AMYLOID-JOURNAL OF PROTEIN FOLDING DISORDERS

A collaborative approach to amyloidosis and a multidisciplinary care framework - position statement from the International Society of Amyloidosis
Sanchorawala V, Wechalekar A, Mollee P, Sekijima Y, Maurer MS, Leung N, Schönland SO and Kumar S
Change of guard at - a tribute to outgoing Editor in Chief, Professor Per Westermark
Kumar S
Commentary to revisiting the genetic epidemiology of ATTRv in Spain: the Balearic Islands as a high-prevalence founder focus
Domínguez-Martínez M, Caro-Llopis A and Orellana C
Single-slide detection and typing of AL renal amyloidosis: combining mass spectrometry imaging and digital pathology
Bindi G, Cazzaniga G, Alberici F, Mescia F, Mannino M, Maggioni A, Galimberti S, Capitoli G, Fisogni S, Magni F, Pagni F, Smith A and L'Imperio V
Amyloid typing, particularly in monoclonal gammopathies of renal significance, can be technically challenging. Matrix-Assisted Laser Desorption/Ionisation-Mass Spectrometry Imaging (MALDI-MSI) has been proposed as a non-destructive method to detect and type amyloid deposits on a single tissue slide. This study aims to confirm this capability of MALDI-MSI in renal light chain amyloidosis (AL amyloidosis), irrespective of the fixative utilised, confronting results with other traditional and upcoming methods for amyloid detection.
Revisiting the genetic epidemiology of ATTRv in Spain: the Balearic Islands as a high-prevalence founder focus
Ventayol-Guirado M, Cisneros-Barroso E, Ribot-Sansó MA, González-Moreno J, Losada I, Ripoll-Vera T, Pons J, Fortuny E, Bosch T, Figuerola A, Descals C, Montala JC, Álvarez-Rubio J, Hernández-Rodríguez J, Lustre-Rodríguez J, Llull-Alberti MV, Jiménez-Barceló JA, Asensio-Landa VJ, Torres-Juan L, Martínez-López I, Buades-Reines J and Heine-Suñer D
Frontline Dara-CyBorD for AL amyloidosis: high response rates and cytogenetic insights from a real-world cohort
Wu X, Brailovski E, Toskic D, Scalia S, Zhou P, Ma X, Mico V, Fogaren T, Lyons NC, Landau H and Comenzo R
Interactions between amyloid fibril proteins
Westermark P
An Accelerated Sonication-Assisted Preparation method for mass spectrometry-based identification of subtype specific amyloidogenic proteins in fat aspirates
Palstrøm NB, Lindegaard CA, Rojek A, Campbell AJ, Toftmann Hansen C, Møller HEH, Abildgaard N and Beck HC
Cardiac Phenotype and Clinical Outcomes in Randall Disease versus Light-Chain Amyloidosis
Nicol M, Cohen C, Talbot A, Baudet M, Harel S, Forgeard N, Royer B, Theves F, Vaugeois T, Logeart D and Arnulf B
AA amyloidosis as an adverse event of immune checkpoint inhibitor therapy: evidence from the FDA adverse event reporting system and a systematic review
Topcu U, Esen BH, Bektas SN, Selçukbiricik F and Kanbay M
Immune checkpoint inhibitors (ICIs) have transformed cancer therapy but are linked to immune-related adverse events (irAEs). Secondary (AA) amyloidosis, an inflammatory complication involving serum amyloid A deposition, has been sporadically reported in ICI-treated patients. We investigated the link between ICI therapy and AA amyloidosis using pharmacovigilance data and a systematic review.
Optimized methods for efficient application of immunogold electron microscopy to amyloid fibrils typing
Zhou Y, Lu W, Burks E, Henderson JM, Andry C, Sanchorawala V, Sheikh Z, Prokaeva TB and Chen HA
Amyloidosis is a group of disorders characterized by aggregation of abnormal amyloid protein in various tissues, often leading to organ dysfunction and failure. We optimized the immunogold electron microscopy (IEM) technique to enable efficient amyloid typing in 4% paraformaldehyde-fixed (PFA) and formalin-fixed paraffin-embedded (FFPE) tissues.
Limited diagnostic utility of systematic Congo red staining in bone marrow biopsies
Haugbølle Bjerre J
Clinical profile and outcome of AA amyloidosis associated kidney disease in India
Bansal B, Sarkar A, Barwad A, Singh G, Subbiah A, Yadav RK, Mahajan S, Bhowmik D, Agarwal SK and Bagchi S
AA amyloidosis is a rare but significant cause of chronic kidney disease (CKD). We aimed to characterize the clinical profile of patients with AA amyloidosis affecting the kidneys in the Indian subcontinent.
Failure to screen for monoclonal proteins in patients who undergo bone scintigraphy for suspected cardiac amyloidosis
Devine A, Selland A, Arriola-Montenegro J and Maharaj V
A comparison of single versus combination mechanism treatment for transthyretin amyloid cardiomyopathy
Gupta V, Yanek LR, Shankar B, Jefferson A, Tsottles D, Zampino S, Barranco J, Rahim M, Brown E, Ranek M, Gilotra N, Sharma K, Polydefkis M and Vaishnav J
Tafamidis treatment and neuropsychiatric dysfunction in patients with cardiac aTTR: a post-hoc analysis of the ATTRACT trial
Steafo L, Zubair U, George J and Skaistis J
Neuropathy impairment and nutritional status with eplontersen in patients with hereditary transthyretin-mediated amyloidosis
Wixner J, Conceição I, Berk JL, Adams D, Polydefkis MJ, Attarian S, Gillmore JD, Dyck PJB, Chen J, Kwoh TJ, Nåtman J, Zhou W and Cruz MW
Cold pressor test and paradoxical blood pressure reduction in light chain amyloidosis
Patras R, Georgiopoulos G, Theodorakakou F, Petropoulos I, Delialis D, Angelidakis L, Briasoulis A, Gavriatopoulou M, Kokotis P, Manios E, Dimopoulos MA, Kastritis E and Stamatelopoulos K
Patients with AL amyloidosis present sustained paradoxical vasodilation in response to sympathetic stimulation by cold pressor test (CPT). The clinical relevance is unknown.
Bile cast nephropathy presenting as acute kidney injury in systemic light chain amyloidosis with severe hepatic involvement
Garza-Morales R, Fu L, Rosenthal JL and Yadav U
Amyloid myopathy in the internal oblique muscle of patients with wild-type transthyretin cardiac amyloidosis
Takahashi K, Iwamura T, Hiratsuka Y, Yamamoto S, Sasaki D, Kitazawa S, Yamamura N, Ueda M, Morioka H, Uemura S, Sakaue T and Inoue K
Clinical and radiological stabilization following vutrisiran treatment in transthyretin leptomeningeal amyloidosis: a case report
Rossi S, Spinardi L, Guaraldi P, Mastrangelo A, Riefolo M, Vaisfeld A, Palombo F, Longhi S, Rinaldi R, Conti A, Foschini MP and Guarino M