1.Sarcopenia as a Robust Predictor of Readmission within 6 Months among Individuals Experiencing Acute Stroke
Takafumi ABE ; Yoshihiro YOSHIMURA ; Yoichi SATO ; Fumihiko NAGANO ; Ayaka MATSUMOTO
Annals of Geriatric Medicine and Research 2024;28(3):307-314
		                        		
		                        			 Background:
		                        			Sarcopenia negatively affects the short-term prognosis of hospitalized older adults. However, no evidence currently supports a direct relationship between sarcopenia and readmission among individuals who have experienced an acute stroke. Therefore, we investigated whether sarcopenia is associated with readmission after discharge. 
		                        		
		                        			Methods:
		                        			This retrospective cohort study included patients who had experienced acute stroke. Sarcopenia was defined as the coexistence of low skeletal muscle mass index (SMI) and grip strength. We applied the log-rank test and Cox proportional hazards regression analysis to analyze whether sarcopenia, low SMI, and low grip strength were associated with readmission within 6 months. 
		                        		
		                        			Results:
		                        			Among 228 included patients (mean age, 72.8 years; 146 males), the prevalence of sarcopenia was 24.6% (n=56; male 17.8%; female 36.6%). Cox proportional hazards regression analysis using the propensity score as a covariate revealed that sarcopenia (hazard ratio [HR]=7.21; 95% confidence interval [CI] 1.45–35.8; p=0.016) and low skeletal muscle mass (HR=7.40; 95% CI 1.14–48.1; p=0.036), but not low grip strength (HR=1.42; 95% CI 0.281–7.21; p=0.670), were significantly associated with readmission for stroke within 6 months. 
		                        		
		                        			Conclusions
		                        			Sarcopenia was negatively associated with readmission within 6 months of stroke onset in patients in Japan who had experienced an acute stroke. These findings suggest that the identification of sarcopenia may facilitate prognostic prediction from the acute stage and intervention(s) to prevent rehospitalization. 
		                        		
		                        		
		                        		
		                        	
2.Development of Nursing Practice Scale of Cancer Pain Management and Examination of Reliability and Validity
Noriko TAKAHASHI ; Maho AOYAMA ; Kazuki SATO ; Yoichi SHIMIZU ; Naoko IGARASHI ; Mitsunori MIYASHITA
Palliative Care Research 2023;18(1):19-29
		                        		
		                        			
		                        			The aims of this study were (1) to develop and validate the scale to measure evidence-based nursing practice in cancer pain management and (2) to identify associated factors. We developed potential items based on the 2014 version of Japanese Clinical Guidelines for Cancer Pain Management and administered anonymous questionnaire for 189 oncology nurses in a designated cancer center. We conducted a re-test to test reliability.167 nurses participated in the study. As a result of item analysis and exploratory factor analysis, we developed a nursing practice scale of cancer pain management and its shortened version. This scale consists of 1 domain 50 items The Cronbach’s α coefficient showing internal consistency was 0.98 (shortened version 0.88). The intra-class correlation coefficient of reliability was 0.52 (shortened version 0.77). Concurrent validity was confirmed by the correlation between the total score of the whole scale and the total score of the practice of palliative care, knowledge, difficulty, self-confidence scale. We concluded that this scale was valid and reliable. Factors related to the nursing practice of cancer pain management were years of experience in cancer nursing, opportunities of postgraduate education, and satisfaction with postgraduate education. This scale can be used for evaluation of daily clinical practice and practice evaluation after educational efforts such as cancer pain nursing training.
		                        		
		                        		
		                        		
		                        	
3.Analysis of bone in adenine-induced chronic kidney disease model rats
Hikaru SAITO ; Naohisa MIYAKOSHI ; Yuji KASUKAWA ; Koji NOZAKA ; Hiroyuki TSUCHIE ; Chiaki SATO ; Kazunobu ABE ; Ryo SHOJI ; Yoichi SHIMADA
Osteoporosis and Sarcopenia 2021;7(4):121-126
		                        		
		                        			 Objectives:
		                        			The purpose of this study is to investigate the stage of chronic kidney disease (CKD) in adenine-induced CKD model rats by serum analyses, and to examine bone mineral density (BMD), bone strength, and microstructure of trabecular and cortical bone in these rats. 
		                        		
