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1.
J Oral Rehabil ; 43(5): 333-9, 2016 May.
Article in English | MEDLINE | ID: mdl-26946239

ABSTRACT

The aim of this study was to investigate the bone resorption effect of the mediators delivered in joint cavity of patients with mandibular condyle fractures by detecting osteoclast markers using cellular biochemistry methods, and by analysing bone resorption activities via inducing osteoclast differentiation of the infiltrated cells from arthrocentesis. Sixteen joints in 10 patients with mandibular condyle fractures were evaluated. The control group consisted of synovial fluid (SF) samples from seven joints of four volunteers who had no clinical signs or symptoms involving the temporomandibular joint (TMJ) or disc displacement. We collected SF cells from all patients during therapeutic arthrocentesis. The infiltrating cells from TMJ SF were cultured, differentiated into tartrate-resistant acid phosphatase (TRAP)-positive osteoclast-like cells and examined bone resorption activities. We also investigated factors related to osteoclast induction of SF, using ELISA procedures. Osteoclast-like cells were induced from the SF cells obtained from all patients with condylar fractures. These multinucleated giant cells were positive for TRAP and actin, and had the ability to absorb dentin slices. The levels of macrophage colony-stimulating factor (M-CSF), prostaglandin E2 (PGE2), soluble form of receptor activator of nuclear factor kappa-B ligand (sRANKL) and osteoprotegerin (OPG), in SF samples from the patients, were significantly higher than in the controls. These findings indicate that bone resorption activities in SF from patients with mandibular condyle fractures were upregulated and may participate in the pathogenesis and wound healing.


Subject(s)
Bone Resorption/pathology , Mandibular Condyle/pathology , Mandibular Fractures/pathology , Osteoclasts/metabolism , Synovial Fluid/cytology , Temporomandibular Joint/pathology , Adolescent , Adult , Biomarkers/metabolism , Cell Differentiation , Cells, Cultured , Child , Cytokines , Female , Humans , Male , Mandibular Condyle/injuries , Mandibular Fractures/metabolism , Middle Aged , Osteoprotegerin/metabolism , RANK Ligand/metabolism , Temporomandibular Joint/metabolism , Young Adult
2.
Diabet Med ; 32(9): 1221-6, 2015 Sep.
Article in English | MEDLINE | ID: mdl-25683576

ABSTRACT

AIMS: A close association between heart rate-corrected QT interval (QTc) and albuminuria in people with Type 2 diabetes has been reported in cross sectional studies. The aim of this study was to evaluate the relationship between QTc and change in urine albumin excretion (UAE) or progression of albuminuria in people with Type 2 diabetes. METHODS: We measured QTc in 251 consecutive people at baseline. We performed a 5-year follow-up cohort study to assess the relationship between QTc and change in UAE, defined as an increase of UAE/follow-up duration (year), or progression of albuminuria, defined as an increase in the category of diabetic nephropathy. RESULTS: During follow-up, 23 of 151 people with normoalbuminuria and 13 of 73 people with microalbuminuria at baseline had progression of albuminuria. Multiple regression analysis demonstrated that QTc was independently associated with change in UAE (ß = 0.176, P = 0.0104). Logistic regression analyses showed that QTc was a risk marker for progression of albuminuria [odds ratio per 0.01-s increase in QTc 1.35, 95% confidence interval (CI) 1.11-1.66, P = 0.0024] after adjusting for confounders. According to the receiver operator characteristic (ROC) analysis, the optimal cut-off point of QTc for progression of albuminuria was 0.418 s [area under the ROC curve 0.75 (95% CI 0.66-0.82), sensitivity = 0.86, specificity = 0.56, P < 0.0001]. CONCLUSIONS: Heart rate-corrected QT interval could be a novel risk marker for progression of albuminuria in people with Type 2 diabetes.


Subject(s)
Albuminuria/diagnosis , Diabetes Mellitus, Type 2/diagnosis , Diabetic Nephropathies/diagnosis , Heart Rate/physiology , Aged , Albuminuria/physiopathology , Biomarkers/urine , Diabetes Mellitus, Type 2/physiopathology , Diabetes Mellitus, Type 2/urine , Diabetic Nephropathies/physiopathology , Diabetic Nephropathies/urine , Disease Progression , Electrocardiography , Female , Humans , Male , ROC Curve , Retrospective Studies , Risk Factors
3.
Br J Surg ; 101(3): 232-8, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24402763

