Masataka Yoshinaga
Fujita Health University
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Featured researches published by Masataka Yoshinaga.
International Heart Journal | 2015
Masataka Yoshinaga; Daiji Yoshikawa; Hideki Ishii; Akihiro Hirashiki; Takahiro Okumura; Aki Kubota; Shinichi Sakai; Ken Harada; Fuji Somura; Tomofumi Mizuno; Wakaya Fujiwara; Hiroatsu Yokoi; Mutsuharu Hayashi; Junichi Ishii; Yukio Ozaki; Toyoaki Murohara; Yukihiko Yoshida; Tetsuya Amano; Hideo Izawa
Hypertrophic cardiomyopathy (HCM) has various morphological and clinical features. A decade has passed since the previous survey of the epidemiological and clinical characteristics of Japanese HCM patients. The Aichi Hypertrophic Cardiomyopathy (AHC) Registry is based on a prospective multicenter observational study of HCM patients. The clinical characteristics of 42 ambulant HCM patients followed up for up to 5 years were investigated. The primary endpoint was major adverse cardiac events (MACE), defined as death, non-fatal stroke, admission due to congestive heart failure (CHF), or episodes of sustained ventricular tachycardia/fibrillation. The MACE-free survival during the 5-year follow-up period was 76% according to Kaplan-Meier analysis. HCM-related death occurred in 3 (7%) patients and SCD occurred in 2 (5%) patients. Additionally, 3 (7%) patients were admitted to the hospital due to CHF. Meanwhile, sustained VT was detected in one (2%) of the patients who received ICD implantation and subsequently terminated with antitachycardia pacing using an ICD. The patients with HCM exhibiting left ventricular outflow obstruction (HOCM) had a slightly lower MACE-free survival rate than those with neither HOCM nor dilated-HCM (dHCM) (71% versus 81%, log-rank P = 0.581). Furthermore, the patients with dHCM demonstrated a significantly lower MACE-free survival rate than those with neither HOCM nor dHCM (33% versus 81%, log-rank P = 0.029). In the AHC Registry targeting current Japanese HCM patients, we demonstrated that many HCM patients continue to suffer from MACE despite the development of various treatments for HCM.
Internal Medicine | 2015
Tomohito Kamada; Mutsuharu Hayashi; Hiroatsu Yokoi; Wakaya Fujiwara; Daiji Yoshikawa; Daisuke Mukaide; Yoshinori Sugishita; Masataka Yoshinaga; Takehiro Ito; Yukio Ozaki; Hideo Izawa
Takotsubo cardiomyopathy is a disorder characterized by left ventricular apical ballooning with preceding emotional and/or physical stressors. This condition is also an important differential diagnosis of acute coronary syndrome. We herein describe a case of Takotsubo cardiomyopathy, a significant clinical phenomenon, triggered by delayed-onset rhabdomyolysis following the administration of long-term statin treatment, without any preceding stressors or changes in the patients medical condition, in association with complaints of non-specific muscle-related symptoms. Although an electrocardiogram showed remarkable ST-segment elevation, a careful reading of the electrocardiogram findings revealed the features of Takotsubo cardiomyopathy. Withdrawing the statin therapy improved the patients cardiac function.
Journal of Cardiology | 2018
Wakaya Fujiwara; Yasuchika Kato; Mutsuharu Hayashi; Yoshinori Sugishita; Satoshi Okumura; Masataka Yoshinaga; Tomoya Ishiguro; Ryo Yamada; Masahide Harada; Hiroyuki Naruse; Junnichi Ishii; Yukio Ozaki; Hideo Izawa
BACKGROUND Although cardiac sarcoidosis is associated with poor prognosis, diagnosis of the disease is challenging and the sensitivity and specificity of diagnostic modalities are limited. This study was performed to evaluate the potential of serum microRNAs (miRNAs) as diagnostic biomarkers for cardiac sarcoidosis. METHODS We performed genome-wide expression profiling for 2565 miRNAs (Human-miRNA ver.21) using peripheral blood samples from 5 patients with cardiac sarcoidosis (61±9 years) and 3 healthy controls (54±7 years). From this screening study, we selected 12 miRNAs that were significantly related to cardiac sarcoidosis. Next, we performed real-time polymerase chain reaction (PCR) on blood samples from 15 new patients with cardiac sarcoidosis and 4 healthy controls to quantify the expression of these 12 miRNAs. RESULTS In the screening study, 12 miRNAs were differentially expressed (p<0.01) in all 5 patients with cardiac sarcoidosis, showing greater fold-change values (>4 or <0.25) compared with the expression in the 3 healthy controls. Analysis of the real-time PCR for blood samples from the other 15 patients and 4 controls using Mann-Whitney U tests revealed that the expression of miR-126 and miR-223 was significantly higher in the patients than in the healthy individuals. However, there were no differences in the expressions of miRNA-126 and miR-223 between patients with only cardiac lesions and those with extra-cardiac lesions. CONCLUSIONS Our results demonstrate the potential of serum miR-126 and miR-223 as new-generation biomarkers for the differential diagnosis of cardiac sarcoidosis in patients with heart failure.