		                        			Methods:
		                        			Eight-week-old, male Wistar rats (n = 42) were divided into 2 groups: those fed a 0.75% adenine diet for 4 weeks until 12 weeks of age to generate CKD model rats (CKD group); and sham rats. The CKD and sham groups were sacrificed at 12, 16, and 20 weeks of age (n = 7 in each group and at 12, 16, and 20 weeks), and various parameters were evaluated, including body weight, renal wet weight, muscle wet weight, renal histology, biochemical tests, BMD, biomechanical testing, and micro-computed tomography (CT). The parameters were compared between the 2 groups at the various time points. 
		                        		
		                        			Results:
		                        			In the CKD model rats, at 20 weeks of age, serum creatinine, phosphorus, and intact-PTH levels were elevated, and serum calcium levels were normal, indicating that the CKD was stage IV and associated with secondary hyperparathyroidism. Decreased BMDs of the whole body and the femur were observed as bone changes, and micro-CT analysis showed deterioration of bone microstructure of the cortical bone that resulted in decreased bone strength in the cortical and trabecular bone. 
		                        		
		                        			Conclusions
		                        			These CKD model rats showed stage IV CKD and appear appropriate for evaluating the effects of several treatments for CKD-related osteoporosis and mineral bone disorder. 
		                        		
		                        		
		                        		
		                        	
4.Effects of teriparatide on bone in autochthonous transgenic model mice for diabetes mellitus (Akita mice)
Kentaro OHUCHI ; Naohisa MIYAKOSHI ; Yuji KASUKAWA ; Toyohito SEGAWA ; Hayato KINOSHITA ; Chie SATO ; Masashi FUJII ; Yoichi SHIMADA
Osteoporosis and Sarcopenia 2019;5(4):109-115
		                        		
		                        			 OBJECTIVES:
		                        			The purpose of this study is to evaluate the effects of teriparatide (TPTD) on bone mineral density (BMD), bone strength, and bone quality in Akita mouse models of diabetes mellitus.
		                        		
		                        			METHODS:
		                        			Twelve-week-old female Akita mice and control mice (C57/BL/6NCrSlc) were divided into 4 groups: control mice treated with vehicle (n = 7) or TPTD (n = 6); and Akita mice treated with vehicle (n = 6) or TPTD (n = 7). TPTD or vehicle was administered subcutaneously 3 times a week for 8 weeks. Blood glucose, serum sclerostin, total tibial BMD, femoral shaft bone strength, and bone quality using Fourier-transform infrared spectroscopy imaging were evaluated.
		                        		
		                        			RESULTS:
		                        			No significant differences in serum sclerostin levels were evident among these groups after 8 weeks of treatment. TPTD significantly increased BMD in control mice (+12.7%, P = 0.02) and Akita mice (+29.2%, P = 0.001) compared with vehicle. Maximum load and stiffness were significantly higher in Akita mice treated with TPTD than in Akita mice treated with vehicle (+56.6%, P = 0.03 and + 90.5%, P = 0.02, respectively). On Fourier-transform infrared spectroscopy imaging, the mineral/matrix ratio was significantly lower in Akita mice treated with vehicle than in control mice (−12.2%, P = 0.02), and TPTD treatment significantly increased the mineral/matrix ratio (P = 0.003).
		                        		
		                        			CONCLUSIONS
		                        			TPTD thus improved BMD and bone strength in both control mice and Akita mice, with improvements in the mineral/matrix ratio among Akita mice. 
		                        		
