graphic

Claudio Rapezzi passed away at the age of 71, leaving abruptly all his patients, friends, colleagues, and pupils. Rapezzi ‘was first and foremost a clinician who always put the patient first and could always be counted on to appropriately frame new discoveries’, as Frederick Ruberg wrote. He gave a substantial contribution to the advance in medical knowledge thanks to his unique qualities of curiosity, culture, and imaginative vision in each of the many fields his work touched: from the never-ending love for electrocardiography, manifested from his first publication1 up to its novel applications in cardiomyopathies, to the legacy he has left in cardiac amyloidosis with the ‘many ideas that we take for granted now, bone tracer cardiac imaging, tafamidis and so much more’, as Sharmila Dorbala has written, to the last Editorial on sex differences in this disease.2

Amyloid transthyretin cardiomyopathy (ATTR-CM) is emerging as an important cause of morbidity and mortality and a widely underdiagnosed disorder. One of the reasons for the recent interest on ATTR-CM is the availability of an algorithm for the non-invasive diagnosis of this condition. Indeed, the combination of an intense cardiac uptake of bone tracers and the absence of a monoclonal protein allows us to diagnose ATTR-CM without the need for the demonstration of amyloid deposits on tissue samples from the heart or an extracardiac site.1 In detail, cardiac uptake must be as intense as that of the sternum and ribs (Perugini Grade 2), or more intense than the sternum and ribs (Perugini Grade 3).3 The Perugini grading system is named after Enrica Perugini, the first author of a seminal paper published in 2005 by the research group from Bologna coordinated by Claudio Rapezzi.3 It was thus Prof. Rapezzi who introduced this very simple grading system and understood its relevance for the differential diagnosis between light-chain and ATTR-CM. Indeed, an international collaboration led by Rapezzi and the group of the National Amyloidosis Centre in London established in 2016 that ‘the combined findings of grade 2 or 3 myocardial radiotracer uptake on bone scintigraphy and the absence of a monoclonal protein in serum or urine had a specificity and positive predictive value for cardiac ATTR amyloidosis of 100%’,4 thus introducing the concept of a non-invasive diagnosis of ATTR-CM that is now adopted worldwide.5 Every diagnosis of ATTR-CM made without the need of a tissue biopsy is then an ideal tribute to the vision of Rapezzi. In the same years, the Phase 3 Safety and Efficacy of Tafamidis in Patients with Transthyretin Cardiomyopathy (ATTR-ACT) trial was evaluating the TTR stabilizer tafamidis in patients with ATTR-CM. The results of this trial, presented by Rapezzi during the 2018 European Society of Cardiology meeting in Munich, opened a new therapeutic avenue for patients with ATTR-CM from all over the world.6 Tafamidis still remains the only approved treatment for ATTR-CM, either variant or wild-type, with a demonstrated survival benefit confirmed even in a long-term extension study.7 Rapezzi also contributed greatly to spread the knowledge on ATTR-CM through multiple initiatives, ranging from a position statement of the European Society of Cardiology on the diagnosis and management of amyloid CM8 to other consensus documents,9–12 to talks and educational activities in many congresses, and the formation of many young clinicians and fellows, many of whom established new outpatient clinics devoted to amyloid CM.

Today we mourn a founding father of research on amyloid CM and a great educator, but also a curious individual with a broad range of interest ranging from the history of medicine to literature and arts. As Iacopo Olivotto said, ‘he was a friend and mentor to many, and the living proof that brilliance, genius and pleasantness may coexist. He was a unique human being who shed a light on everyone who crossed his path, with a smile’. We are close to his family and the cardiology community for the loss of an irreplaceable figure who has given prestige to the scientific community. We wish to conclude with the thought of Giampaolo Merlini: ‘We will miss him very much. There is the age of joy and there is the age of pain; only love remains’.

References

1

Labriola
E
,
Rapezzi
C
,
Ferlito
M
,
Sangiorgio
P
,
Addarii
F
,
Marlettini
MG
,
Fiori
W
.
Il vettorcardiogramma nell'infarto miocardico della parete diaframmatica ecgraficamente non riconoscibile [The vectorcardiogram in myocardial infarct of the diaphragmatic wall that is unrecognizable in the electrocardiogram]
.
Boll Soc Ital Cardiol
1977
;
22
:
1796
1802
.

2

Rapezzi
C
,
Emdin
M
,
Aimo
A
.
Unravelling the role of sex in the pathophysiology, phenotypic expression and diagnosis of cardiac amyloidosis
.
Eur J Heart Fail
;
doi: 10.1002/ejhf.2674. Published online ahead of print 4 September 2022
.

3

Perugini
E
,
Guidalotti
PL
,
Salvi
F
, Cooke RM, Pettinato C, Riva L, Leone O, Farsad M, Ciliberti P, Bacchi-Reggiani L, Fallani F, Branzi A, Rapezzi C
Noninvasive etiologic diagnosis of cardiac amyloidosis using 99mTc-3,3-diphosphono-1,2-propanodicarboxylic acid scintigraphy
.
J Am Coll Cardiol
2005
;
46
:
1076
1084
.

