Kazuki Nishida

Mr. Kazuki Nishida

Department of Biostatistics Section, Center for Advanced Medicine and Clinical Research, Nagoya University Graduate School of Medicine
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Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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4 June 2023 in Journal of Intensive Care Medicine
Verified
Journal Article
Closed access
DHDaisuke Hasegawa
Daisuke Hasegawa
YMYoshiko Mori
Yoshiko Mori
TMTetsuro Maeda
Tetsuro Maeda
NPNarut Prasitlumkum
Narut Prasitlumkum
KNKazuki Nishida
Kazuki Nishida
RSRyota Sato
Ryota Sato
Purpose: The prevalence and its impact on mortality of sepsis-induced cardiomyopathy (SICM) remain controversial. In this systematic review and meta-analysis, we investigated the prevalence and prognosis of SICM. Materials and Methods: We searched MEDLINE, Cochrane Central Register of Controlled Trials, and Embase. Titles and abstracts were evaluated based on the following criteria: (1) published in English, (2) randomized controlled trials, cohort studies, or cross-sectional studies, (3) ≥ 18 years with sepsis, (4) reporting the prevalence and/or comparison of short-term mortality between those with and without SICM, defined as the new-onset reduction in left ventricular ejection fraction (LVEF) within 72 h on admission or from the diagnosis of sepsis. The random-effect model was used for all analyses. This meta-analysis was registered at PROSPERO (CDR42022332896). Results: Sixteen studies reported the prevalence of SICM and the pooled prevalence of SICM was 20% (95% confidence interval [CI], 16-25%; I2 = 89.9%, P < 0.01). Eleven studies reported short-term mortality and SICM was associated with significantly higher short-term mortality (The pooled odds ratio: 2.30, 95% CI, 1.43-3.69; I2 = 0%, P = 0.001). Conclusion: The prevalence of SICM was 20% in patients with sepsis, and the occurrence of SICM was associated with significantly higher short-term mortality.

1 July 2019 in Resuscitation
Verified
Journal Article
Closed access
MNMitsuaki Nishikimi
Mitsuaki Nishikimi
TOTakayuki Ogura
Takayuki Ogura
KNKazuki Nishida
Kazuki Nishida
KTKunihiko Takahashi
Kunihiko Takahashi
MNMitsunobu Nakamura
Mitsunobu Nakamura
TITaku Iwami
Taku Iwami

1 March 2022 in Life Science Alliance
Verified
Journal Article
Open access
PDF file
YMYuki Miyai
Yuki Miyai
DSDaisuke Sugiyama
Daisuke Sugiyama
THTetsunari Hase
Tetsunari Hase
NANaoya Asai
Naoya Asai
TTTetsuro Taki
Tetsuro Taki
Atsushi EnomotoAtsushi Enomoto
Atsushi Enomoto
Cancer-associated fibroblasts (CAFs) are an integral component of the tumor microenvironment (TME). Most CAFs shape the TME toward an immunosuppressive milieu and attenuate the efficacy of immune checkpoint blockade (ICB) therapy. However, the detailed mechanism of how heterogeneous CAFs regulate tumor response to ICB therapy has not been defined. Here, we show that a recently defined CAF subset characterized by the expression of Meflin, a glycosylphosphatidylinositol-anchored protein marker of mesenchymal stromal/stem cells, is associated with survival and favorable therapeutic response to ICB monotherapy in patients with non-small cell lung cancer (NSCLC). The prevalence of Meflin-positive CAFs was positively correlated with CD4-positive T-cell infiltration and vascularization within non-small cell lung cancer tumors. Meflin deficiency and CAF-specific Meflin overexpression resulted in defective and enhanced ICB therapy responses in syngeneic tumors in mice, respectively. These findings suggest the presence of a CAF subset that promotes ICB therapy efficacy, which adds to our understanding of CAF functions and heterogeneity.

