研究者業績
基本情報
研究分野
1論文
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Annals of the American Thoracic Society 22(4) 609-611 2025年4月
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Sleep and biological rhythms 23(1) 29-37 2025年1月The purpose of this study was to evaluate how the first oral administration of suvorexant affects PSG results in patients with severe obstructive sleep apnea (OSA). Single-center, prospective study conducted in a nonrandomized, uncontrolled, unblinded fashion. Undiagnosed 64 patients with suspected OSA underwent first-night PSG, and 30 patients with severe OSA (Apnea Hypopnea Index [AHI] ≥ 30 events/h) underwent second-night PSG testing after administration of 15 mg suvorexant. The change in AHI between the first and second nights was not significant, although the upper limit of the 95% confidence interval for the mean difference in AHI was high at 5.987.The mean duration of apnea on the second night was significantly prolonged compared to that on the first night, but there were no significant differences n 3% oxygen desaturation index, saturation of percutaneous oxygen<90% time. On the second night, total sleep time was significantly prolonged, mid-night awakenings decreased, REM sleep percentage increased, and REM latency was shorter. Because the environment for PSG testing is very different from the patient's home and many patients have difficulty sleeping, there are clinical cases in which PSG is performed with sleep medication. In this study, PSG after oral administration of 15 mg of suvorexant on the second night showed no significant difference or clear trend in AHI. However, the upper limit of the 95% confidence interval for the mean difference in AHI was greater than 5, suggesting that suvorexant may exacerbate AHI, even with the first administration.
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BMC pulmonary medicine 24(1) 632-632 2024年12月26日BACKGROUND: The increasing prevalence of lung cancer in the elderly population necessitates a closer evaluation of diagnostic and therapeutic approaches. This study aimed to compare the safety and diagnostic efficacy of transbronchial lung cryobiopsy (TBLC) between patients ≥ 80 years and younger patients. METHODS: A retrospective review was conducted of 96 patients diagnosed with peripheral lung cancer who underwent TBLC between April 2021 and October 2023. The patients were categorized into two groups: the elderly group (age ≥ 80 years, n = 20) and younger group (age < 80 years; n = 76). Data regarding the biopsy yield, complications, and feasibility of molecular analyses were collected and analyzed. RESULTS: The diagnostic yield of TBLC was comparable between the elderly and younger groups (95% vs. 89.5%, p = 0.679). Biomarker testing, including programmed death-ligand 1 expression and genetic mutations, were feasible in all cases diagnosed with cancer using TBLC samples. No significant differences were observed in major complications such as pneumothorax or bleeding. CONCLUSIONS: TBLC was found to be a safe and effective diagnostic tool for peripheral lung cancer in elderly patients and provided adequate samples for molecular testing. Since the complication rates did not significantly differ between the two age groups, age alone should not be considered a contraindication for the procedure.
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Expert opinion on drug safety 2024年12月17日BACKGROUND: Immune checkpoint inhibitors (ICIs) play a central role in cancer immunotherapy. However, the occurrence of immune-related adverse events, especially ICI-induced interstitial lung disease (ICI-ILD), is life-threatening and affects the effectiveness of ICI treatment. This study aimed to explore potential drugs to mitigate ICI-ILD occurrence using data from the Japanese Adverse Drug Event Report (JADER) and the US Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS [JAPIC AERS]). RESEARCH DESIGN AND METHODS: We investigated concomitant drugs that reduce ILD associated with four ICIs - nivolumab, pembrolizumab, atezolizumab, and durvalumab - across the JADER and FAERS databases. Subsequently, the identified common concomitant drugs that reduce the occurrence of ICI-ILD were detected and analyzed. RESULTS: We found omega-3 fatty acids, loperamide, and amlodipine as common concomitant drugs that reduced ICI-ILD occurrence in both the JADER and FAERS databases. Omega-3 fatty acids reportedly have many effects in animal models of drug-induced ILD, including their association with ILD in humans and anti-inflammatory effects against ICI-ILD. However, loperamide and amlodipine reportedly have minimal effects against ILD, thereby necessitating further evaluation. CONCLUSION: Omega-3 fatty acids have emerged as potential agents for reducing ICI-ILD occurrence, as evidenced by findings from two different pharmacovigilance databases.