4

Gillmore
JD
,
Maurer
MS
,
Falk
RH
, Merlini G, Damy T, Dispenzieri A, Wechalekar AD, Berk JL, Quarta CC, Grogan M, Lachmann HJ, Bokhari S, Castano A, Dorbala S, Johnson GB, Glaudemans AW, Rezk T, Fontana M, Palladini G, Milani P, Guidalotti PL, Flatman K, Lane T, Vonberg FW, Whelan CJ, Moon JC, Ruberg FL, Miller EJ, Hutt DF, Hazenberg BP, Rapezzi C, Hawkins PN
Nonbiopsy diagnosis of cardiac transthyretin amyloidosis
.
Circulation
2016
;
133
:
2404
2412
.

5

Rapezzi
C
,
Aimo
A
,
Serenelli
M
, Barison A, Vergaro G, Passino C, Panichella G, Sinagra G, Merlo M, Fontana M, Gillmore J, Quarta CC, Maurer MS, Kittleson MM, Garcia-Pavia P, Emdin M
Critical comparison of documents from scientific societies on cardiac amyloidosis: JACC State-of-the-Art Review
.
J Am Coll Cardiol
2022
;
79
:
1288
1303
.

6

Maurer
MS
,
Schwartz
JH
,
Gundapaneni
B
, Elliott PM, Merlini G, Waddington-Cruz M, Kristen AV, Grogan M, Witteles R, Damy T, Drachman BM, Shah SJ, Hanna M, Judge DP, Barsdorf AI, Huber P, Patterson TA, Riley S, Schumacher J, Stewart M, Sultan MB, Rapezzi C; ATTR-ACT Study Investigators
Tafamidis treatment for patients with transthyretin amyloid cardiomyopathy
.
N Engl J Med
2018
;
379
:
1007
1016
.

7

Elliott
P
,
Drachman
BM
,
Gottlieb
SS
, Hoffman JE, Hummel SL, Lenihan DJ, Ebede B, Gundapaneni B, Li B, Sultan MB, Shah SJ
Long-term survival with tafamidis in patients with transthyretin amyloid cardiomyopathy
.
Circ Heart Fail
2022
;
15
:
e008193
.

8

Garcia-Pavia
P
,
Rapezzi
C
,
Adler
Y
, Arad M, Basso C, Brucato A, Burazor I, Caforio ALP, Damy T, Eriksson U, Fontana M, Gillmore JD, Gonzalez-Lopez E, Grogan M, Heymans S, Imazio M, Kindermann I, Kristen AV, Maurer MS, Merlini G, Pantazis A, Pankuweit S, Rigopoulos AG, Linhart A
Diagnosis and treatment of cardiac amyloidosis: a position statement of the ESC Working Group on Myocardial and Pericardial Diseases
.
Eur Heart J
2021
;
42
:
1554
1568
.

9

Elliott
P
,
Drachman
BM
,
Gottlieb
SS
, Hoffman JE, Hummel SL, Lenihan DJ, Ebede B, Gundapaneni B, Li B, Sultan MB, Shah SJ
Long-term survival with tafamidis in patients with transthyretin amyloid cardiomyopathy
.
Circ Heart Fail
2022
;
15
:
e008193
.

10

Dorbala
S
,
Ando
Y
,
Bokhari
S
, Dispenzieri A, Falk RH, Ferrari VA, Fontana M, Gheysens O, Gillmore JD, Glaudemans AWJM, Hanna MA, Hazenberg BPC, Kristen AV, Kwong RY, Maurer MS, Merlini G, Miller EJ, Moon JC, Murthy VL, Quarta CC, Rapezzi C, Ruberg FL, Shah SJ, Slart RHJA, Verberne HJ, Bourque JM
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
.
Circ Cardiovasc Imaging
2021
;
14
:
e000029
.

11

Dorbala
S
,
Ando
Y
,
Bokhari
S
, Dispenzieri A, Falk RH, Ferrari VA, Fontana M, Gheysens O, Gillmore JD, Glaudemans AWJM, Hanna MA, Hazenberg BPC, Kristen AV, Kwong RY, Maurer MS, Merlini G, Miller EJ, Moon JC, Murthy VL, Quarta CC, Rapezzi C, Ruberg FL, Shah SJ, Slart RHJA, Verberne HJ, Bourque JM
ASNC/AHA/ASE/EANM/HFSA/ISA/SCMR/SNMMI expert consensus recommendations for multimodality imaging in cardiac amyloidosis: part 2 of 2-diagnostic criteria and appropriate utilization
.
Circ Cardiovasc Imaging
2021
;
14
:
e000030
.

12

Garcia-Pavia
P
,
Bengel
F
,
Brito
D
, Damy T, Duca F, Dorbala S, Nativi-Nicolau J, Obici L, Rapezzi C, Sekijima Y, Elliott PM
Expert consensus on the monitoring of transthyretin amyloid cardiomyopathy
.
Eur J Heart Fail
2021
;
23
:
895
905
.

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