Estimating the Prevalence of Transthyretin Amyloid Cardiomyopathy in a Large In-Hospital Database in Japan

被引:38
作者
Winburn, Ian [1 ]
Ishii, Tomonori [2 ]
Sumikawa, Takuma [2 ]
Togo, Kanae [2 ]
Yasunaga, Hideo [3 ]
机构
[1] Pfizer, Walton Oaks, England
[2] Pfizer Japan Inc, Tokyo, Japan
[3] Univ Tokyo, Sch Publ Hlth, Dept Clin Epidemiol & Hlth Econ, Tokyo, Japan
关键词
Amyloidosis; Cardiomyopathy; Japan; Observational study; WILD-TYPE TRANSTHYRETIN; HEART-FAILURE; CARDIAC AMYLOIDOSIS; DIAGNOSIS; PHENOTYPE;
D O I
10.1007/s40119-019-0142-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Transthyretin amyloid cardiomyopathy (ATTR-CM)-a debilitating, fatal disease resulting from the deposition of transthyretin (TTR) amyloid fibrils-can be hereditary due to mutations in the TTR gene (ATTRm) or wild type (ATTRwt). The global prevalence of ATTR-CM is largely unknown, although likely underestimated, with no formal epidemiological prevalence studies in Japan. This study aimed to estimate the prevalence of ATTR-CM in a large in-hospital database in Japan. Methods: This was a retrospective, observational, cross-sectional study which utilized data from all adult patients (aged >= 20 years) in the hospital-based Japan Medical Data Vision (MDV) database from January 2010 to September 2018 to estimate the number of currently diagnosed ATTR-CM patients and describe their demographic and clinical characteristics and diagnostic modalities. ATTR-CM patients (ATTRwt and ATTRm) were identified using a range of diagnosis codes that were applied to create broad and narrow definitions of the disease. Results: Over the 9 years of this study, there were 3255 (155.8 per million adult patients in the MDV database) to 3992 (191.1 per million) diagnoses of ATTRwt and 67 (3.2 per million) to 106 (5.1 per million) diagnoses of ATTRm in the MDV database (based on the narrow and broad definitions, respectively). There were 444 (21.2 per million) diagnoses of amyloid light-chain (AL) amyloidosis. Considering only those patients who were also diagnosed with heart failure, there were 1468 (70.3 per million) to 1798 (86.1 per million) diagnoses of ATTRwt and 50 (2.4 per million) to 61 (2.9 per million) diagnoses of ATTRm. Most ATTRwt patients (similar to 90%) did not have a record of endomyocardial or abdominal wall biopsy, or of scintigram. Conclusion: This retrospective study provides an estimate of the number of patients diagnosed with ATTR-CM in a large in-hospital database in Japan over a period of 9 years. Improving awareness of disease prevalence may improve diagnosis and treatment.
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页码:297 / 316
页数:20
相关论文
共 23 条
[1]   Unveiling transthyretin cardiac amyloidosis and its predictors among elderly patients with severe aortic stenosis undergoing transcatheter aortic valve replacement [J].
Castano, Adam ;
Narotsky, David L. ;
Hamid, Nadira ;
Khalique, Omar K. ;
Morgenstern, Rachelle ;
DeLuca, Albert ;
Rubin, Jonah ;
Chiuzan, Codruta ;
Nazif, Tamim ;
Vahl, Torsten ;
George, Isaac ;
Kodali, Susheel ;
Leon, Martin B. ;
Hahn, Rebecca ;
Bokhari, Sabahat ;
Maurer, Mathew S. .
EUROPEAN HEART JOURNAL, 2017, 38 (38) :2879-2887
[2]   Heart Failure Resulting From Age-Related Cardiac Amyloid Disease Associated With Wild-Type Transthyretin A Prospective, Observational Cohort Study [J].
Connors, Lawreen H. ;
Sam, Flora ;
Skinner, Martha ;
Salinaro, Francesco ;
Sun, Fangui ;
Ruberg, Frederick L. ;
Berk, John L. ;
Seldin, David C. .
CIRCULATION, 2016, 133 (03) :282-290
[3]   Transthyretin cardiac amyloidosis in continental Western Europe: an insight through the Transthyretin Amyloidosis Outcomes Survey (THAOS) [J].
Damy, Thibaud ;
Kristen, Arnt, V ;
Suhr, Ole B. ;
Maurer, Mathew S. ;
Plante-Bordeneuve, Violaine ;
Yu, Ching-Ray ;
Ong, Moh-Lim ;
Coelho, Teresa ;
Rapezzi, Claudio .
