Literature DB >> 34690220

Prospective Registry Study of Primary Dyslipidemia (PROLIPID): Rationale and Study Design.

Hayato Tada1, Tomoyuki Kurashina2, Masatsune Ogura3, Misa Takegami4, Yoshihiro Miyamoto5, Hidenori Arai6, Mariko Harada-Shiba7, Shun Ishibashi2.   

Abstract

INTRODUCTION: Primary dyslipidemias are inherited disorders in plasma lipoprotein metabolism that lead to serious cardiovascular and other complications. The Japanese Ministry of Health, Labor and Welfare (MHLW) covers medical expenses, under the Research Program on Rare and Intractable Diseases, for homozygous familial hypercholesterolemia (FH), familial chylomicronemia, sitosterolemia, cerebrotendinous xanthomatosis, lecithin:cholesterol acyltransferase deficiency, Tangier disease, and abetalipoproteinemia. Apolipoprotein A1 deficiency, heterozygous FH, and type III hyperlipoproteinemia are covered by the MHLW Pediatric Chronic Disease Program. Heterozygous FH and type III hyperlipoproteinemia are also important for their relatively common prevalence and, accordingly, high impact on Japanese public health by significant contribution to the overall prevalence of cardiovascular diseases. Therefore, a systemic survey of these diseases is mandatory to estimate their actual situation, such as prevalence, clinical manifestations, and prognoses among the Japanese population. The impact of these rare and intractable diseases on cardiovascular and other complications will likely be higher among Japanese people than other ethnicities because the general Japanese population has many cardioprotective aspects. The current study intends to conduct a multicenter registry of these diseases to assess their demographics and clinical features comprehensively. METHODS AND ANALYSIS: The Prospective Registry Study of Primary Dyslipidemia is a registry-based prospective, observational, multicenter cohort study in Japan, enrolling patients who fulfill the Japanese clinical criteria of the primary dyslipidemias listed above, from 26 participating institutes from August 2015 to March 2023. A total of 1,000 patients will be enrolled in the study and followed for 10 years. Clinical parameters are collected, including physical and laboratory findings, genetic analysis, drugs, lifestyle management, and clinical events, especially cardiovascular events. The primary endpoint of this study is the new onset of cardiovascular disease and acute pancreatitis, and the secondary endpoint is death from any causes. ETHICS AND DISSEMINATION: This study complies with the Declaration of Helsinki, the Ethical Guidelines for Medical and Health Research Involving Human Subjects, and all other applicable laws and guidelines in Japan. The institutional review boards have approved this study protocol at all participating institutes. The final results are to be published at appropriate international conferences and in peer-reviewed journals.

Entities:  

Keywords:  Dyslipidemia; Genetics; Intractable disease; Registry

Mesh:

Year:  2021        PMID: 34690220      PMCID: PMC9174082          DOI: 10.5551/jat.63222

Source DB:  PubMed          Journal:  J Atheroscler Thromb        ISSN: 1340-3478            Impact factor:   4.394


  28 in total

1.  Predicting Cardiovascular Events in Familial Hypercholesterolemia: The SAFEHEART Registry (Spanish Familial Hypercholesterolemia Cohort Study).

Authors:  Leopoldo Pérez de Isla; Rodrigo Alonso; Nelva Mata; Cristina Fernández-Pérez; Ovidio Muñiz; José Luis Díaz-Díaz; Adriana Saltijeral; Francisco Fuentes-Jiménez; Raimundo de Andrés; Daniel Zambón; Mar Piedecausa; José María Cepeda; Marta Mauri; Jesús Galiana; Ángel Brea; Juan Francisco Sanchez Muñoz-Torrero; Teresa Padró; Rosa Argueso; José Pablo Miramontes-González; Lina Badimón; Raúl D Santos; Gerald F Watts; Pedro Mata
Journal:  Circulation       Date:  2017-03-08       Impact factor: 29.690

2.  Prevalence of Familial Hypercholesterolemia Among the General Population and Patients With Atherosclerotic Cardiovascular Disease: A Systematic Review and Meta-Analysis.

