TRANSTHYRETIN AMYLOIDOSIS. FUNDAMENTALS OF PATHOGENESIS, DIAGNOSIS, TREATMENT, PROGNOSIS



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Abstract

Among the 42 human amyloidoses described to date the so-called systemic tranthyretin amyloidosis (ATTR amyloidosis), which comprises hereditary forms (more than 140 variants in accordance with the number of identified mutations in the transthyretin gene) and a sporadic form without structural changes in the gene and the protein, is of particular interest. This review summarizes modern understandings of pathogenesis of ATTR amyloidosis. The symptoms of different forms of ATTR amyloidosis, issues of early diagnosis, differential diagnosis (including within the group of amyloidoses), advanced therapy and prognosis are considered. Special attention is given to the non-mutant form of ATTR amyloidosis (ATTRwt amyloidosis), the so-called senile amyloidosis, which significantly complicates the course of underlying pathologies in the age group older than 70 years and is still poorly diagnosed. A quite high occurrence of ATTRwt amyloidosis makes it to be considered as a socially significant disease.

About the authors

Mikhail M. Shavlovsky

Institute of Experimental Medicine; Pavlov First Saint Petersburg State Medical University

Email: mmsch@rambler.ru
ORCID iD: 0000-0002-2119-476X
SPIN-code: 5009-9383
ResearcherId: E-4115-2014

MD, PhD, Professor, Head of the Laboratory of Human Molecular Genetics of the Department of Molecular Genetics; Leading Researcher of the Laboratory of Cardiomyopathies of Heart and Vascular Research Institute

Russian Federation, Acad. Pavlov Street 12, Saint-Petersburg, 197022; L'va Tolstogo str. 6-8, Saint Petersburg, 197022

A. Ya. Gudkova

Pavlov First Saint Petersburg State Medical University; Almazov National Medical Research Centre

Email: alexagood-1954@mail.ru
ORCID iD: 0000-0003-0156-8821

MD, PhD, Professor of the Department of Faculty Therapy, Head of the Laboratory of Cardiomyopathies of Heart and Vascular Research Institute; Leading Researcher of the Institute of Molecular Biology and Genetics

Russian Federation, L'va Tolstogo str. 6-8, Saint Petersburg, 197022; Akkuratova street 2, St. Petersburg, 197341

Olga I. Antimonova

Institute of Experimental Medicine

Author for correspondence.
Email: oa0584@mail.ru
ORCID iD: 0000-0003-2843-7688
SPIN-code: 9214-2677
Scopus Author ID: 36019791600

Junior Researcher of the Department of Molecular Genetics

Russian Federation, Acad. Pavlov Street 12, Saint-Petersburg, 197022

A. N Krutikov

Pavlov First Saint Petersburg State Medical University; Almazov National Medical Research Centre

Email: ankrutikov@yandex.ru
ORCID iD: 0000-0001-6897-6171
SPIN-code: 5919-8810

PhD, Senior Researcher of the Laboratory of Cardiomyopathies of Heart and Vascular Research Institute; Leading Researcher of the Scientific Department of Infiltrative Heart Disease

Russian Federation, L'va Tolstogo str. 6-8, Saint Petersburg, 197022; Akkuratova street 2, St. Petersburg, 197341