Drug and Chemical Toxicology | 2017
Tomohito Kamada; Mutsuharu Hayashi; Wakaya Fujiwara; Daiji Yoshikawa; Daisuke Mukaide; Yoshinori Sugishita; Masataka Yoshinaga; Takehiro Itoh; Hiroatsu Yokoi; Junichi Ishii; Eiichi Watanabe; Yukio Ozaki; Hideo Izawa
Abstract Objectives: The number of elderly patients with hypertension has been steadily increasing. However, there are limited data on the safety and efficacy of the new angiotensin type 1 receptor blocker (ARB) azilsartan in elderly patients with hypertension. We investigated the clinical efficacy and safety of azilsartan in this population. Methods: The study population comprised 56 ambulatory patients with essential hypertension. We evaluated the reduction in blood pressure and safety after 12 weeks of treatment with azilsartan in 29 hypertensive patients ≥65 years of age (aged group) in comparison with the findings in 27 patients <65 years of age (non-aged group). Results: Systolic blood pressure in the aged group declined significantly from 155 ± 18 mmHg at baseline to 138 ± 11 mmHg after 12 weeks of treatment with azilsartan, and that in the non-aged group also declined significantly from 152 ± 20 mmHg at baseline to 142 ± 13 mmHg after 12 weeks of treatment with azilsartan. There were no significant differences in the magnitude of change in blood pressures from pre-treatment to post-treatment with azilsartan between the non-aged and aged groups. There were no changes in clinical laboratory findings, including serum levels of creatinine, potassium, lipids, and other metabolic variables, after 12 weeks of treatment with azilsartan in both groups. Conclusions: Our findings suggest that azilsartan is effective in lowering blood pressure in elderly patients and may be safe. Therefore, azilsartan could be a valuable option for treating hypertension in elderly and non-elderly patients.
Heart and Vessels | 2016
Manaka Tagaya; Daiji Yoshikawa; Yoshinori Sugishita; Fumi Yamauchi; Takehiro Ito; Tomohito Kamada; Masataka Yoshinaga; Daisuke Mukaide; Wakaya Fujiwara; Hiroatsu Yokoi; Mutsuharu Hayashi; Eiichi Watanabe; Junichi Ishii; Yukio Ozaki; Hideo Izawa
Journal of Cardiology | 2013
Daisuke Mukaide; Tomotsugu Tabata; Kosuke Kinoshita; Hiroatsu Yokoi; Wakaya Fujiwara; Osamu Inami; Yoshinori Sugishita; Gen Ukai; Masataka Yoshinaga; Tomohito Kamada; Masanori Nomura; Hideo Izawa
Journal of Cardiac Failure | 2017
Wakata Fujiwara; Ryo Yamada; Tomoya Ishiguro; Satoshi Okumura; Masataka Yoshinaga; Yoshinori Sugishita; Mutsuharu Hayashi; Yasuchika Kato; Yukio Ozaki; Hideo Izawa
Heart and Vessels | 2017
Mutsuharu Hayashi; Yoshinari Yasuda; Susumu Suzuki; Manaka Tagaya; Takehiro Ito; Tomohito Kamada; Masataka Yoshinaga; Yoshinori Sugishita; Wakaya Fujiwara; Hiroatsu Yokoi; Yukio Ozaki; Hideo Izawa
Journal of Cardiac Failure | 2016
Wakaya Fujiwara; Mutsuharu Hayashi; Yoshinori Sugishita; Masataka Yoshinaga; Tomoya Ishiguro; Hiroyuki Naruse; Junichi Ishii; Yasuchika Kato; Yukio Ozaki; Hideo Izawa
Internal Medicine | 2016
Mutsuharu Hayashi; Tomohito Kamada; Hiroatsu Yokoi; Wakaya Fujiwara; Daiji Yoshikawa; Daisuke Mukaide; Yoshinori Sugishita; Masataka Yoshinaga; Takehiro Ito; Yukio Ozaki; Hideo Izawa