		                        		
		                        		
		                        	
5.Surgical Results of Patients with Myelopathy due to Ossification of the Ligamentum Flavum with Ossification of the Posterior Longitudinal Ligament or a Vertebral Fracture at the Same Level of the Thoracic Spine: A Retrospective Comparative Study
Yuji KASUKAWA ; Naohisa MIYAKOSHI ; Michio HONGO ; Yoshinori ISHIKAWA ; Daisuke KUDO ; Ryota KIMURA ; Yuichi ONO ; Jumpei IIDA ; Chiaki SATO ; Yoichi SHIMADA
Asian Spine Journal 2019;13(5):832-841
		                        		
		                        			
		                        			STUDY DESIGN: Retrospective and comparative study. PURPOSE: We assessed surgical treatment outcomes in patients with thoracic myelopathy due to ossification of the ligamentum flavum (OLF), and OLF combined with ossification of the posterior longitudinal ligament (OPLL) or vertebral fracture (VF) at the same level. OVERVIEW OF LITERATURE: OLF and OPLL cause severe thoracic myelopathy. Osteoporotic VF commonly occurs at the thoracolumbar junction. There have been no investigations of thoracic myelopathy due to OLF and VF. METHODS: Forty patients were divided among three groups: the OLF group (n=23): myelopathy due to OLF, the OLF+OPLL group (n=12): myelopathy due to OLF and OPLL, and the OLF+VF group (n=5): myelopathy due to OLF and VF. We recorded OLF, OPLL, and VF sites and operative procedures. Each patient’s neurological status, according to the Japanese Orthopaedic Association (JOA) score, and walking ability were evaluated pre- and postoperatively. RESULTS: Patients in the OLF+OPLL group were significantly younger than those in the other two groups. The preoperative JOA score was significantly lower in the OLF+VF than OLF group. The final JOA score was significantly lower in the OLF+VF than OLF and OLF+OPLL groups. The JOA score recovery rate was significantly lower in the OLF+VF than OLF group. Final walking ability was significantly worse in the OLF+OPLL and OLF+VF groups than in the OLF group and significantly worse in the OLF+VF than OLF+OPLL group. CONCLUSIONS: Thoracic myelopathy due to OLF+VF occurs primarily in older females, who also exhibit worse preoperative and postoperative neurological status, and worse walking ability, than patients with thoracic myelopathy due to OLF or OLF+OPLL.
		                        		
		                        		
		                        		
		                        	
6.The use of conization to identify and treat severe lesions among prediagnosed CIN1 and 2 patients in Japan.
Mikio MIKAMI ; Masae IKEDA ; Hidetaka SATO ; Haruko IWASE ; Takayuki ENOMOTO ; Yoichi KOBAYASHI ; Hidetaka KATABUCHI
Journal of Gynecologic Oncology 2018;29(4):e46-
		                        		
		                        			
		                        			OBJECTIVE: To evaluate the clinical efficiency of identifying patients with suspicious severe lesions by conization among prediagnosed cervical intraepithelial neoplasia (CIN) 1 and 2 patients in Japan. METHODS: The data in a Japanese nation-wide registry for cervical cancer (2009 and 2011) was collected to analyze the clinical efficacy of pre- and postdiagnosis for 13,215 Japanese women who underwent treatment by conization. Their preoperative and postoperative histologic findings and clinical outcomes were evaluated using standard statistical procedures including clinical and demographic characteristics. RESULTS: Almost half of 1,536 women who were treated by conization after the prediagnosis of CIN1 and 2 because the lesions showed no evidence of natural regression actually contained CIN1–2 (45.0%), CIN3 (47%), or invasive cancer (2.7%) in their cervical tissue. They underwent conization either for therapeutic (treatment) (78.5%) or diagnostic (21.5%) reasons. Invasive disease was diagnosed postoperatively more often in diagnostic cases (6.1%) than in therapeutic cases (2.8%). All the patients survived their diagnostic and therapeutic conization after approximately 30 months of follow up. CONCLUSION: Our study shows that the continuous observation of the prediagnosed CIN1 and 2 cases by the combination of cytology, colposcopy and histology in Japan has worked successfully to identify severe lesions by using conization as well in the process.
		                        		