References

  1. Virchow R. Uber den gang der amyloiden degeneration. Arch Pathol Anat Physiol Klin Med. 1855;8:364–368. (In German). doi: 10.1007/BF01935311
  2. Virchow R. Uber eine im gehirn und ruckenmark des menschen aufgefundene substanz mit der chemischen reaction der cellulose. Arch Pathol Anat Physiol Klin Med. 1854;6:135–138. (In German). doi: 10.1007/BF01930815
  3. Benson MD, Buxbaum JN, Eisenberg DS, et al. Amyloid nomenclature 2018: recommendations by the International Society of Amyloidosis (ISA) nomenclature committee. Amyloid. 2018;25(4):215–219. doi: 10.1080/13506129.2018.1549825
  4. Benson MD, Buxbaum JN, Eisenberg DS, et al. Amyloid nomenclature 2020: update and recommendations by the International Society of Amyloidosis (ISA) nomenclature committee. Amyloid. 2020;27(4):217–222. doi: 10.1080/13506129.2020.1835263
  5. Buxbaum JN, Dispenzieri A, Eisenberg DS, et al. Amyloid nomenclature 2022: update, novel proteins, and recommendations by the International Society of Amyloidosis (ISA) Nomenclature Committee. Amyloid. 2022;29(4):213–219. doi: 10.1080/13506129.2022.2147636
  6. Sipe JD, Cohen AS. Review: history of the amyloid fibril. J Struct Biol. 2000;130(2-3):88–98. doi: 10.1006/jsbi.2000.4221
  7. Gudkova AY, Antimonova OI, Shavlovsky MM. Role of pancreatic amyloidosis in pathogenesis of type 2 diabetes mellitus. Medical academic journal. 2019;19(2):27–36. (In Russ). doi: 10.17816/MAJ19227-36
  8. Iadanza MG, Jackson MP, Hewitt EW, et al. A new era for understanding amyloid structures and disease. Nat Rev Mol Cell Biol. 2018;19(12):755–773. doi: 10.1038/s41580-018-0060-8
  9. Chiti F, Dobson CM. Protein misfolding, amyloid formation, and human disease: A summary of progress over the last decade. Annu Rev Biochem. 2017;86:27–68. doi: 10.1146/annurev-biochem-061516-045115
  10. Shavlovsky MM. Ethiology and pathogenesis of amyloidoses: the molecular and genetic bases. Medical academic journal. 2010;10(4):63–81. (In Russ).
  11. Andrade C. A peculiar form of peripheral neuropathy: familiar atypical generalized amyloidosis with special involvement of the peripheral nerves. Brain. 1952;75(3):408–427. doi: 10.1093/brain/75.3.408
  12. Vieira M, Saraiva MJ. Transthyretin: a multifaceted protein. BioMol Concepts. 2014;5(1):45–54. doi: 10.1515/bmc-2013-0038
  13. Park GY, Jamerlan A, Shim KH, An SAA. Diagnostic and treatment approaches involving transthyretin in amyloidogenic diseases. Int J Mol Sci. 2019;20(12):2982. doi: 10.3390/ijms20122982
  14. Maurer MS, Bokhari S, Damy T, et al. Expert consensus recommendations for the suspicion and diagnosis of transthyretin cardiac amyloidosis. Circ Heart Fail. 2019;12(9):e006075. doi: 10.1161/CIRCHEARTFAILURE.119.006075
  15. Kaku M, Berk JL. Neuropathy associated with systemic amyloidosis. Semin Neurol. 2019;39(5):578–588. doi: 10.1055/s-0039-1688994
  16. Cuddy SAM, Falk RH. Amyloidosis as a systemic disease in context. Can J Cardiol. 2020;36(3):396–407. doi: 10.1016/j.cjca.2019.12.033
  17. Suhr OB, Lundgren E, Westermark P. One mutation, two distinct disease variants: unravelling the impact of transthyretin amyloid fibril composition. J Intern Med. 2017;281(4):337–347. doi: 10.1111/joim.12585
  18. Narotsky DL, Castano A, Weinsaft JW, et al. Wild-type transthyretin cardiac amyloidosis: novel insights from advanced imaging. Can J Cardiol. 2016;32(9):1166.el–1166.e10. doi: 10.1016/j.cjca.2016.05.008
  19. Lemos C, Coelho T, Alves-Ferreira M, et al. Overcoming artefact: anticipation in 284 Portuguese kindreds with familial amyloid polyneuropathy (FAP) ATTRV30M. J Neurol Neurosurg Psychiatry. 2014;85(3):326–330. doi: 10.1136/jnnp-2013-305383