ABSTRACT

BACKGROUND: The aim of this study was to evaluate the use of intestinal fatty acid binding protein (I-FABP) and traditional biomarkers in the early diagnosis of acute intestinal ischaemia of different causes. METHODS: I-FABP, white blood cell (WBC) count, C-reactive protein, base deficit, lactate, lactate dehydrogenase, aspartate aminotransferase, creatine kinase and D-dimer were measured prospectively in consecutive patients suspected of having acute intestinal ischaemia. Biomarker levels were compared in patients with vascular and non-vascular ischaemia. RESULTS: Two hundred and eight patients with a clinical suspicion of acute intestinal ischaemia were enrolled. Vascular intestinal ischaemia was diagnosed in 24 patients (11·5 per cent), non-vascular ischaemia in 62 (29·8 per cent) and non-ischaemic disease in 122 (58·7 per cent). The levels of most biomarkers (except WBC count and creatine kinase) were significantly higher in the vascular ischaemia group than in the other groups (P < 0·010). However, none of the biomarker levels differed between patients with non-vascular intestinal ischaemia and those with non-ischaemic disease. Receiver operating characteristic (ROC) curve analysis suggested that I-FABP was best at diagnosing vascular intestinal ischaemia (area under the curve 0·88). CONCLUSION: Serum biomarkers may be useful in the diagnosis of vascular, but not non-vascular, intestinal ischaemia. Among them, I-FABP shows promise for detecting vascular ischaemia.


Subject(s)
Fatty Acid-Binding Proteins/metabolism , Intestines/blood supply , Ischemia/diagnosis , Acute Disease , Aged , Aged, 80 and over , Aspartate Aminotransferases/metabolism , Biomarkers/metabolism , C-Reactive Protein/metabolism , Creatine Kinase/metabolism , Early Diagnosis , Female , Fibrin Fibrinogen Degradation Products/metabolism , Humans , L-Lactate Dehydrogenase/metabolism , Lactates/metabolism , Leukocyte Count , Male , Middle Aged , Prospective Studies , ROC Curve
4.
Clin Radiol ; 69(6): 559-66, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24625689

ABSTRACT

AIM: To assess the relationship between thin-section computed tomography (CT) features of primary tumour and high preoperative serum carcinoembryonic antigen (CEA) levels that reportedly suggest poor prognoses in early-stage lung adenocarcinoma. MATERIALS AND METHODS: Two hundred and seventy-five consecutive patients who underwent resection of pathological stage I (T1-2aN0M0) adenocarcinomas with a maximum diameter of ≤ 3 cm (144 men, 131 women; mean age 67.8 years) were enrolled. CT features of the primary tumours and clinical characteristics of these patients were statistically evaluated to identify the factors associated with high serum CEA levels (>5 ng/ml). RESULTS: Eighty-one patients (29.5%) had high serum CEA levels. In univariate analysis, lower ground-glass opacity ratio (p < 0.001), lower tumour shadow disappearance rate (TDR: the ratio of tumour area in mediastinal window to that of lung window, p < 0.001), presence of notch (p = 0.015), and coexistence with bullae or honeycomb cysts (p < 0.001) were observed more frequently in the group with high serum CEA levels than that of the group with normal levels. TDR [odds ratio (OR) 0.984; 95% confidence interval (CI): 0.976-0.993; p < 0.001] and coexistence with bullae or honeycomb cysts (OR = 3.08; 95% CI: 1.55-6.12; p = 0.001) remained significant, even after adjusting patients' age, gender, and smoking status. CONCLUSIONS: Adenocarcinomas with lower TDR and coexisting with bullae or honeycomb cysts are associated with high preoperative serum CEA levels. Although some CEA elevations may be due to benign pulmonary diseases, such tumours are suspected to have poor prognoses, even for early-stage diseases.


Subject(s)
Adenocarcinoma/diagnostic imaging , Carcinoembryonic Antigen/blood , Lung Neoplasms/diagnostic imaging , Adenocarcinoma/blood , Adenocarcinoma of Lung , Adult , Aged , Aged, 80 and over , Female , Humans , Lung Neoplasms/blood , Male , Middle Aged , Multivariate Analysis , Preoperative Care , Prognosis , Retrospective Studies , Tomography, X-Ray Computed
5.
Int J Clin Pract ; 68(6): 700-4, 2014 Jun.
Article in English | MEDLINE | ID: mdl-24905447

ABSTRACT

AIMS: The aim of this study was to examine whether low serum potassium concentration could be a predictor of chronic kidney disease (CKD) in a community-based cohort. MATERIALS AND METHODS: We enrolled 1001 subjects, median period of 5.7 years, and evaluated the risk factors for CKD, defined as estimated glomerular filtration rate (eGFR) < 60 ml/min/1.73 m(2), and assessed whether low serum potassium concentration could predict CKD. RESULTS: Compared with the subjects without development of CKD, age, body mass index, fasting plasma glucose, uric acid (UA), creatinine and serum sodium concentration were higher, and serum potassium concentration was lower in subjects with development of CKD. Univariate Cox regression analyses demonstrated that age, body mass index, fasting plasma glucose, UA, creatinine, serum sodium concentration and serum potassium concentration were associated with progression of CKD. Multiple Cox regression analysis revealed that age, gender, creatinine and serum potassium concentration were independent predictors of CKD after adjustment for covariates. When serum potassium concentration was below 4.0 mmol/l at baseline, hazard ratio (95% confidence interval) of developing CKD was 2.65 (2.04-3.44; p < 0.0001). CONCLUSIONS: Serum potassium concentration could be a clinically relevant risk factor for the progression of CKD, defined as eGFR < 60 ml/min/1.73 m(2) , in healthy subjects.


