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1.
BMC Oral Health ; 17(1): 46, 2017 Jan 16.
Article in English | MEDLINE | ID: mdl-28093069

ABSTRACT

BACKGROUND: The diagnosis of the progression of periodontitis presently depends on the use of clinical symptoms (such as attachment loss) and radiographic imaging. The aim of the multicenter study described here was to evaluate the diagnostic use of the bacterial content of subgingival plaque recovered from the deepest pockets in assessing disease progression in chronic periodontitis patients. METHODS: This study consisted of a 24-month investigation of a total of 163 patients with chronic periodontitis who received trimonthly follow-up care. Subgingival plaque from the deepest pockets was recovered and assessed for bacterial content of Porphyromonas gingivalis, Prevotella intermedia, and Aggregatibacter actinomycetemcomitans using the modified Invader PLUS assay. The corresponding serum IgG titers were measured using ELISA. Changes in clinical parameters were evaluated over the course of 24 months. The sensitivity, specificity, and prediction values were calculated and used to determine cutoff points for prediction of the progression of chronic periodontitis. RESULTS: Of the 124 individuals who completed the 24-month monitoring phase, 62 exhibited progression of periodontitis, whereas 62 demonstrated stable disease. The P. gingivalis counts of subgingival plaque from the deepest pockets was significantly associated with the progression of periodontitis (p < 0.001, positive predictive value = 0.708). CONCLUSIONS: The P. gingivalis counts of subgingival plaque from the deepest pockets may be associated with the progression of periodontitis.


Subject(s)
Chronic Periodontitis/diagnosis , Chronic Periodontitis/microbiology , Dental Plaque/microbiology , Saliva/microbiology , Aged , Antigens, Bacterial/blood , Chronic Periodontitis/therapy , Colony Count, Microbial , Disease Progression , Enzyme-Linked Immunosorbent Assay , Female , Humans , Immunoglobulin G/blood , Japan , Male , Middle Aged , Prospective Studies
2.
J Periodontal Res ; 51(6): 768-778, 2016 Dec.
Article in English | MEDLINE | ID: mdl-26791469

ABSTRACT

BACKGROUND AND OBJECTIVE: A diagnosis of periodontitis progression is presently limited to clinical parameters such as attachment loss and radiographic imaging. The aim of this multicenter study was to monitor disease progression in patients with chronic periodontitis during a 24-mo follow-up program and to evaluate the amount of bacteria in saliva and corresponding IgG titers in serum for determining the diagnostic usefulness of each in indicating disease progression and stability. MATERIAL AND METHODS: A total of 163 patients with chronic periodontitis who received trimonthly follow-up care were observed for 24 mo. The clinical parameters and salivary content of Porphyromonas gingivalis, Prevotella intermedia and Aggregatibacter actinomycetemcomitans were assessed using the modified Invader PLUS assay, and the corresponding serum IgG titers were measured using ELISA. The changes through 24 mo were analyzed using cut-off values calculated for each factor. One-way ANOVA or Fisher's exact test was used to perform between-group comparison for the data collected. Diagnostic values were calculated using Fisher's exact test. RESULTS: Of the 124 individuals who completed the 24-mo monitoring phase, 62 exhibited periodontitis progression, whereas 62 demonstrated stable disease. Seven patients withdrew because of acute periodontal abscess. The ratio of P. gingivalis to total bacteria and the combination of P. gingivalis counts and IgG titers against P. gingivalis were significantly related to the progression of periodontitis. The combination of P. gingivalis ratio and P. gingivalis IgG titers was significantly associated with the progression of periodontitis (p = 0.001, sensitivity = 0.339, specificity = 0.790). CONCLUSIONS: It is suggested that the combination of P. gingivalis ratio in saliva and serum IgG titers against P. gingivalis may be associated with the progression of periodontitis.


Subject(s)
Antibodies, Bacterial/blood , Chronic Periodontitis/pathology , Immunoglobulin G/blood , Saliva/microbiology , Aggregatibacter actinomycetemcomitans , Bacterial Load , Bacteroidaceae Infections/microbiology , Bacteroidaceae Infections/pathology , Chronic Periodontitis/blood , Chronic Periodontitis/metabolism , Disease Progression , Enzyme-Linked Immunosorbent Assay , Female , Humans , Male , Middle Aged , Pasteurellaceae Infections/microbiology , Pasteurellaceae Infections/pathology , Porphyromonas gingivalis , Prevotella intermedia , Prospective Studies
3.
Kyobu Geka ; 58(4): 337-40, 2005 Apr.
Article in Japanese | MEDLINE | ID: mdl-15828258

ABSTRACT

We report a case of a 27-year-old woman with primary neurogenous sarcoma of the lung. She had no symptoms but an abnormal shadow of the right lower lung field on the chest X-ray. Chest computed tomography (CT) revealed a well defined round mass, 20 mm in maximum diameter, at the right S9. Pathological study of the specimen obtained by CT-guided percutaneous needle biopsy showed undefferentiated carcinoma. Positron emission tomography (PET) disclosed intensely increased uptake of fluoro-2-deoxy-D-glucose (FDG) at the lung lesion without other abnormal uptakes. The patient underwent right lower lobectomy of the lung and mediastinal lymph nodes dissection. Results from immunohistological study yielded a definitive diagnosis of neurogenous sarcoma. Postoperative course was uneventful, and there has been no evidence of recurrence and metastasis for more than a year after the surgery. Reported cases of primary neurogenous sarcoma of the lung are reviewed.