		                        		
		                        		
		                        			Asian Continental Ancestry Group
		                        			;
		                        		
		                        			Cervical Intraepithelial Neoplasia
		                        			;
		                        		
		                        			Colposcopy
		                        			;
		                        		
		                        			Conization*
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Follow-Up Studies
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Japan*
		                        			;
		                        		
		                        			Treatment Outcome
		                        			;
		                        		
		                        			Uterine Cervical Neoplasms
		                        			
		                        		
		                        	
7.Effects of eldecalcitol and ibandronate on secondary osteoporosis and muscle wasting in rats with adjuvant-induced arthritis
Yuichi ONO ; Naohisa MIYAKOSHI ; Yuji KASUKAWA ; Hiroyuki NAGASAWA ; Hiroyuki TSUCHIE ; Manabu AKAGAWA ; Itsuki NAGAHATA ; Yusuke YUASA ; Chiaki SATO ; Yoichi SHIMADA
Osteoporosis and Sarcopenia 2018;4(4):128-133
		                        		
		                        			
		                        			OBJECTIVES: Rheumatoid arthritis (RA) is characterized by chronic inflammation of the synovium, progressive erosion of the articular cartilage, and joint destruction. RA also causes secondary osteoporosis and muscle wasting. We investigated the effects of ibandronate (IBN), a bisphosphonate; eldecalcitol (ELD), an active vitamin D3 derivative; and combination treatment with both agents on secondary osteoporosis and muscle wasting using adjuvant-induced arthritis rats. METHODS: Arthritis was induced in 8-week-old male Lewis rats. Rats were randomized into 4 treatment groups and an untreated normal control group: IBN (subcutaneously, once every 2 weeks, 10 µg/kg), ELD (orally, once daily, 30 ng/kg/day), IBN + ELD, vehicle, and control. Paw thickness measurements were performed for evaluation of arthritis. The femur was scanned using dual-energy X-ray absorptiometry. Cross-sectional areas of left tibialis and anterior muscle fibers and the expression of MuRF1, atrogin-1, MyoD, and myogenin in the gastrocnemius muscle were measured to evaluate muscle wasting. RESULTS: IBN and/or ELD increased bone mineral density (BMD) in the femur. In addition, there was an additive effect of combination treatment compared with single treatments for BMD. However, IBN and/or ELD did not inhibit muscle wasting in adjuvant-induced arthritis rats. CONCLUSIONS: Combination treatment with IBN and ELD may be effective for secondary osteoporosis associated with RA. Other treatments are necessary for muscle wasting associated with RA. Studies in humans are needed to confirm these findings.
		                        		
		                        		
		                        		
		                        			Absorptiometry, Photon
		                        			;
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Arthritis
		                        			;
		                        		
		                        			Arthritis, Rheumatoid
		                        			;
		                        		
		                        			Bone Density
		                        			;
		                        		
		                        			Cartilage, Articular
		                        			;
		                        		
		                        			Cholecalciferol
		                        			;
		                        		
		                        			Femur
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Inflammation
		                        			;
		                        		
		                        			Joints
		                        			;
		                        		
		                        			Male
		                        			;
		                        		
		                        			Muscle, Skeletal
		                        			;
		                        		
		                        			Myogenin
		                        			;
		                        		
		                        			Osteoporosis
		                        			;
		                        		
		                        			Rats
		                        			;
		                        		
		                        			Synovial Membrane
		                        			;
		                        		
		                        			Vitamin D
		                        			
		                        		
		                        	
8.Short-Term Results of Hybrid Closed-Wedge High Tibial Osteotomy: A Case Series with a Minimum 3-Year Follow-up
Hidetomo SAITO ; Kimio SAITO ; Yoichi SHIMADA ; Toshiaki YAMAMURA ; Shin YAMADA ; Takahiro SATO ; Koji NOZAKA ; Hiroaki KIJIMA ; Naohisa MIYAKOSHI
The Journal of Korean Knee Society 2018;30(4):293-302
		                        		