Subject(s)
Hypokalemia/blood , Renal Insufficiency, Chronic/diagnosis , Adult , Biomarkers/blood , Disease Progression , Female , Humans , Male , Middle Aged , Multivariate Analysis , Potassium/blood , Renal Insufficiency, Chronic/metabolism , Risk Factors
6.
ESMO Open ; 9(8): 103659, 2024 Aug 12.
Article in English | MEDLINE | ID: mdl-39137480

ABSTRACT

BACKGROUND: Adolescents and young adults (AYAs) represent a small proportion of patients with cancer. The genomic profiles of AYA patients with cancer are not well-studied, and outcomes of genome-matched therapies remain largely unknown. PATIENTS AND METHODS: We investigated differences between Japanese AYA and older adult (OA) patients in genomic alterations, therapeutic evidence levels, and genome-matched therapy usage by cancer type. We also assessed treatment outcomes. RESULTS: AYA patients accounted for 8.3% of 876 cases. Microsatellite instability-high and/or tumor mutation burden was less common in AYA patients (1.4% versus 7.7% in OA; P = 0.05). However, BRCA1 alterations were more common in AYA patients with breast cancer (27.3% versus 1.7% in OA; P = 0.01), as were MYC alterations in AYA patients with colorectal cancer (23.5% versus 5.8% in OA; P = 0.02) and sarcoma (31.3% versus 3.4% in OA; P = 0.01). Genome-matched therapy use was similar between groups, with overall survival tending to improve in both. However, in AYA patients, the small number of patients prevented statistical significance. Comprehensive genomic profiling-guided genome-matched therapy yielded encouraging results, with progression-free survival of 9.0 months in AYA versus 3.7 months in OA patients (P = 0.59). CONCLUSION: Our study suggests that tailored therapeutic approaches can benefit cancer patients regardless of age.

7.
Oral Dis ; 19(4): 415-24, 2013 May.
Article in English | MEDLINE | ID: mdl-23034145

ABSTRACT

OBJECTIVE: The aim of this study is to characterize immunohistochemical profiles of lining epithelia of nasopalatine duct cyst (NPC) as well as to correlate those findings with their clinicopathological features to understand the histopathogenesis of NPC. MATERIALS AND METHODS: Forty-one surgical specimens from NPC were examined for clinical profiles and expression of keratin-7, 13, MUC-1, and P63 by immunohistochemistry, compared to radicular cyst (RC) and maxillary sinusitis. RESULTS: Nasopalatine duct cyst was clinically characterized by male predominant occurrence: 44% of the cases involved tooth roots, and 70% with inflammatory backgrounds. Lining epithelia of NPCs without daughter cysts were immunohistochemically distinguished into three layers: a keratin 7-positive (+) ciliated cell layer in the surface, a keratin-13+ middle layer, and a MUC-1+/P63+ lower half, indicating that they were not respiratory epithelia, and the same layering pattern was observed in RC. However, those immunolocalization patterns of the main cyst lining with daughter cyst were exactly the same as those of daughter cyst linings as well as duct epithelia of mucous glands. CONCLUSIONS: Two possible histopathogenesis of NPC were clarified: one was inflammatory cyst like RC and the other was salivary duct cyst-like mucocele.


Subject(s)
Maxillary Diseases/etiology , Nasal Cavity/pathology , Nonodontogenic Cysts/etiology , Nonodontogenic Cysts/pathology , Palate, Hard/pathology , Adult , Aged , Epithelial Cells/pathology , Female , Humans , Inflammation/complications , Keratins/metabolism , Male , Maxillary Diseases/metabolism , Maxillary Diseases/pathology , Maxillary Sinusitis/pathology , Membrane Proteins/metabolism , Middle Aged , Mucins/metabolism , Mucocele/complications , Nonodontogenic Cysts/metabolism , Radicular Cyst/pathology , Sex Ratio , Terminology as Topic , Tooth Root/pathology , Young Adult
8.
J Musculoskelet Neuronal Interact ; 12(2): 74-9, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22647280

ABSTRACT

A randomized controlled trial was conducted to compare the effect of a one-leg standing exercise and a chair-rising exercise on body balance in patients with locomotive disorders. Thirty ambulatory patients (mean age: 66.6 years) were randomly divided into two groups (n=15 in each group): a one-leg standing exercise group and a chair-rising exercise group. All the participants performed calisthenics of the major muscles, a tandem gait exercise, and a stepping exercise. The exercises were performed 3 days per week, and the study period was 5 months. Physical function was evaluated at baseline and at one-month intervals. No significant differences in the baseline characteristics were observed between the two groups. After the 5-month exercise program, the timed up and go, one-leg standing time, and tandem gait time improved significantly in the one-leg standing exercise group, while the walking time and chair-rising time in addition to above parameters improved significantly in the chair-rising exercise group. The improvements in the walking time, chair-rising time, and tandem gait time were significantly greater in the chair-rising exercise group than in the one-leg standing exercise group. The present study showed that the chair-rising exercise was more effective than the one-leg standing exercise for improving walking velocity and dynamic body balance.