MISC
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BMC PULMONARY MEDICINE 14 14-14 2014年2月 査読有り
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GERIATRICS & GERONTOLOGY INTERNATIONAL 13(4) 986-992 2013年10月 査読有り
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Allergology international : official journal of the Japanese Society of Allergology 62(3) 367-73 2013年9月 査読有りBACKGROUND: Although a challenge test using non-steroidal anti-inflammatory drugs (NSAIDs) is crucial for diagnosis of aspirin-induced asthma (AIA), it also has drawbacks in terms of possible side effects. Therefore, alternative in-vitro diagnostic methods for AIA are awaited. METHODS: Nineteen stable non-AIA patients (9 males and 10 females; mean age, 49.4 ± 4.8 years), and 20 AIA patients (9 males and 11 females; mean age, 51.1 ± 4.8 years) were enrolled in this study. CD11b and CD16 expressions on the peripheral-blood granulocytes after administration of aspirin and different concentrations of PGE2 in vitro were examined using flowcytometry. RESULTS: Aspirin induced a significant increase in CD11b expression on eosinophils (CD16 negative granulocytes) in 19 AIA patients and one non-AIA patient. Increase in CD11b expression on eosinophils by aspirin administration was suppressed by PGE2 in a dose-dependent manner. CONCLUSIONS: The measurement of CD11b expression on peripheral-blood eosinophils showed very high sensitivity and specificity of (-95%) in diagnosing AIA. Although this method requires laboratory facilities for flowcytometry, it may be very useful in diagnosis of AIA without side effects. In addition, PGE2 may be involved in regulation of CD11b expression on eosinophils by aspirin administration.
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European journal of heart failure 15(9) 1003-10 2013年9月 査読有りAIMS: We examined whether the severity of central sleep apnoea (CSA) and the level of C-reactive protein are associated with the prevalence and complexity of arrhythmias, and whether these factors contribute to increased risk of nocturnal sudden death. METHODS AND RESULTS: We prospectively examined 178 patients (age 70 ± 1 years) who were admitted to our hospital due to worsening heart failure. We recorded a simultaneous overnight cardiorespiratory polygraph and Holter ECG. Obstructive sleep apnoea was excluded and patients were dichotomized based on the median value of the central apnoea index (CAI) of 7.5/h. The prevalence and complexity of arrhythmias were compared between daytime (06:00 h to 15:00 h) and night-time (21:00 h to 06:00 h). A multivariate logistic regression analysis revealed that the CAI was associated with prevalence of atrial fibrillation (AF) [odds ratio 1.03, 95% confidence interval (CI) 1.02-2.51)] and sinus pause during the night-time period (1.12, 95% CI 1.08-1.35). The CAI and C-reactive protein were independently associated with non-sustained ventricular tachycardia during both daytime (1.22, 95% CI 1.00-6.92; and 5.82, 2.58-56.1, respectively) and night-time periods (3.57, 95% CI 1.06-13.1; and 10.7, 3.30-44.4, respectively). During a mean follow-up period of 22 months, 30 (17%) patients had cardiovascular deaths and the CSA was an independent predictor (hazard ratio 1.29, 95% CI 1.16-2.32); only 5 (2.8%) of them died due to ventricular tachyarrhythmia, occurring during wakefulness. CONCLUSIONS: We demonstrated that the severity of CSA and C-reactive protein levels are independently associated with the prevalence and complexity of arrhythmias. CSA was associated with increased mortality risk, but it was not related directly to nocturnal death due to ventricular tachyarrhythmia.
