosis, protein typing by mass spectrometry is recommended, a technique hard to perform because it requires laser microdissection for sample preparation. Recent publications propose other methods to obtain the amyloid sample to be analyzed, making it possible to dispense with microdissection.


On the other hand, in patients with confirmed TTR amyloidosis (aTTR), the recommendation to sequence the amyloidogenic gene was intended for suspected cases of hereditary aTTR but has now been extended to all patients regardless of age.

Downloads

Download data is not yet available.

Article Details

Section

Update and advances in research

How to Cite

1.
Marco MA, Carretero M, Pérez de Arenaza D, Villanueva E, Brulc EB, Bendelman G, et al. What is New in Diagnosis of Amyloidosis?. Rev Hosp Ital B.Aires [Internet]. 2024 Feb. 28 [cited 2026 Jul. 26];43(4):209-13. Available from: https://ojs.hospitalitaliano.org.ar/index.php/revistahi/article/view/226

References

Posadas Martinez ML, Aguirre MA, Belziti C, Brouet E, Auteri MA, Forte AL, et al. 74-82. Guía de Práctica Clínica para el diagnóstico de la amiloidosis: Parte 1/3. Año 2020. 2021 03 12. Rev Fac Cien Med Univ Nac Cordoba. 2021 Mar 12;78(1):74–82. Disponible en: https://revistas.unc.edu.ar/index.php/med/article/view/30824/33103 DOI: https://doi.org/10.31053/1853.0605.v78.n1.30824

Posadas Martinez ML, Nucifora E, Belziti C, Auteri MA, Pitzus AE, Dragonetti L, et al. Clinical Practice Guidelines for diagnosis of organic involvement of amyloidosis: Part 2/3.Year 2020. Rev Fac Cien Med Univ Nac Cordoba. 2022 Mar 7;79(1):78–87. Disponible en: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9004298/ DOI: https://doi.org/10.31053/1853.0605.v79.n1.30897

Martinez MLP, Aguirre MA, Greloni G, Marciano S, Perez de Arenaza D, Rugiero M, et al. Guía de Práctica Clínica para el diagnóstico de compromiso orgánico en amiloidosis: Parte 3/3 Año 2020: GPC compromiso orgánico en amiloidosis. Rev Fac Cien Med Univ Nac Cordoba. 2022 Dec 21;79(4):391–9. DOI: https://doi.org/10.31053/1853.0605.v79.n4.30903

Kamiie J, Aihara N, Uchida Y, Kobayashi D, Yoshida Y, Kuroda T, Sakaue M et a. Amyloid-specific extraction using organic solvents. Methods X. 2021 Sept. Disponible en: https://doi.org/10.1016/j.mex.2019.100770 DOI: https://doi.org/10.1016/j.mex.2019.100770

Phipps WS, Smith KD, Yang HY, Henderson CM, Pflaum H, Lerch ML, et al. Tandem Mass Spectrometry-Based Amyloid Typing Using Manual Microdissection and Open-Source Data Processing. Am J Clin Pathol. 2022 May 4;157(5):748–57. DOI: https://doi.org/10.1093/ajcp/aqab185

Garcia-Pavia P, Rapezzi C, Adler Y, Arad M, Basso C, Brucato A, et al. Diagnosis and treatment of cardiac amyloidosis: a position statement of the ESC Working Group on Myocardial and Pericardial Diseases [Internet]. Vol. 42, European Heart Journal. 2021. p. 1554–68. Disponible en: http://dx.doi.org/10.1093/eurheartj/ehab072. DOI: https://doi.org/10.1093/eurheartj/ehab072

Jiang S, Zhang L, Wang J, Li X, Hu S, Fu Y, et al. Differentiating between cardiac amyloidosis and hypertrophic cardiomyopathy on non-contrast cine-magnetic resonance images using machine learning-based radiomics. Front Cardiovasc Med. 2022 Oct 26;9:1001269. Disponible en: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643770/ DOI: https://doi.org/10.3389/fcvm.2022.1001269

Ticau S, Sridharan GV, Tsour S, Cantley WL, Chan A, Gilbert JA, et al. Neurofilament Light Chain as a Biomarker of Hereditary Transthyretin-Mediated Amyloidosis. Neurology. 2021 Jan 19;96(3):e412–22. Disponible en: https://pubmed.ncbi.nlm.nih.gov/33087494/ DOI: https://doi.org/10.1212/WNL.0000000000011090

Louwsma J, Brunger AF, Bijzet J, Kroesen BJ, Roeloffzen WWH, Bischof A, et al. Neurofilament light chain, a biomarker for polyneuropathy in systemic amyloidosis. Amyloid. 2021 Mar;28(1):50–5. Disponible en: https://www.tandfonline.com/doi/full/10.1080/13506129.2020.1815696 DOI: https://doi.org/10.1080/13506129.2020.1815696

Dispenzieri A, Larson DR, Rajkumar SV, Kyle RA, Kumar SK, Kourelis T, et al. N-glycosylation of monoclonal light chains on routine MASS-FIX testing is a risk factor for MGUS progression. Leukemia. 2020 Oct;34(10):2749–53. Disponible en: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7529948/ DOI: https://doi.org/10.1038/s41375-020-0940-8

Most read articles by the same author(s)

1 2 > >>