8 September 2021 in Critical Care Medicine
Verified
Journal Article
Closed access
RSRyota Sato
Ryota Sato
DHDaisuke Hasegawa
Daisuke Hasegawa
NPNarut Prasitlumkum
Narut Prasitlumkum
MUMiki Ueoka
Miki Ueoka
KNKazuki Nishida
Kazuki Nishida
SDSiddharth Dugar
Siddharth Dugar
OBJECTIVES: The aim of this study was to conduct a systematic review and meta-analysis of randomized controlled trials to investigate whether IV high-dose vitamin C improves the short-term mortality of patients with sepsis. DESIGN: This study is a systematic review and meta-analysis of randomized controlled trials. We searched EMBASE, the Cochrane Central Register of Controlled Trials, and MEDLINE for randomized controlled trials that met inclusion criteria. The protocol was registered at the University hospital Medical Information Network Clinical Trials Registry (UMIN000040528). All analyses were presented with the use of random-effects models. The primary outcome was short-term mortality defined as 28-day, 30-day, or in-hospital mortality. PATIENTS: Two authors independently evaluated the following eligibility criteria: 1) randomized controlled trial, 2) patients with sepsis aged ≥18 years, and 3) received intravenous high-dose vitamin C in addition to standard of care, or standard of care alone. Then, two authors independently extracted the selected patient and study characteristics and outcomes from studies that met above eligibility criteria. MEASUREMENTS AND MAIN RESULTS: Eleven randomized controlled trials (n = 1,737 patients) were included in this meta-analysis. High-dose IV vitamin C was not associated with a significantly lower short-term mortality (risk ratio, 0.88; 95% CI, 0.73–1.06; p = 0.18; I 2 = 29%) but was associated with a significantly shorter duration of vasopressor use (standardized mean difference, –0.35; 95% CI, –0.63 to –0.07; p < 0.01; I 2 = 80%) and a significantly greater decline in the Sequential Organ Failure Assessment score at 72–96 hours (standardized mean difference, –0.20; 95% CI, –0.32 to –0.08; p < 0.01; I 2 = 16%). One study reported significant association with hypernatremia, but adverse effects were rare, and high-dose vitamin C is deemed relatively safe. CONCLUSIONS: In this meta-analysis, the use of IV high-dose vitamin C in patients with sepsis was not associated with lower short-term mortality although it was associated with significantly shorter duration of vasopressor use and greater decline in the Sequential Organ Failure Assessment score at 72–96 hours.

1 June 2021 in Journal of Critical Care
Verified
Journal Article
Closed access
RSRyota Sato
Ryota Sato
DHDaisuke Hasegawa
Daisuke Hasegawa
NHNatsumi T. Hamahata
Natsumi T. Hamahata
SNSwetha Narala
Swetha Narala
KNKazuki Nishida
Kazuki Nishida
EDEhab G. Daoud
Ehab G. Daoud

27 November 2017 in Scientific Reports
Verified
Journal Article
Open access
PDF file
ASAkira Sayo
Akira Sayo
SUShinji Ueno
Shinji Ueno
TKTaro Kominami
Taro Kominami
KNKazuki Nishida
Kazuki Nishida
DIDaiki Inooka
Daiki Inooka
HTHiroko Terasaki
Hiroko Terasaki
The aim of this study is to determine the progress of the visual field defects obtained by the Humphrey Field Analyzer 10-2 program (HFA 10-2) in patients with retinitis pigmentosa (RP). The medical records of 45 eyes of 45 RP patients who had at least 3 visual field tests were reviewed. Linear mixed models were used to follow the changes of the mean deviation and the average sensitivity of 4, 12, and 20 points in three concentric squares, designated as S4, S12, and S20. The median follow-up time was 3.86 years [range: 1.93 to 9.86, IQR (Interquartile range): 3.01 to 4.93]. The median number of the visual field tests was 3 (range: 3 to 15, IQR: 3 to 4). The mean change of the MD was −0.46 dB/year (−5.80%/year). When the patients were grouped by the average initial MD, the less advanced group had slower progressions than the more advanced group in S4, S12, and S20. These results should be useful in understanding the pathological changes of RP in the central visual field.