Subject(s)
Exercise Therapy/methods , Leg/physiopathology , Movement Disorders/rehabilitation , Physical Fitness/physiology , Postural Balance/physiology , Accidental Falls/prevention & control , Aged , Female , Gait/physiology , Gait Disorders, Neurologic/physiopathology , Gait Disorders, Neurologic/rehabilitation , Humans , Male , Middle Aged , Movement/physiology , Movement Disorders/physiopathology , Muscle Strength/physiology , Muscle Weakness/physiopathology , Muscle Weakness/rehabilitation , Muscle, Skeletal/physiopathology , Recovery of Function/physiology , Treatment Outcome , Walking/physiology
9.
Br Poult Sci ; 53(2): 183-9, 2012.
Article in English | MEDLINE | ID: mdl-22646783

ABSTRACT

1. The aim of this work was to select lactic acid bacteria (LAB) strains from chicks and hens of egg-laying strains for potential use to control Salmonellae. 2. Nineteen LAB strains obtained from culture collections, and 24 strains isolated from excreta of laying hens and chicks, were evaluated for inhibitory capacities against two Salmonella serotypes using a "Spot-the-lawn" technique and other in vitro properties that could be predictive of antimicrobial activity. 3. The size of the inhibition zone differed slightly between Salmonella serotypes, however, the mean size of the Salmonella inhibition zone differed greatly among the LAB strains. Lactobacillus salivarius, L. plantarum, L. rhamnosus and L. reuteri exhibited powerful inhibitory effects to each Salmonella strain. 4. The result of the acid tolerance test showed that all L. salivarius, L. kitasatonis strains and each of L. ingluviei cannot survive in a low pH environment. In the bile acid tolerance assay, growth was inhibited in all strains, except L. kitasatonis HE4, and a large inhibition was observed in most of the L. salivarius and L. crispatus strains. 5. The results demonstrate that some LAB of poultry origin were able to inhibit the growth of Salmonella and survive simulated passage through the gastrointestinal tract. The selected LAB could act in the lower gastrointestinal tract to prevent salmonellosis in poultry.


Subject(s)
Chickens/microbiology , Feces/microbiology , Lactobacillus/physiology , Salmonella enteritidis/growth & development , Salmonella typhimurium/growth & development , Animals , Female , Gastrointestinal Tract/microbiology , Hydrogen-Ion Concentration , Lactobacillus/isolation & purification , Male , Probiotics , Salmonella Infections, Animal/microbiology , Salmonella Infections, Animal/prevention & control
10.
Diabet Med ; 28(1): 96-9, 2011 Jan.
Article in English | MEDLINE | ID: mdl-21210542

ABSTRACT

AIMS: Previous studies have implicated reduced serum bilirubin concentrations in the development of cardiovascular disease. The aim of this study was to examine whether bilirubin may explain the high incidence of vascular complications in haemodialysis patients with Type 2 diabetes. METHODS: We compared serum bilirubin concentrations, as well as other known aetiological risk factors for cardiovascular disease, in 206 Type 2 diabetes patients on haemodialysis with those in 741 Type 2 diabetes patients not receiving haemodialysis, and evaluated the association between serum bilirubin concentration and cardiovascular disease incidence. RESULTS: Incidences of cardiovascular disease and systolic blood pressure were higher; however, BMI and serum total cholesterol were lower in haemodialysis patients compared with those in patients without haemodialysis. Serum total (0.30 ± 0.10 vs. 0.74 ± 0.26 mg/dl, 0.005 ± 0.002 vs. 0.013 ± 0.004 mmol/l, P < 0.0001) and indirect (0.17 ± 0.08 vs. 0.70 ± 0.23 mg/dl, 0.003 ± 0.001 vs. 0.012 ± 0.004 mmol/l, P < 0.0001) bilirubin were lower in haemodialysis patients compared with those in patients without haemodialysis. Stepwise regression analysis demonstrated that age (ß = 0.109, F = 5.959, P < 0.05), duration of diabetes (ß = -0.112, F = 6.048, P < 0.05), sex (ß = -0.123, F = 8.623, P < 0.05), cardiovascular disease events (ß = -0.099, F = 5.131, P < 0.05) and presence of haemodialysis (ß = -0.626, F = 201.727, P < 0.01) were independent factors for serum total bilirubin. Logistic regression demonstrated that age (OR 1.089, 95% CI 1.044-1.136; P < 0.0001), duration of diabetes (OR 1.029, 95% CI 1.001-1.059; P = 0.0423), body mass index (OR 1.115, 95% CI 1.001-1.242; P = 0.0487), habit of smoking (OR 2.445, 95% CI 1.046-5.716; P = 0.0391) and serum total bilirubin (OR 0.192, 95% CI 0.037-0.989; P = 0.0484) were independent factors for cardiovascular disease events. CONCLUSIONS: Low serum bilirubin concentration could be one of the important factors for the high incidence of cardiovascular disease in Type 2 diabetes patients receiving haemodialysis.