  20. Solovyov KV, Grudinina NA, Semernin EN, et al. Transthyretin gene V30M, H90N, and (del9) mutations in cardiomyopathy patients from St. Petersburg. Russ J Genet. 2011;47(4):477–482. doi: 10.1134/S1022795411020165
  21. Gudkova AYa, Semernin EN, Polyakova AA, et al. The spectrum of mutations of the transthyretin gene in a cohort of patients with chronic heart failure. Translational Medicine. 2016;3(1):34–38. (In Russ). doi: 10.18705/2311-4495-2016-3-1-34-38
  22. Gudkova A.Y., Amelin A.V., Krutikov A.N., et al. Val30Met-transthyrethin amyloid polyneuropathy and cardiomyopathy (review of literature and case report). Consilium Medicum. 2017;19(12):109–116. (In Russ). doi: 10.26442/2075-1753_19.12.109-116
  23. Guselnikova VV, Fedorova EA, Gudkova AJ, et al. Transthyretin amyloid cardiomyopathy. Features of histological diagnosis: study design. Terapevticheskii arkhiv. 2022;94(4):473–478. (In Russ). doi: 10.26442/00403660.2022.04.201464
  24. Gudkova AY, Lapekin SV, Bezhanishvili TG, et al. AL-amyloidosis with cardiac involvement. Diagnostic capabilities of non-invasive methods. Terapevticheskii arkhiv. 2021;93(4):487–496. (In Russ). doi: 10.26442/00403660.2021.04.200689
  25. Gudkova AYa, Polyakova AA, Amelin АV, et al. Non-Val30Met-transthyretin amyloid cardiomyopathy. Literature review and clinical case. Russ J Cardiol. 2018;2(154):121–128. (In Russ). doi: 10.15829/1560-4071-2018-2-121-128
  26. Dispenzieri A, Coelho T, Conceição I, et al. Clinical and genetic profile of patients enrolled in the Transthyretin Amyloidosis Outcomes Survey (THAOS): 14-year update. Orphanet J Rare Dis. 2022;17(1):236. doi: 10.1186/s13023-022-02359-w
  27. Dorbala S, Ando Y, Bokhari S, et al. ASNC/AHA/ASE/EANM/HFSA/ISA/SCMR/SNMMI expert consensus recommendations for multimodality imaging in cardiac amyloidosis: Part 1 of 2-evidence base and standardized methods of imaging. J Nucl Cardiol. 2019;26(6):2065–2123. doi: 10.1007/s12350-019-01760-6
  28. Barroso FA, Coelho T, Dispenzieri A, et al. Characteristics of patients with autonomic dysfunction in the Transthyretin Amyloidosis Outcomes Survey (THAOS). Amyloid. 2022;29(3):175–183. doi: 10.1080/13506129.2022.2043270
  29. González-Duarte A, Barroso F, Mundayat R, Shapiro B. Blood pressure and orthostatic hypotension as measures of autonomic dysfunction in patients from the transthyretin amyloidosis outcomes survey (THAOS). Auton Neurosci. 2019;222:102590. doi: 10.1016/j.autneu.2019.102590
  30. Damy T, Kristen AV, Suhr OB, et al. Transthyretin cardiac amyloidosis in continental Western Europe: an insight through the Transthyretin Amyloidosis Outcomes Survey (THAOS). Eur Heart J. 2022;43(5):391–400. doi: 10.1093/eurheartj/ehz173
  31. Campbell CM, LoRusso S, Dispenzieri A, et al. Sex differences in wild-type transthyretin amyloidosis: an analysis from the Transthyretin Amyloidosis Outcomes Survey (THAOS). Cardiol Ther. 2022;11(3):393–405. doi: 10.1007/s40119-022-00265-7
  32. Smith TJ, Kyle RA, Lie JT. Clinical significance of histopathologic patterns of cardiac amyloidosis. Mayo Clin Proc. 1984;59(8):547–555. doi: 10.1016/s0025-6196(12)61493-1
  33. Koike H, Katsuno M. The ultrastructure of tissue damage by amyloid fibrils. Molecules. 2021;26(15):4611. doi: 10.3390/molecules26154611
  34. Damy T, Jaccard A, Guellich A, et al. Identification of prognostic markers in transthyretin and AL cardiac amyloidosis. Amyloid. 2016;23(3):194–202. doi: 10.1080/13506129.2016.1221815