Authors:  Pengwei Hu; Kanika I Dharmayat; Kausik K Ray; Antonio J Vallejo-Vaz; Christophe A T Stevens; Mansour T A Sharabiani; Rebecca S Jones; Gerald F Watts; Jacques Genest
Journal:  Circulation       Date:  2020-05-29       Impact factor: 29.690

3.  Worldwide Prevalence of Familial Hypercholesterolemia: Meta-Analyses of 11 Million Subjects.

Authors:  Sabina O Beheshti; Christian M Madsen; Anette Varbo; Børge G Nordestgaard
Journal:  J Am Coll Cardiol       Date:  2020-05-26       Impact factor: 24.094

4.  A novel homozygous missense mutation in the apo A-I gene with apo A-I deficiency.

Authors:  W Huang; J Sasaki; A Matsunaga; H Nanimatsu; K Moriyama; H Han; M Kugi; T Koga; K Yamaguchi; K Arakawa
Journal:  Arterioscler Thromb Vasc Biol       Date:  1998-03       Impact factor: 8.311

5.  Molecular genetic epidemiology of homozygous familial hypercholesterolemia in the Hokuriku district of Japan.

Authors:  Hiroshi Mabuchi; Atsushi Nohara; Tohru Noguchi; Junji Kobayashi; Masa-Aki Kawashiri; Hayato Tada; Chiaki Nakanishi; Mika Mori; Masakazu Yamagishi; Akihiro Inazu; Junji Koizumi
Journal:  Atherosclerosis       Date:  2010-11-13       Impact factor: 5.162

6.  Mutations in Japanese subjects with primary hyperlipidemia--results from the Research Committee of the Ministry of Health and Welfare of Japan since 1996--.

Authors:  Takao Maruyama; Shizuya Yamashita; Yuji Matsuzawa; Hideaki Bujo; Kazuo Takahashi; Yasushi Saito; Shun Ishibashi; Ken Ohashi; Futoshi Shionoiri; Takanari Gotoda; Nobuhiro Yamada; Toru Kita
Journal:  J Atheroscler Thromb       Date:  2004       Impact factor: 4.928

7.  Prognostic impact of cascade screening for familial hypercholesterolemia on cardiovascular events.

Authors:  Hayato Tada; Hirofumi Okada; Akihiro Nomura; Atsushi Nohara; Masakazu Yamagishi; Masayuki Takamura; Masa-Aki Kawashiri
Journal:  J Clin Lipidol       Date:  2021-01-04       Impact factor: 4.766

Review 8.  Homozygous Familial Hypercholesterolemia.

Authors:  Atsushi Nohara; Hayato Tada; Masatsune Ogura; Sachiko Okazaki; Koh Ono; Hitoshi Shimano; Hiroyuki Daida; Kazushige Dobashi; Toshio Hayashi; Mika Hori; Kota Matsuki; Tetsuo Minamino; Shinji Yokoyama; Mariko Harada-Shiba
Journal:  J Atheroscler Thromb       Date:  2021-04-18       Impact factor: 4.928

Review 9.  Current Diagnosis and Management of Tangier Disease.

Authors:  Masahiro Koseki; Shizuya Yamashita; Masatsune Ogura; Yasushi Ishigaki; Koh Ono; Kazuhisa Tsukamoto; Mika Hori; Kota Matsuki; Shinji Yokoyama; Mariko Harada-Shiba
Journal:  J Atheroscler Thromb       Date:  2021-05-14       Impact factor: 4.928

Review 10.  Diagnosis and Management of Sitosterolemia 2021.

Authors:  Hayato Tada; Akihiro Nomura; Masatsune Ogura; Katsunori Ikewaki; Yasushi Ishigaki; Kyoko Inagaki; Kazuhisa Tsukamoto; Kazushige Dobashi; Kimitoshi Nakamura; Mika Hori; Kota Matsuki; Shizuya Yamashita; Shinji Yokoyama; Masa-Aki Kawashiri; Mariko Harada-Shiba
Journal:  J Atheroscler Thromb       Date:  2021-04-28       Impact factor: 4.928

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