Subject(s)
Bilirubin/blood , Cardiovascular Diseases/blood , Diabetes Mellitus, Type 2/blood , Biomarkers/blood , Body Mass Index , Cardiovascular Diseases/etiology , Cardiovascular Diseases/therapy , Diabetes Mellitus, Type 2/complications , Diabetes Mellitus, Type 2/therapy , Female , Humans , Japan , Male , Middle Aged , Prospective Studies , Renal Dialysis , Risk Factors
11.
Eur J Neurol ; 18(9): 1179-83, 2011 Sep.
Article in English | MEDLINE | ID: mdl-21834902

ABSTRACT

BACKGROUND: Nasu-Hakola disease (NHD) is a rare autosomal recessive disorder, characterized by a combination of progressive presenile dementia and formation of multifocal bone cysts, caused by genetic mutations of DAP12 and TREM2, which constitute a receptor/adapter signaling complex expressed on osteoclasts, dendritic cells, macrophages, and microglia. No Japanese patients with TREM2 mutations have been reported previously. METHODS: We reported three siblings affected with NHD in a Japanese family. Amongst them, two died of NHD during the fourth decade of life. The analysis of genomic DNA, cDNA cloning, and western blot of lymphocyte proteins was performed on samples of the living patient. The transcriptome was studied in the autopsied brain of one patient. RESULTS: We identified a homozygous conversion of a single nucleotide T to C at the second position of intron 3 in the splice-donor consensus site (c.482+2T>C) of the TREM2 gene, resulting in exon 3 skipping and aberrant expression of truncated proteins. We identified 136 upregulated genes involved in inflammatory response and immune cell trafficking and 188 downregulated genes including a battery of GABA receptor subunits and synaptic proteins in the patient's brain. CONCLUSIONS: This is the first report of a Japanese NHD family caused by a splicing mutation of TREM2 that induces both neuroinflammation and neurodegeneration.


Subject(s)
Asian People/genetics , Lipodystrophy/genetics , Membrane Glycoproteins/genetics , Osteochondrodysplasias/genetics , Point Mutation , Receptors, Immunologic/genetics , Subacute Sclerosing Panencephalitis/genetics , Adult , Blotting, Western , DNA Mutational Analysis , Family , Female , Humans , Lipodystrophy/pathology , Male , Oligonucleotide Array Sequence Analysis , Osteochondrodysplasias/pathology , Pedigree , Subacute Sclerosing Panencephalitis/pathology
12.
J Exp Med ; 187(3): 389-402, 1998 Feb 02.
Article in English | MEDLINE | ID: mdl-9449719

ABSTRACT

We have demonstrated that intestinal epithelial cells produce interleukin 7 (IL-7), and IL-7 serves as a potent regulatory factor for proliferation of intestinal mucosal lymphocytes expressing functional IL-7 receptor. To clarify the mechanism by which locally produced IL-7 regulates the mucosal lymphocytes, we investigated IL-7 transgenic mice. Here we report that transgenic mice expressing murine IL-7 cDNA driver by the SRalpha promoter developed chronic colitis in concert with the expression of SRalpha/IL-7 transgene in the colonic mucosa. IL-7 transgenic but not littermate mice developed chronic colitis at 4-12 wk of age, with histopathological similarity to ulcerative colitis in humans. Southern blot hybridization and competitive PCR demonstrated that the expression of IL-7 messenger RNA was increased in the colonic mucosal lymphocytes but not in the colonic epithelial cells. IL-7 protein accumulation was decreased in the goblet cell-depleted colonic epithelium in the transgenic mice. Immunohistochemical and cytokine production analysis showed that lymphoid infiltrates in the lamina propria were dominated by T helper cell type 1 CD4+ T cells. Flow cytometric analysis demonstrated that CD4+ intraepithelial T cells were increased, but T cell receptor gamma/delta T cells and CD8alpha/alpha cells were not increased in the area of chronic inflammation. Increased IL-7 receptor expression in mucosal lymphocytes was demonstrated in the transgenic mice. These findings suggest that chronic inflammation in the colonic mucosa may be mediated by dysregulation of colonic epithelial cell-derived IL-7, and this murine model of chronic colitis may contribute to the understanding of the pathogenesis of human inflammatory bowel disease.


