Chisato Shimanoe
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Chisato Shimanoe has a total of 280 co-authors. Here are the top co-authors by number of shared publications:
- Isao Oze
Division of Cancer Information and Control Aichi Cancer Center Research Institute Nagoya Japan
19 shared publications - Yuichiro Nishida
Department of Preventive Medicine, Faculty of Medicine, Saga University, Saga, Japan
19 shared publications - Keitaro Matsuo
Division of Cancer Epidemiology and Prevention, Aichi Cancer Center Research Institute, Nagoya, Japan
18 shared publications - Sadao Suzuki
Department of Public Health, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan
18 shared publications - Megumi Hara
Department of Preventive Medicine, Faculty of Medicine, Saga University, 5-1-1 Nabeshima, Saga 849-8501, Japan
17 shared publications - Naoyuki Takashima
NCD Epidemiology Research Center, Shiga University of Medical Science, Otsu City, Shiga Prefecture, Japan (Drs Kita, Miura, and Takashima); Department of Epidemiology for Community Health and Medicine, Kyoto Prefectural University of Medicine, Kyoto City, Kyoto Prefecture, Japan (Dr Takashima)
17 shared publications
Latest Publications
- 3 September 2026
- Published by Elsevier in Journal of Infection and Chemotherapy
- Vol. 32 (11)
Relationship between albumin-bilirubin score and ceftriaxone-associated central nervous system toxicity: A matched case-control study
- 3 September 2026
- Published by Elsevier in Journal of Infection and Chemotherapy
- Vol. 32 (11)
Relationship between albumin-bilirubin score and ceftriaxone-associated central nervous system toxicity: A matched case-control study
- 18 August 2026
- Published by Wiley in Basic & Clinical Pharmacology & Toxicology
- Vol. 139 (3) , e70287
Discrepancies in Vancomycin Clearance Estimation Among Renal Function Models in Patients With Low Serum Creatinine Levels: A Pilot Study
Vancomycin dosing is guided by population pharmacokinetic models that consider renal function. However, low serum creatinine (Scr) levels may reflect heterogeneous conditions and lead to inaccurate vancomycin clearance. This study evaluated the predictive ability of different population pharmacokinetic models for vancomycin clearance in low Scr settings. This single‐centre retrospective study included hospitalised patients aged ≥18 years who received intravenous vancomycin. Predicted vancomycin clearance was calculated using population pharmacokinetic models across six scenarios incorporating creatinine clearance (Ccr), serum albumin, reduced muscle mass, Scr rounding and Japanese cystatin C–based estimated glomerular filtration rate (eGFR Japanese, Cys‐C ). Agreement was evaluated using concordance correlation coefficients (CCC) and Bland–Altman analysis. Among the six scenarios ( n = 24), the Ccr‐based model exhibited the best agreement (CCC = 0.79). Models based on eGFR Japanese, Cys‐C or rounded‐up Scr systematically underestimated clearance under augmented renal clearance. In those with a body mass index ≥25 kg/m 2 , clearance increased more substantially, and a similar trend was observed in patients aged <70 years. In patients with low Scr, Ccr‐based models showed better agreement with two‐point estimated vancomycin clearance. In obese or younger patients with low Scr, two‐point estimated vancomycin clearance may be a practical approach for vancomycin dosing.
- 18 August 2026
- Published by Wiley in Basic & Clinical Pharmacology & Toxicology
- Vol. 139 (3) , e70287
Discrepancies in Vancomycin Clearance Estimation Among Renal Function Models in Patients With Low Serum Creatinine Levels: A Pilot Study
Vancomycin dosing is guided by population pharmacokinetic models that consider renal function. However, low serum creatinine (Scr) levels may reflect heterogeneous conditions and lead to inaccurate vancomycin clearance. This study evaluated the predictive ability of different population pharmacokinetic models for vancomycin clearance in low Scr settings. This single‐centre retrospective study included hospitalised patients aged ≥18 years who received intravenous vancomycin. Predicted vancomycin clearance was calculated using population pharmacokinetic models across six scenarios incorporating creatinine clearance (Ccr), serum albumin, reduced muscle mass, Scr rounding and Japanese cystatin C–based estimated glomerular filtration rate (eGFR Japanese, Cys‐C ). Agreement was evaluated using concordance correlation coefficients (CCC) and Bland–Altman analysis. Among the six scenarios ( n = 24), the Ccr‐based model exhibited the best agreement (CCC = 0.79). Models based on eGFR Japanese, Cys‐C or rounded‐up Scr systematically underestimated clearance under augmented renal clearance. In those with a body mass index ≥25 kg/m 2 , clearance increased more substantially, and a similar trend was observed in patients aged <70 years. In patients with low Scr, Ccr‐based models showed better agreement with two‐point estimated vancomycin clearance. In obese or younger patients with low Scr, two‐point estimated vancomycin clearance may be a practical approach for vancomycin dosing.