  35. Binder C, Duca F, Binder T, et al. Prognostic implications of pericardial and pleural effusion in patients with cardiac amyloidosis. Clin Res Cardiol. 2021;110(4):532–543. doi: 10.1007/s00392-020-01698-7
  36. Yamashita T, Ueda M, Misumi Y, et al. Genetic and clinical characteristics of hereditary transthyretin amyloidosis in endemic and non-endemic areas: experience from a single-referral center in Japan. J Neurol. 2018;265(1):134–140. doi: 10.1007/s00415-017-8640
  37. Rubin J, Alvarez J, Teruya S, et al. Hip and knee arthroplasty are common among patients with transthyretin cardiac amyloidosis, occurring years before cardiac amyloid diagnosis: can we identify affected patients earlier? Amyloid. 2017;24(4):226–230. doi: 10.1080/13506129.2017.1375908
  38. Ikeda S-I, Hanyu N, Hongo M, et al. Hereditary generalized amyloidosis with polyneuropathy: clinicopathological study of 65 Japanese patients. Brain. 1987;110(2):315–337. doi: 10.1093/brain/110.2.315
  39. Ferraro PM, D'Ambrosio V, Di Paolantonio A, et al. Renal involvement in hereditary transthyretin amyloidosis: an italian single-centre experience. Brain Sci. 2021;11(8):980. doi: 10.3390/brainsci11080980
  40. Maurer MS, Hanna M, Grogan M, et al. Genotype and phenotype of transthyretin cardiac amyloidosis: THAOS (Transthyretin Amyloid Outcome Survey). J Am Coll Cardiol. 2016;68(2):161–172. doi: 10.1016/j.jacc.2016.03.596
  41. Fenoglio R, Baldovino S, Barreca A, et al. Renal involvement in transthyretin amyloidosis: the double presentation of transthyretin amyloidosis deposition disease. Nephron. 2022;146(5):481–488. doi: 10.1159/000522370
  42. Lobato L. Portuguese-type amyloidosis (transthyretin amyloidosis, ATTR V30M). J Nephrol. 2003;16(3):438–442. PMID: 12832749
  43. Phull P, Sanchorawala V, Connors LH, et al. Monoclonal gammopathy of undetermined significance in systemic transthyretin amyloidosis (ATTR). Amyloid. 2018;25(1):62–67. doi: 10.1080/13506129.2018.1436048
  44. Levin A, Stevens PE, Bilous RW, et al. Kidney disease: improving global outcomes (KDIGO) CKD Work Group. KDIGO 2012 clinical practice guideline for the evaluation and management of chronic kidney disease. Kidney Int Suppl. 2013;3(1):1–150. doi: 10.1038/kisup.2012.73
  45. Solignac J, Delmont E, Fortanier E, et al. Kidney involvement in hereditary transthyretin amyloidosis: a cohort study of 103 patients. Clin Kidney J. 2022;15(9):1747–1754. doi: 10.1093/ckj/sfac118
  46. D'Ambrosio V, Ferraro PM, Guglielmino V, Luigetti M. Kidney involvement in hereditary transthyretin amyloidosis: is there a role for cystatin C? Clin Kidney J. 2022;16(2):397–398. doi: 10.1093/ckj/sfac156
  47. Adams D, Ando Y, Beirão JM, et al. Expert consensus recommendations to improve diagnosis of ATTR amyloidosis with polyneuropathy. J Neurol. 2021;268(6):2109–2122. doi: 10.1007/s00415-019-09688-0
  48. Wixner J, Mundayat R, Karayal ON, et al. THAOS: gastrointestinal manifestations of transthyretin amyloidosis – common complications of a rare disease. Orphanet J Rare Dis. 2014;9:61. doi: 10.1186/1750-1172-9-61
  49. Tereshchenko SN, Zhirov IV, Moiseeva OM, et al. Practical guidelines for the diagnosis and treatment of transthyretin amyloid cardiomyopathy (ATTR-CM or transthyretin cardiac amyloidosis). Terapevticheskii arkhiv. 2022;94(4):584–595. (In Russ). doi: 10.26442/00403660.2022.04.201465
  50. Writing Committee; Kittleson MM, Ruberg FL, Ambardekar AV, et al. 2023 ACC expert consensus decision pathway on comprehensive multidisciplinary care for the patient with cardiac amyloidosis: A report of the American College of Cardiology Solution Set Oversight Committee. J Am Coll Cardiol. 2023;81(11):1076–1126. doi: 10.1016/j.jacc.2022.11.022