EUROPEAN HEART JOURNAL, 2022, 43 (05) :391-400
[4]   Prevalence and clinical phenotype of hereditary transthyretin amyloid cardiomyopathy in patients with increased left ventricular wall thickness [J].
Damy, Thibaud ;
Costes, Bruno ;
Hagege, Albert A. ;
Donal, Erwan ;
Eicher, Jean-Christophe ;
Slama, Michel ;
Guellich, Aziz ;
Rappeneau, Stephane ;
Gueffet, Jean-Pierre ;
Logeart, Damien ;
Plante-Bordeneuve, Violaine ;
Bouvaist, Helene ;
Huttin, Olivier ;
Mulak, Genevieve ;
Dubois-Rande, Jean-Luc ;
Goossens, Michel ;
Canoui-Poitrine, Florence ;
Buxbaum, Joel N. .
EUROPEAN HEART JOURNAL, 2016, 37 (23) :1826-1834
[5]   2014 ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy The Task Force for the Diagnosis and Management of Hypertrophic Cardiomyopathy of the European Society of Cardiology (ESC) [J].
Elliott, Perry M. ;
Anastasakis, Aris ;
Borger, Michael A. ;
Borggrefe, Martin ;
Cecchi, Franco ;
Charron, Philippe ;
Hagege, Albert Alain ;
Lafont, Antoine ;
Limongelli, Giuseppe ;
Mahrholdt, Heiko ;
McKenna, William J. ;
Mogensen, Jens ;
Nihoyannopoulos, Petros ;
Nistri, Stefano ;
Pieper, Petronella G. ;
Pieske, Burkert ;
Rapezzi, Claudio ;
Rutten, Frans H. ;
Tillmanns, Christoph ;
Watkins, Hugh .
EUROPEAN HEART JOURNAL, 2014, 35 (39) :2733-+
[6]   Diagnosis, Prognosis, and Therapy of Transthyretin Amyloidosis [J].
Gertz, Morie A. ;
Benson, Merrill D. ;
Dyck, Peter J. ;
Grogan, Martha ;
Coelho, Terresa ;
Cruz, Marcia ;
Berk, John L. ;
Plante-Bordeneuve, Violaine ;
Schmidt, Hartmut H. J. ;
Merlini, Giampaolo .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2015, 66 (21) :2451-2466
[7]   Clinical characteristics of wild-type transthyretin cardiac amyloidosis: disprovingmyths [J].
Gonzalez-Lopez, Esther ;
Gagliardi, Christian ;
Dominguez, Fernando ;
Quarta, Cristina Candida ;
Javier de Haro-del Moral, F. ;
Milandri, Agnese ;
Salas, Clara ;
Cinelli, Mario ;
Cobo-Marcos, Marta ;
Lorenzini, Massimiliano ;
Lara-Pezzi, Enrique ;
Foffi, Serena ;
Alonso-Pulpon, Luis ;
Rapezzi, Claudio ;
Garcia-Pavia, Pablo .
EUROPEAN HEART JOURNAL, 2017, 38 (24) :1895-1904
[8]   Wild-type transthyretin amyloidosis as a cause of heart failure with preserved ejection fraction [J].
Gonzalez-Lopez, Esther ;
Gallego-Delgado, Maria ;
Guzzo-Merello, Gonzalo ;
de Haro-del Moral, F. Javier ;
Cobo-Marcos, Marta ;
Robles, Carolina ;
Bornstein, Belen ;
Salas, Clara ;
Lara-Pezzi, Enrique ;
Alonso-Pulpon, Luis ;
Garcia-Pavia, Pablo .
EUROPEAN HEART JOURNAL, 2015, 36 (38) :2585-2594
[9]   Hospital Volume and Cardiac Complications of Endomyocardial Biopsy: A Retrospective Cohort Study of 9508 Adult Patients Using a Nationwide Inpatient Database in Japan [J].
Isogai, Toshiaki ;
Yasunaga, Hideo ;
Matsui, Hiroki ;
Ueda, Tetsuro ;
Tanaka, Hiroyuki ;
Horiguchi, Hiromasa ;
Fushimi, Kiyohide .
CLINICAL CARDIOLOGY, 2015, 38 (03) :164-170
[10]   Recent advances in diagnosis and treatment of cardiac amyloidosis [J].
Izumiya, Yasuhiro ;
Takashio, Seiji ;
Oda, Seitaro ;
Yamashita, Yasuyuki ;
Tsujita, Kenichi .
JOURNAL OF CARDIOLOGY, 2018, 71 (1-2) :135-143