- Open Access
- 16 March 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Data from The Significance of Comprehensive Metabolic Phenotypes in Cancer Risk: A Japan Multi-Institutional Collaborative Cohort Study
Supplementary File (List of the contributors to the J-MICC Study)
- 16 March 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Data from The Significance of Comprehensive Metabolic Phenotypes in Cancer Risk: A Japan Multi-Institutional Collaborative Cohort Study
Supplementary File (List of the contributors to the J-MICC Study)
- Open Access
- 27 September 2025
- Published by Elsevier in General Hospital Psychiatry
- Vol. 97, 72-78
Falls and fractures associated with ramelteon use: A systematic review and meta-analysis
- 27 September 2025
- Published by Elsevier in General Hospital Psychiatry
- Vol. 97, 72-78
Open AccessFalls and fractures associated with ramelteon use: A systematic review and meta-analysis
- 15 August 2025
- Published by Springer Nature in European Journal of Clinical Nutrition
- Vol. 79 (11) , 1106-1113
Dietary diversity and the risk of metabolic syndrome in a Japanese population: an analysis of baseline cross-sectional data from the J-MICC study
With the increasing burden of metabolic syndrome, it is crucial to focus on lifestyle factors to reduce the risk of metabolic syndrome. This study aims to quantify the associations between dietary diversity and the risk of metabolic syndrome among the Japanese population. This study was conducted using baseline data from the Japan Multi-Institutional Collaborative Cohort (J-MICC) study. The baseline survey was conducted from 2005 to 2014 by recruiting individuals aged 35-69. Information regarding dietary intake and biometric measurements were obtained. Dietary Diversity Score (DDS) was calculated from the data based on the food frequency questionnaire. A multiple logistic regression analysis was conducted to analyze the association between DDS and metabolic syndrome. In total, 75,332 participants were included for analysis. Inverse associations were observed between a high DDS and metabolic syndrome (adjusted odds ratio, 0.83 [95% confidential interval 0.76-0.92]). Likewise, a high DDS was associated with reduced odds of a high body mass index and hypertension. No significant associations were observed between the DDS and serum triglyceride, fasting blood glucose, or high-density lipoprotein cholesterol values. The findings of this study emphasize that dietary diversity has inversed associations with metabolic syndrome. Promoting a diverse and balanced diet can be a potential strategy for mitigating the burden of metabolic syndrome.
- 15 August 2025
- Published by Springer Nature in European Journal of Clinical Nutrition
- Vol. 79 (11) , 1106-1113
Dietary diversity and the risk of metabolic syndrome in a Japanese population: an analysis of baseline cross-sectional data from the J-MICC study
With the increasing burden of metabolic syndrome, it is crucial to focus on lifestyle factors to reduce the risk of metabolic syndrome. This study aims to quantify the associations between dietary diversity and the risk of metabolic syndrome among the Japanese population. This study was conducted using baseline data from the Japan Multi-Institutional Collaborative Cohort (J-MICC) study. The baseline survey was conducted from 2005 to 2014 by recruiting individuals aged 35-69. Information regarding dietary intake and biometric measurements were obtained. Dietary Diversity Score (DDS) was calculated from the data based on the food frequency questionnaire. A multiple logistic regression analysis was conducted to analyze the association between DDS and metabolic syndrome. In total, 75,332 participants were included for analysis. Inverse associations were observed between a high DDS and metabolic syndrome (adjusted odds ratio, 0.83 [95% confidential interval 0.76-0.92]). Likewise, a high DDS was associated with reduced odds of a high body mass index and hypertension. No significant associations were observed between the DDS and serum triglyceride, fasting blood glucose, or high-density lipoprotein cholesterol values. The findings of this study emphasize that dietary diversity has inversed associations with metabolic syndrome. Promoting a diverse and balanced diet can be a potential strategy for mitigating the burden of metabolic syndrome.