Subject(s)
Colitis/genetics , Interleukin-7/metabolism , Intestinal Mucosa/metabolism , Animals , Antigens, CD/immunology , Antigens, CD/metabolism , Blotting, Southern , Colitis/etiology , Colitis/immunology , Colitis/pathology , Cytokines/metabolism , Disease Models, Animal , Flow Cytometry , Gene Expression Regulation/genetics , Humans , Immunohistochemistry , Inflammation/immunology , Interleukin-7/genetics , Interleukin-7/pharmacology , Intestinal Mucosa/pathology , Lymphocytes/immunology , Lymphocytes/metabolism , Mice , Mice, Transgenic , Promoter Regions, Genetic/genetics , RNA, Messenger/analysis , RNA, Messenger/metabolism , Receptors, Interleukin/metabolism , Receptors, Interleukin-7 , T-Lymphocytes, Helper-Inducer/immunology , T-Lymphocytes, Helper-Inducer/metabolism
13.
J Oral Pathol Med ; 39(3): 212-8, 2010 Mar.
Article in English | MEDLINE | ID: mdl-19702869

ABSTRACT

BACKGROUND: Taste dysfunction that develops after radiotherapy for head and neck cancer impairs patients' quality of life. Although taste cells have been shown to degenerate after exposure to X-ray irradiation, the alteration in taste cell population is unclear. This study investigated the histopathological change of taste bud structure and the taste cell population in X-ray irradiated mice. METHODS: The head and neck region of C57BL/6J male mice was exposed to a single 15 Gy dose of X-ray irradiation and a chronological histopathological analysis of the circumvallate papilla was performed. Preference for sweet taste was measured using the two-bottle preference method. RESULTS: The histological analysis of the circumvallate papilla revealed that the basal cells had almost disappeared, but that there was not clear change in the spindle-shaped taste cells on day 4 after irradiation. The number of taste cells had decreased on day 8, and then remained unchanged until day 20, after which they increased and recovered to their original number by day 24. There was a more marked decrease in the number of alpha-gustducin-positive type II taste cells than in the number of serotonin-positive type III taste cells. Preference for sweet taste measured by the two-bottle preference method was decreased in parallel with taste cell number. CONCLUSION: These findings suggest that X-ray irradiation disrupts the basal cells, resulting in a decrease of the number of taste cells, particularly type II taste cells, which may be the cause of radiotherapy-induced taste dysfunction.


Subject(s)
Taste Buds/radiation effects , Taste Disorders/etiology , Animals , Cell Count , Epithelial Cells/pathology , Epithelial Cells/radiation effects , Heterotrimeric GTP-Binding Proteins/analysis , Heterotrimeric GTP-Binding Proteins/radiation effects , Male , Mice , Mice, Inbred C57BL , Mice, Inbred Strains , Nerve Fibers/radiation effects , Nerve Fibers/ultrastructure , Protein Subunits/analysis , Protein Subunits/radiation effects , Radiation Dosage , Sensory Thresholds/radiation effects , Serotonin/analysis , Serotonin/radiation effects , Taste/radiation effects , Taste Buds/pathology , Time Factors , Ubiquitin Thiolesterase/analysis , X-Rays
14.
Clin Nephrol ; 73(1): 30-5, 2010 Jan.
Article in English | MEDLINE | ID: mdl-20040349

ABSTRACT

AIMS: To determine the metal ion and vitamin in vitro adsorption profile of sevelamer hydrochloride (sevelamer-HCl) and colestilan(INN)/colestimide(JAN), a novel ion-exchange resin being developed as a phosphate binder for end-stage renal disease (ESRD) patients undergoing hemodialysis, adsorption of metal ions (iron, cobalt, copper and zinc) and vitamins (B6, B12, C, K and folic acid) essential for hematopoiesis/blood coagulation was assessed. METHODS: Mixtures of each resin (colestilan or sevelamer-HCl, 4 mg/ml) and metal ions (Fe(III), Fe(II), Co(II), Cu(II), and Zn(II), 1 microg/ml) were adjusted to pH 1.2 or 6.8 and incubated at 37 degrees C for 1 hour. Metal ions in the recovered filtrate were detected by inductively coupled plasma optical emission spectrometry. In addition, the mixtures of each resin (4 mg/ml) and vitamins (B6, B12, C, K and folic acid, 0.5 - 250 microg/ml) were adjusted to pH 6.8 and incubated at 37 degrees C for 0.5 hour. The vitamin concentrations in the recovered filtrate were quantified by HPLC. RESULTS: Colestilan did not adsorb any metals tested at either pH level, whereas sevelamer-HCl adsorbed copper(II) and zinc(II) ion at pH 6.8 with adsorption ratios of 99% and 38%, respectively. Both resins showed almost complete adsorption of vitamin C, vitamin K, and folic acid, but weak adsorption of vitamin B6, and no adsorption of vitamin B12. CONCLUSIONS: The differing adsorption profiles for metal ions and vitamins between sevelamer-HCl and colestilan may be of importance for the individualized management of anemia and malnutrition in chronic hemodialysis patients receiving phosphate binding ion-exchange resins for the control of hyperphosphatemia.