		                        			
		                        			PURPOSE: High tibial valgus osteotomy (HTO) is a well-established surgical procedure for patients with medial compartment osteoarthritis (OA) of the knee. The hybrid closed-wedge HTO (CWHTO) procedure permits extensive correction in patients with severe deformities or patellofemoral joint OA. The aim of this study was to report the short-term results in a consecutive series of patients treated with hybrid CWHTO. MATERIALS AND METHODS: We retrospectively evaluated the clinical outcomes and radiographic parameters in 29 consecutive knees that underwent hybrid CWTHO to correct medial compartment OA at an average follow-up of 52.6 months. Clinical outcomes were assessed using the Lysholm score and knee scoring system of the Japanese Orthopedic Association (JOA). The Kellgren-Lawrence grading system and pre- and postoperative mechanical axis (MA), femorotibial angle (FTA), posterior tibial slope, and patella height were assessed. RESULTS: The FTA and MA significantly changed from 180.7° to 170.4° and from 22.0° to 60.2°, respectively. No significant differences were observed between the mean pre- and postoperative posterior tibial slope, Insall-Salvati ratio, or Caton-Deschamps index. The postoperative JOA and Lysholm scores significantly improved from 76.7 to 95.8 and from 58.8 to 90.2, respectively. CONCLUSIONS: Satisfactory outcomes can be achieved with hybrid CWHTO in patients with medial OA.
		                        		
		                        		
		                        		
		                        			Asian Continental Ancestry Group
		                        			;
		                        		
		                        			Congenital Abnormalities
		                        			;
		                        		
		                        			Follow-Up Studies
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Knee
		                        			;
		                        		
		                        			Orthopedics
		                        			;
		                        		
		                        			Osteoarthritis
		                        			;
		                        		
		                        			Osteotomy
		                        			;
		                        		
		                        			Patella
		                        			;
		                        		
		                        			Patellofemoral Joint
		                        			;
		                        		
		                        			Retrospective Studies
		                        			
		                        		
		                        	
9.NUDT15, FTO, and RUNX1 genetic variants and thiopurine intolerance among Japanese patients with inflammatory bowel diseases.
Toshiyuki SATO ; Tetsuya TAKAGAWA ; Yoichi KAKUTA ; Akihiro NISHIO ; Mikio KAWAI ; Koji KAMIKOZURU ; Yoko YOKOYAMA ; Yuko KITA ; Takako MIYAZAKI ; Masaki IIMURO ; Nobuyuki HIDA ; Kazutoshi HORI ; Hiroki IKEUCHI ; Shiro NAKAMURA
Intestinal Research 2017;15(3):328-337
		                        		
		                        			
		                        			BACKGROUND/AIMS: Recent genome-wide analyses have provided strong evidence concerning adverse events caused by thiopurine drugs such as azathioprine (AZA) and 6-mercaptopurine. The strong associations identified between NUDT15 p.Arg139Cys and thiopurine-induced leukopenia and severe hair loss have been studied and confirmed over the last 2 years. However, other coding variants, including NUDT15 p.Val18_Val19insGlyVal, NUDT15 p.Val18Ile, and FTO p.Ala134Thr, and a noncoding variation in RUNX1 (rs2834826) remain to be examined in detail in this respect. Therefore, we investigated the correlation between these adverse events and the 5 recently identified variants mentioned above among Japanese patients with inflammatory bowel diseases (IBD). METHODS: One hundred sixty thiopurine-treated patients with IBD were enrolled. Genotyping was performed using TaqMan SNP Genotyping Assays or Sanger sequencing. RESULTS: None of the 5 variants were associated with gastrointestinal intolerance to AZA. However, NUDT15 p.Arg139Cys was significantly associated with the interval between initiation and discontinuation of AZA among patients with gastrointestinal intolerance. This variant was strongly associated with early (<8 weeks) and late (≥8 weeks) leukopenia and severe hair loss. Moreover, it correlated with the interval between initiation of thiopurine therapy and leukopenia occurrence, and average thiopurine dose. NUDT15 p.Val18_Val19insGlyVal, NUDT15 p.Val18Ile, FTO p.Ala134Thr, and RUNX1 rs2834826 exhibited no significant relationship with the adverse events examined. CONCLUSIONS: Of the 5 variants investigated, NUDT15 p.Arg139Cys had the strongest impact on thiopurine-induced leukopenia and severe hair loss; therefore, its genotyping should be prioritized over that of other variants in efforts to predict these adverse events in Japanese patients with IBD.
		                        		
