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Incidence, clinical characteristics, and diagnostic approach in transthyretin amyloid cardiomyopathy: The Kumamoto Cardiac Amyloidosis Survey.
Takashio, Seiji; Tokitsu, Takanori; Matsukawa, Masakazu; Sakaino, Naritsugu; Fujimoto, Kazuteru; Sakamoto, Tomohiro; Noda, Katsuo; Tsunoda, Ryusuke; Misumi, Ikuo; Hirai, Nobutaka; Doi, Hideki; Koide, Shunichi; Mizuno, Yuji; Hirose, Toyoki; Kurokawa, Hirofumi; Kajiwara, Ichiro; Ohba, Keisuke; Miyamoto, Shinzo; Araki, Satoshi; Yamamoto, Eiichiro; Matsushita, Kenichi; Ueda, Mitsuharu; Tsujita, Kenichi.
Afiliação
  • Takashio S; Department of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan. Electronic address: s-takash@kumamoto-u.ac.jp.
  • Tokitsu T; Division of Cardiology, Kumamoto Kenhoku Hospital, Tamana, Japan.
  • Matsukawa M; Division of Cardiology, Kumamoto Kenhoku Hospital, Tamana, Japan.
  • Sakaino N; Division of Cardiology, Amakusa Medical Center, Amakusa, Japan.
  • Fujimoto K; Division of Cardiology, National Hospital Organization Kumamoto Medical Center, Kumamoto, Japan.
  • Sakamoto T; Division of Cardiology, Saiseikai Kumamoto Hospital Cardiovascular Center, Kumamoto, Japan.
  • Noda K; Division of Cardiology, Kumamoto Central Hospital, Kumamoto, Japan.
  • Tsunoda R; Division of Cardiology, Japanese Red Cross Kumamoto Hospital, Kumamoto, Japan.
  • Misumi I; Division of Cardiology, Kumamoto City Hospital, Kumamoto, Japan.
  • Hirai N; Division of Cardiology, Kumamoto Regional Medical Center, Kumamoto, Japan.
  • Doi H; Division of Cardiology, Japan Labor Health and Welfare Organization Kumamoto Rosai Hospital, Yatsushiro, Japan.
  • Koide S; Division of Cardiology, Japan Community Health Care Organization Kumamoto General Hospital, Yatsushiro, Japan.
  • Mizuno Y; Division of Cardiovascular Medicine, Kumamoto Kinoh Hospital/Kumamoto Aging Research Institute, Kumamoto, Japan.
  • Hirose T; Division of Cardiology, Minamata City General Hospital and Medical Center, Minamata, Japan.
  • Kurokawa H; Division of Cardiology, Japan Community Health Care Organization Hitoyoshi Medical Center, Hitoyoshi, Japan.
  • Kajiwara I; Division of Cardiology, Arao Municipal Hospital, Arao, Japan.
  • Ohba K; Division of Cardiology, Yamaga Medical Center, Yamaga, Japan.
  • Miyamoto S; Division of Cardiology, Aso Medical Center, Aso, Japan.
  • Araki S; Department of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
  • Yamamoto E; Department of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
  • Matsushita K; Department of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
  • Ueda M; Department of Neurology, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
  • Tsujita K; Department of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University, Kumamoto, Japan.
J Cardiol ; 80(1): 49-55, 2022 07.
Article em En | MEDLINE | ID: mdl-35078683
ABSTRACT

BACKGROUND:

In recent years, transthyretin amyloid cardiomyopathy (ATTR-CM) has received increasing attention; however, the epidemiology of ATTR-CM in Japan is not yet understood. In the Kumamoto Cardiac Amyloid Survey, we evaluated the current incidence, clinical characteristics, diagnostic approaches, and treatment strategies for ATTR-CM and compared tafamidis-prescription hospitals with regional hospitals.

METHODS:

We conducted a retrospective multicenter observational cohort study. The registry included patients with ATTR-CM diagnosed in two tafamidis-prescription hospital institutes [Japanese Circulation Society (JCS)-certified facilities] and 15 regional cardiovascular facilities in Kumamoto between January 2018 and December 2020.

RESULTS:

In total, 174 patients were diagnosed with ATTR-CM. The incidence of ATTR-CM was estimated to be approximately 1 per 10,000 person-years in the elderly population (>65 years old) in Kumamoto. Compared with that in the JCS-certified facilities cohort (n=115), age at diagnosis was significantly older (84.5 ± 5.6 vs. 77.5 ± 6.3 years old; p<0.01) in the regional hospitals cohort (n=59). Histological (25% vs. 81%; p<0.01) and genetic diagnosis (7% vs. 82%) were also less frequently performed. Probable (as indicated by positive bone scintigraphy findings with confirmation of monoclonal protein absence) and possible (as indicated by positive bone scintigraphy findings without confirmation of monoclonal protein absence) ATTR-CM accounted for the majority of cases (75% vs. 19%; p<0.01) in the regional hospitals cohort compared to the JCS-certified facilities cohort. There were no cases of hereditary ATTR-CM among the patients who underwent TTR genetic testing (n=98).

CONCLUSIONS:

We confirmed the incidence of ATTR-CM in Kumamoto and the diagnostic approach used in patients with ATTR-CM. Further prospective studies with a larger sample are needed to validate our results and to further shed light on the epidemiology of ATTR-CM in Japan.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neuropatias Amiloides Familiares / Cardiomiopatias Tipo de estudo: Clinical_trials / Diagnostic_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Humans Idioma: En Revista: J Cardiol Assunto da revista: CARDIOLOGIA Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neuropatias Amiloides Familiares / Cardiomiopatias Tipo de estudo: Clinical_trials / Diagnostic_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Aged80 / Humans Idioma: En Revista: J Cardiol Assunto da revista: CARDIOLOGIA Ano de publicação: 2022 Tipo de documento: Article