Subject(s)
Cations/chemistry , Ion Exchange Resins/chemistry , Metals, Heavy/chemistry , Vitamins/chemistry , Adsorption , Bile Acids and Salts/chemistry , Polyamines/chemistry , Sevelamer
15.
Int J Oral Maxillofac Surg ; 49(10): 1290-1293, 2020 Oct.
Article in English | MEDLINE | ID: mdl-32371177

ABSTRACT

Ectomesenchymal chondromyxoid tumour (ECT) is an extremely rare intraoral mesenchymal tumour. Most of these tumours have been identified on the anterior aspect of the dorsal surface of the tongue. ECT is difficult to diagnose because of its rarity. We report a case of ECT arising on the lateral border of the tongue in a 67-year-old woman. The tumour, measuring 20 × 10 mm in size, was surgically removed. Histopathologically, the tumour was composed of small polygonal cells arranged in sheets, with a myxoid or hyalinized stroma. The tumour boundary was clear; however, the tumour showed a multinodular structure expanding along the tongue surface without obvious capsule. Careful examination revealed the tumour nodule to be spreading in a skip lesion-like fashion away from the main part of the tumour in the striated muscle layer. Although there was no evidence of recurrence at 18 months after the surgery, our observations suggest that surgery for ECT resection with a safety margin is more appropriate than enucleation.


Subject(s)
Mesenchymoma , Myoepithelioma , Tongue Neoplasms , Aged , Female , Humans , Mesenchymoma/diagnostic imaging , Mesenchymoma/surgery , Neoplasm Recurrence, Local , Tongue , Tongue Neoplasms/diagnostic imaging , Tongue Neoplasms/surgery
16.
Int J Oral Maxillofac Surg ; 49(8): 984-992, 2020 Aug.
Article in English | MEDLINE | ID: mdl-32070653

ABSTRACT

The objectives of this study were to evaluate survival in 141 patients with stage II-IV oral squamous cell carcinoma (OSCC) treated with preoperative intra-arterial chemotherapy with docetaxel, cisplatin, and peplomycin combined with intravenous chemotherapy using 5-fluorouracil (IADCPIVF) via the superficial temporal artery, and to clarify the prognostic factors. The study population included 59 patients with stage II OSCC, 34 with stage III, and 48 with stage IV. After IADCPIVF, 139 patients underwent surgery; minimally invasive surgeries (MIS) including excisional biopsy were performed on 96 patients with a remarkably good response to IADCPIVF. The primary tumour response rate was 99.3% (complete response rate 56.7%, good partial response rate 17.0%, fair partial response rate 25.5%). Additionally, there were no serious adverse events associated with IADCPIVF. The 5-year overall survival rate was 74.6% (stage II 83.6%, stage III 72.7%, stage IV 64.8%). In the multivariate analysis of survival, T classification and clinical tumour response were significant prognostic factors. Eight (8.3%) of the patients who received MIS had primary recurrence and six were salvaged. In conclusion, IADCPIVF is safe and efficacious for treating OSCC, and MIS could reduce the extent of primary tumour resection in the case of a remarkably good response.


Subject(s)
Carcinoma, Squamous Cell , Mouth Neoplasms/drug therapy , Antineoplastic Combined Chemotherapy Protocols , Cisplatin/therapeutic use , Docetaxel , Fluorouracil , Humans , Neoplasm Recurrence, Local , Peplomycin/therapeutic use , Taxoids/therapeutic use
17.
Horm Metab Res ; 41(7): 548-53, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19280551

ABSTRACT

mu-Crystallin is an NADPH-dependent cytosolic T3-binding protein. A knockout study in mice showed that mu-crystallin has a physiological function as a reservoir of T3 in the cytoplasm in vivo. Patients with nonsyndromic deafness were reported to have point mutations in the mu-crystallin gene. The expression of mu-crystallin is regulated by multiple factors. The present study was performed to determine whether thyroid function is related to the expression of mu-crystallin mRNA in peripheral mononuclear cells. We examined 23 normal healthy male and female subjects and 15 patients with Graves' disease. mu-Crystallin protein expression was determined immunohistochemically in peripheral mononuclear cells. The expression of mu-crystallin mRNA was assessed by reverse transcription of total RNA from peripheral mononuclear cells followed by quantitative PCR. mu-Crystallin protein was detected in peripheral mononuclear cells. The mRNA expression was negatively correlated with age in normal female subjects. The values in female subjects were significantly higher than those in males. The values were positively correlated with serum TSH concentration. The values of the thyrotoxic patients with Graves' disease were lower than those in healthy subjects. A transient increase in mu-crystallin expression was observed within 14-42 days after the initial treatment with antithyroid medication. Thyroid hormone inversely relates to the expression of mu-crystallin mRNA in euthyroid mononuclear cells. Abrupt suppression of thyroid function leads to overexpression of mu-crystallin mRNA in thyrotoxic mononuclear cells. Thyroid hormone-regulated mu-crystallin expression may control thyroid hormone action via the intracytoplasmic T (3) capacity.