		                        		
		                        		
		                        			6-Mercaptopurine
		                        			;
		                        		
		                        			Asian Continental Ancestry Group*
		                        			;
		                        		
		                        			Azathioprine
		                        			;
		                        		
		                        			Clinical Coding
		                        			;
		                        		
		                        			Hair
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Inflammatory Bowel Diseases*
		                        			;
		                        		
		                        			Leukopenia
		                        			
		                        		
		                        	
10.Effects of combined therapy of alendronate and low-intensity pulsed ultrasound on metaphyseal bone repair after osteotomy in the proximal tibia of glucocorticoid-induced osteopenia rats.
Tetsuya KAWANO ; Naohisa MIYAKOSHI ; Yuji KASUKAWA ; Michio HONGO ; Hiroyuki TSUCHIE ; Chie SATO ; Masashi FUJII ; Masazumi SUZUKI ; Manabu AKAGAWA ; Yuichi ONO ; Yusuke YUASA ; Itsuki NAGAHATA ; Yoichi SHIMADA
Osteoporosis and Sarcopenia 2017;3(4):185-191
		                        		
		                        			
		                        			OBJECTIVES: Glucocorticoid (GC) treatment inhibits activation of runt-related transcription factor 2 (Runx2), which is essential for osteoblast differentiation from stem cells. As a result, GC treatment results in bone loss, GC-induced osteoporosis (GIO), elevated fracture risk, and delayed bone healing. Bisphosphonates such as alendronate (ALN) are recommended for treating or preventing GIO, and lowintensity pulsed ultrasound (LIPUS) facilitates fracture healing and maturation of regenerated bone. Combined therapy with ALN and LIPUS may stimulate cancellous bone healing in GIO rats. Here, we examined the effect of ALN and LIPUS on cancellous bone osteotomy repair in the proximal tibia of GIO rats. METHODS: Prednisolone (10 mg/kg body weight/day) was administered for 4 weeks to induce GIO in 6-month-old female Sprague-Dawley rats. Tibial osteotomy was then performed and daily subcutaneous injection of ALN (1-µg/kg body weight) was subsequently administered alone or in combination with LIPUS (20 min/day) for 2 or 4 weeks. RESULTS: ALN significantly increased bone mineral density (BMD) at 2 and 4 weeks, and ALN + LIPUS significantly increased BMD at 4 weeks. Bone union rates were significantly increased after 2 and 4 weeks ALN and ALN + LIPUS treatment. Lastly, ALN and ALN + LIPUS significantly increased the proportion of Runx2 positive cells at 4 weeks. CONCLUSIONS: ALN monotherapy and combined ALN and LUPUS treatment augmented BMD and stimulated cancellous bone repair with increased Runx2 expression at the osteotomy site in GIO rats. However, the combined treatment had no additional effect on cancellous bone healing compared to ALN monotherapy.
		                        		
		                        		
		                        		
		                        			Alendronate*
		                        			;
		                        		
		                        			Animals
		                        			;
		                        		
		                        			Bone Density
		                        			;
		                        		
		                        			Bone Diseases, Metabolic*
		                        			;
		                        		
		                        			Diphosphonates
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Fracture Healing
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Infant
		                        			;
		                        		
		                        			Injections, Subcutaneous
		                        			;
		                        		
		                        			Osteoblasts
		                        			;
		                        		
		                        			Osteoporosis
		                        			;
		                        		
		                        			Osteotomy*
		                        			;
		                        		
		                        			Prednisolone
		                        			;
		                        		
		                        			Rats*
		                        			;
		                        		
		                        			Rats, Sprague-Dawley
		                        			;
		                        		
		                        			Stem Cells
		                        			;
		                        		
		                        			Tibia*
		                        			;
		                        		
		                        			Transcription Factors
		                        			;
		                        		
		                        			Ultrasonic Waves*
		                        			
		                        		
		                        	
            

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