  51. Arbelo E, Protonotarios A, Gimeno JR, et al. 2023 ESC guidelines for the management of cardiomyopathies. Eur Heart J. 2023;44(37):3503–3626. doi: 10.1093/eurheartj/ehad194
  52. Moody WE, Turvey-Haigh L, Knight D, et al. British Society of Echocardiography guideline for the transthoracic echocardiographic assessment of cardiac amyloidosis. Echo Res Pract. 2023;10:13. doi: 10.1186/s44156-023-00028-7
  53. Damy T, Maurer MS, Rapezzi C, et al. Clinical, ECG and echocardiographic clues to the diagnosis of TTR-related cardiomyopathy. Open Heart. 2016;3(1):e000289. doi: 10.1136/openhrt-2015-000289
  54. Fabbri G, Serenelli M, Cantone A, et al. Transthyretin amyloidosis in aortic stenosis: clinical and therapeutic implications. Eur Heart J Suppl. 2021;23 Suppl E:E128–132. doi: 10.1093/eurheartj/suab107
  55. Longhi S, Lorenzini M, Gagliardi C, et al. Coexistence of degenerative aortic stenosis and wild-type transthyretin-related cardiac amyloidosis. JACC Cardiovasc Imaging. 2016;9(3):325–327. doi: 10.1016/j.jcmg.2015.04.012
  56. Rapezzi C, Giannini F, Campo G. Aortic stenosis, transcatheter aortic valve replacement and transthyretin cardiac amyloidosis: are we progressively unraveling the tangle? Eur J Heart Fail. 2021;23(2):259–263. doi: 10.1002/ejhf.2057
  57. Caponetti AG, Accietto A, Saturi G, et al. Screening approaches to cardiac amyloidosis in different clinical settings: Current practice and future perspectives. Front Cardiovasc Med. 2023;10:1146725. doi: 10.3389/fcvm.2023.1146725
  58. Bennhold H. Eine spezifische amyloidfarbung mit Kongorot. Munch Med Woch. 1922;69:1537–1538. (In German).
  59. Gusel'nikova VV, Kirik OV, Fyodorova YeA, et al. Rapid method of the amyloid staining with Congo red for light and fluorescence microscopy. Morphologiya. 2016;149(2):84–88. (In Russ).
  60. Antimonova OI, Grudinina NA, Egorov VV et al. Time machine: Can a dye from 1928 be re-purposed for modern, fluorescence-based detection of amyloid-like fibrils? Dyes and Pigments. 2020;172:107863 doi: 10.1016/j.dyepig.2019.107863
  61. Loo D, Mollee PN, Renaut P, Hill MM. Proteomics in molecular diagnosis: typing of amyloidosis. J Biomed Biotechnol. 2011;2011:754109. doi: 10.1155/2011/754109
  62. Sun W, Sun J, Zou L, et al. The successful diagnosis and typing of systemic amyloidosis using a microwave-assisted filter-aided fast sample preparation method and LC/MS/MS analysis. PLoS One. 2015;10(5):e0127180. doi: 10.1371/journal.pone.0127180
  63. Wiseman RL, Green NS, Kelly JW. Kinetic stabilization of an oligomeric protein under physiological conditions demonstrated by a lack of subunit exchange: implication for transthyretin amyloidosis. Biochemistry. 2005;44(25):9265–9274. doi: 10.1021/bi050352o
  64. Coelho T, Merlini G, Bulawa CE et al. Mechanism of action and clinical application of tafamidis in hereditary transthyretin amyloidosis. Neurol Ther. 2016;5(1):1–25. doi: 10.1007/s40120-016-0040-x
  65. Richards DB, Cookson LM, Berges AC, et al. Therapeutic clearance of amyloid by antibodies to serum amyloid P component. N Engl J Med. 2015;373(12):1106–1114. doi: 10.1056/NEJMoa1504942
  66. Richards DB, Cookson LM, Barton SV, et al. Repeat doses of antibody to serum amyloid P component clear amyloid deposits in patients with systemic amyloidosis. Sci Transl Med. 2018;10(422):eaan3128. doi: 10.1126/scitranslmed.aan3128

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