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Respirology 18(2) 340-347 2013年2月 査読有り
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気管支学(日本呼吸器内視鏡学会雑誌) 35(2) 188-192 2013年 査読有り背景.骨転移を伴う悪性腫瘍を疑いEBUS-TBNAを施行した,縦隔副甲状腺嚢胞の1例を経験したので報告する.症例. 63歳男性.主訴は誤嚥,嗄声. PET-CTでFDGの集積を認める,上縦隔の嚢胞性病変および肋骨の溶骨性病変を認めた.縦隔病変に対しEBUS-TBNAを施行し,血性の液体成分を採取したが,悪性所見は認めなかった.肋骨病変に対する生検では副甲状腺機能亢進症に伴うbrown腫瘍の可能性が示され,血中副甲状腺ホルモン(intact PTH)は高値であった.縦隔副甲状腺嚢胞を摘出したところ骨病変は縮小した.結論.本症例は異所性副甲状腺嚢胞に肋骨brown腫瘍を伴ったものであり,稀な症例と考えられた.腫瘍性病変に高Ca血症を伴うことはしばしば見られるが,副甲状腺ホルモンの測定により異所性副甲状腺腫瘍を鑑別することが重要と考えられた.
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平成24年度 厚生労働科学研究費補助金 難治性疾患等克服研究事業 免疫アレルギー疾患等予防・治療研究事業 研究報告書(免疫アレルギー疾患分野) 288-292 2013年
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IMMUNOGENETICS 65(1) 17-24 2013年1月 査読有り
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INTERNAL MEDICINE 52(13) 1473-1478 2013年 査読有り
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Respiration; international review of thoracic diseases 86(3) 252-3 2013年 査読有り
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MOLECULAR CARCINOGENESIS 51(5) 400-410 2012年5月 査読有り
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INTERNATIONAL JOURNAL OF COMPUTER ASSISTED RADIOLOGY AND SURGERY 7(3) 359-369 2012年5月 査読有り
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平成23年度総括・分担研究報告書、厚生労働科学研究・免疫アレルギー疾患等予防・治療研究事業 23-26 2012年
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AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY 45(4) 684-691 2011年10月 査読有り
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ANTI-CANCER DRUGS 22(8) 811-816 2011年9月 査読有り
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NAGOYA JOURNAL OF MEDICAL SCIENCE 73(3-4) 69-78 2011年8月 査読有り
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Virtual bronchoscopy-guided transbronchial biopsy for aiding the diagnosis of peripheral lung cancerEUROPEAN JOURNAL OF RADIOLOGY 79(1) 155-159 2011年7月 査読有り
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Am J Respir Cell Mol Biol 44(5) 614-620 2011年 査読有り
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INTERNATIONAL JOURNAL OF CLINICAL ONCOLOGY 15(6) 583-587 2010年12月 査読有り
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CANCER SCIENCE 101(12) 2601-2605 2010年12月 査読有り
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AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY 43(2) 161-172 2010年8月 査読有り
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EUROPEAN JOURNAL OF PHARMACOLOGY 635(1-3) 204-211 2010年6月 査読有り
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AMERICAN JOURNAL OF THE MEDICAL SCIENCES 339(1) 41-48 2010年1月 査読有り
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INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY 30(10) 1019-1021 2009年10月 査読有り
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AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY 297(3) L420-L431 2009年9月 査読有り
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AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY 40(5) 536-542 2009年5月 査読有り
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Chest 135(3) 633-640 2009年3月 査読有り
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別冊日本臨床 新領域別症候群シリーズ 10 196-198 2009年
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肺癌 47(5) 491-491 2007年10月10日(一般演題(口演)9 癌性胸膜炎・心膜炎,第48回日本肺癌学会総会号)
書籍等出版物
2講演・口頭発表等
79共同研究・競争的資金等の研究課題
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日本学術振興会 科学研究費助成事業 2025年4月 - 2028年3月
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日本学術振興会 科学研究費助成事業 2023年4月 - 2026年3月
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日本学術振興会 科学研究費助成事業 2023年4月 - 2026年3月
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日本学術振興会 科学研究費助成事業 2022年4月 - 2025年3月
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日本学術振興会 科学研究費助成事業 2021年4月 - 2024年3月
その他教育活動上特記すべき事項
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件名第48回医学教育ワークショップ終了年月日2013/08/18概要「臨床実習学習成果の設定」に参加した。