- 27 June 2025
- Published by Springer Nature in Hypertension Research
- Vol. 48 (9) , 2349-2357
Urinary cortisol-to-cortisone ratio levels modify the association between diabetes and hypertension: a cross-sectional study of 6931 older adults
The incidence of hypertension and Type 2 diabetes mellitus (T2DM) is increasing, and their coexistence significantly increases the risk of cardiovascular diseases, stroke, nephropathy, retinopathy, and mortality. Mineralocorticoid receptor activity, primarily regulated by aldosterone, can be beneficially modulated by mineralocorticoid receptor antagonists, especially in patients with mineralocorticoid receptor-associated hypertension, which often occurs with obesity and T2DM. Thus, markers of mineralocorticoid receptor activation, such as 11β-hydroxysteroid dehydrogenase, may help identify patients who may not benefit from standard hypertension treatments. This study investigated the effects of the cortisol-to-cortisone ratio, a marker of 11β-hydroxysteroid dehydrogenase activity, on the relationship between T2DM and hypertension. Using a cross-sectional design, 6931 individuals aged 45–74 years from the Japan Multi-Institutional Collaborative Cohort Study were analyzed. Cortisol and cortisone levels in spot urine samples were measured using liquid chromatography-mass spectrometry. Hypertension (N = 3141) was observed among those who were older; male; current smokers; current drinkers; had T2DM, hyperlipidemia, high BMI; and low perceived stress, physical activity, and eGFR. Multiple logistic regression analysis was performed, and T2DM was associated with hypertension (odds ratio, 1.37; 95% CI, 1.14–1.66). This association varied with cortisol-to-cortisone ratio level and was more evident in participants with a higher odds ratio (2.01; 95% CI, 1.39–2.91; Pinteraction = 0.040). These epidemiologic findings suggest that mineralocorticoid receptor activity and 11β-hydroxysteroid dehydrogenase regulation may play a role in hypertension among patients with T2DM, highlighting the potential for targeted treatments based on the cortisol-to-cortisone ratio.
- 27 June 2025
- Published by Springer Nature in Hypertension Research
- Vol. 48 (9) , 2349-2357
Urinary cortisol-to-cortisone ratio levels modify the association between diabetes and hypertension: a cross-sectional study of 6931 older adults
The incidence of hypertension and Type 2 diabetes mellitus (T2DM) is increasing, and their coexistence significantly increases the risk of cardiovascular diseases, stroke, nephropathy, retinopathy, and mortality. Mineralocorticoid receptor activity, primarily regulated by aldosterone, can be beneficially modulated by mineralocorticoid receptor antagonists, especially in patients with mineralocorticoid receptor-associated hypertension, which often occurs with obesity and T2DM. Thus, markers of mineralocorticoid receptor activation, such as 11β-hydroxysteroid dehydrogenase, may help identify patients who may not benefit from standard hypertension treatments. This study investigated the effects of the cortisol-to-cortisone ratio, a marker of 11β-hydroxysteroid dehydrogenase activity, on the relationship between T2DM and hypertension. Using a cross-sectional design, 6931 individuals aged 45–74 years from the Japan Multi-Institutional Collaborative Cohort Study were analyzed. Cortisol and cortisone levels in spot urine samples were measured using liquid chromatography-mass spectrometry. Hypertension (N = 3141) was observed among those who were older; male; current smokers; current drinkers; had T2DM, hyperlipidemia, high BMI; and low perceived stress, physical activity, and eGFR. Multiple logistic regression analysis was performed, and T2DM was associated with hypertension (odds ratio, 1.37; 95% CI, 1.14–1.66). This association varied with cortisol-to-cortisone ratio level and was more evident in participants with a higher odds ratio (2.01; 95% CI, 1.39–2.91; Pinteraction = 0.040). These epidemiologic findings suggest that mineralocorticoid receptor activity and 11β-hydroxysteroid dehydrogenase regulation may play a role in hypertension among patients with T2DM, highlighting the potential for targeted treatments based on the cortisol-to-cortisone ratio.
- Open Access
- 3 April 2025
- Published by American Association for Cancer Research (AACR)
Supplementary Data from The Significance of Comprehensive Metabolic Phenotypes in Cancer Risk: A Japan Multi-Institutional Collaborative Cohort Study
Supplementary File (List of the contributors to the J-MICC Study)
- 3 April 2025
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Data from The Significance of Comprehensive Metabolic Phenotypes in Cancer Risk: A Japan Multi-Institutional Collaborative Cohort Study
Supplementary File (List of the contributors to the J-MICC Study)