Subject(s)
Antithyroid Agents/therapeutic use , Crystallins/genetics , Gene Expression/drug effects , Graves Disease/drug therapy , Methimazole/therapeutic use , Adult , Age Factors , Cells, Cultured , Crystallins/metabolism , Female , Graves Disease/genetics , Graves Disease/metabolism , Humans , Leukocytes, Mononuclear/metabolism , Male , Middle Aged , RNA, Messenger/genetics , RNA, Messenger/metabolism , Sex Factors , Thyroid Function Tests , Thyroid Hormones/blood , mu-Crystallins
18.
J Oral Pathol Med ; 38(4): 348-55, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19239574

ABSTRACT

BACKGROUND: As one of the valuable tools for differential diagnoses of oral epithelial dysplasia, carcinoma in situ (CIS) and squamous cell carcinoma (SCC), we have proposed the immunohistochemistry for perlecan, a heparan sulfate proteoglycan (HSPG). As HSPGs have been shown to be extracellular docking molecules for matrix metalloproteinase (MMP) 7, our aim was to determine the expression mode of MMP-7 in these lesions for its possible diagnostic aid for oral borderline malignancies. METHODS: Twenty cases each of moderate dysplasia, CIS, SCC, and normal/hyperplastic/mild dysplastic epithelia of the tongue and buccal mucosa were immunohistochemically examined for MMP-1, -2 and -7 in reference to their perlecan immunolocalization. RESULTS: The expression of all three MMPs in the normal mucosal epithelium was restricted mainly to the parabasal layers. The most striking finding was strong expression of MMP-7 in epithelial dysplasia with a two-phase appearance: a clear demarcation of MMP-7-immunopositive (+) lower dysplastic/basaloid cells from non-positive upper keratinized cells. MMP-7+ cells were spread over the whole epithelial layer of CIS. In SCC, MMP-7 positivity was reduced from carcinoma cells but instead appeared in stromal cells. These expression profiles of MMP-7 resembled those of perlecan. MMP-1 and MMP-2 exhibited a similar but much weaker staining than MMP-7. CONCLUSION: These results suggest that the enhanced metabolism of perlecan associated with MMP-7 plays an important role in the cell proliferation of oral epithelia in their malignant transformation process, and that MMP-7 immunohistochemistry may be a valuable aid for identification of the cell proliferation center in oral CIS and dysplasia.


Subject(s)
Carcinoma in Situ/metabolism , Carcinoma, Squamous Cell/metabolism , Cell Transformation, Neoplastic/metabolism , Heparan Sulfate Proteoglycans/metabolism , Matrix Metalloproteinase 7/biosynthesis , Precancerous Conditions/metabolism , Tongue Neoplasms/metabolism , Carcinoma in Situ/diagnosis , Carcinoma, Squamous Cell/diagnosis , Cell Proliferation , Diagnosis, Differential , Epithelial Cells/metabolism , Epithelial Cells/pathology , Humans , Immunohistochemistry , Matrix Metalloproteinase 1/biosynthesis , Matrix Metalloproteinase 2/biosynthesis , Precancerous Conditions/diagnosis , Tongue Neoplasms/diagnosis
19.
J Chem Phys ; 131(11): 114309, 2009 Sep 21.
Article in English | MEDLINE | ID: mdl-19778115

ABSTRACT

Benzene and fluorobenzene molecules were multiply ionized through Auger decay following from the C 1s or the F 1s photoionization and their subsequent dissociations were studied utilizing position-sensitive time-of-flight measurements. The angular correlation between the momenta of (H(+)-H(+)) and (H(+)-F(+)) fragment ions derived from the multiply ionized benzene or fluorobenzene clearly reflects the hexagonal structure of the parent molecules, though the dissociations are not described by the simple Coulomb explosion model. Also, analysis on the planarity between the momentum of H(+), C(+), and F(+) reveals that these three ions are emitted almost in a single plane.

20.
Eur J Gynaecol Oncol ; 30(2): 155-61, 2009.
Article in English | MEDLINE | ID: mdl-19480244

ABSTRACT

PURPOSE OF INVESTIGATION: The clinical characteristics and long-term prognostic factors of borderline ovarian tumors (BOTs) were evaluated. METHODS: Data from patients who were treated for BOTs in the Kinki District of Japan from 1990 to 2006 were revieved. Two hundred and twenty-two cases were retrospectively investigated for stage, surgical procedure, histopathological features, adjuvant chemotherapy and prognosis. RESULTS: FIGO stages included 212 patients with Stage I disease, three with Stage II and seven with Stage III. One hundred and sixty-nine cases were diagnosed as mucinous tumor, 47 were serous, and six were others. Radical surgery was performed in 136 patients and conservative surgery in 86 patients. Only two patients showed invasive peritoneal implants. Forty patients received adjuvant chemotherapy. The survival rate was 95% at ten-years. Statistical analysis showed that earlier stage, absence of residual tumors, peritoneal implants, ovarian stromal involvement, and negative peritoneal cytology were associated with significantly better overall survival. CONCLUSION: The prognosis of patients with BOT is excellent. There are insufficient data to support a role for aggressive surgery and adjuvant chemotherapy for the possibility of prolonged survival.


Subject(s)
Ovarian Neoplasms/mortality , Adolescent , Adult , Aged , Female , Humans , Middle Aged , Ovarian Neoplasms/pathology , Ovarian Neoplasms/therapy , Prognosis , Survival Analysis , Survival Rate , Treatment Outcome , Young Adult
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