Subject(s)
Lung Neoplasms/surgery , Neurofibrosarcoma/surgery , Pneumonectomy , Adult , Female , Humans , Lung Neoplasms/diagnostic imaging , Lymph Node Excision , Neurofibrosarcoma/diagnostic imaging , Pneumonectomy/methods , Tomography, X-Ray Computed
4.
J Control Release ; 52(1-2): 119-29, 1998 Mar 02.
Article in English | MEDLINE | ID: mdl-9685942

ABSTRACT

The delivery ability of a pressure-controlled colon delivery capsule (PCDC) containing caffeine as a test drug was evaluated after oral administration to healthy male human volunteers. The driving force causing PCDC disintegration in the intestinal tract is the physiological luminal pressure which results from peristalsis. Three kinds of PCDCs having different thickness of a water-insoluble polymer membrane was prepared by coating the inner surface of the gelatin capsules with ethylcellulose (EC). The mean thickness were 40 +/- 1 (SE) for type 1, 44 +/- 1 for type 2 and 50 +/- 1 micron for type 3 PCDC, respectively. Caffeine was dissolved with a suppository base (PEGs 400 and 1000) and the capsules were filled. Doses were 15, 45 or 75 mg. After blank saliva samples were obtained, test preparations were orally administered to the volunteers and saliva samples were collected for 1 min intervals hourly from 1 to 10 h in the fasted state study, and from 1 to 20 h and at 25 h in the fed state study. Caffeine concentrations in the saliva samples were analyzed by HPLC. The maximum salivary caffeine excretion rate increased as the oral caffeine dose increased. The maximum salivary caffeine excretion rate increased predominantly compared to the pre-dose level in 75 mg dose study. Therefore, all following studies were performed with this dose. The first appearance time of caffeine into the saliva, TI, was used as a parameter to estimate the disintegration time of test preparations in the gastrointestinal tract. The mean TI of types 1, 2, and 3 PCDCs were 3.0 +/- 0.4, 4.0 +/- 0.4 and 4.5 +/- 0.3 h, respectively. After oral administration of 75 mg caffeine in pain gelatin capsule as a reference preparation, caffeine appeared in the saliva within 0.5 h. The mean hardness of the PCDCs were 1.05 +/- 0.10 (type 1), 1.55 +/- 0.06 (type 2) and 2.08 +/- 0.15 newton (type 3), respectively. There were good correlations between three parameters: EC coating membrane thickness, hardness and TI (determination coefficient r2 = 0.935 between TI and thickness, r2 = 0.998 between thickness and hardness, r2 = 0.958 between hardness and TI). The effect of food intake on the delivery ability was examined with type 3 PCDCs. Food intake prolonged the mean TI, from 4.5 +/- 0.3 to 7.8 +/- 1.3 h. This increase is thought to be ascribed to prolonged gastric emptying time. Comparison with reported colon arrival times indicates that the type 3 PCDC functions in colon delivery of caffeine and is thought to be applicable to other drugs.


Subject(s)
Caffeine/administration & dosage , Colon/metabolism , Drug Delivery Systems , Adult , Caffeine/pharmacokinetics , Capsules , Cellulose/administration & dosage , Cellulose/analogs & derivatives , Dose-Response Relationship, Drug , Food , Humans , Male , Pressure , Saliva/metabolism
5.
Intern Med ; 31(2): 260-4, 1992 Feb.
Article in English | MEDLINE | ID: mdl-1376179

ABSTRACT

A 45-year-old woman who underwent gastrectomy for gastric carcinoma which had metastasized to the liver and ovaries, showed high serum levels of hCG, AFP and CEA. To locate the source, an immunohistochemical technique was utilized. HCG-producing cells were detected in poorly differentiated adenocarcinoma of a primary tumor and an ovarian metastatic site, and AFP-producing cells in poorly differentiated adenocarcinoma forming a medullary pattern of primary site and metastatic foci. CEA-producing cells were found diffused in primary tumor and metastatic foci. From the viewpoint of oncodevelopmental gene expression (Cancer Res 36:3423, 1976), it is interesting that the serum levels of these three tumor markers (hCG, AFP, CEA) were elevated simultaneously.


Subject(s)
Carcinoembryonic Antigen/blood , Chorionic Gonadotropin/blood , Stomach Neoplasms/blood , alpha-Fetoproteins/metabolism , Biomarkers, Tumor/blood , Female , Hormones, Ectopic/blood , Humans , Liver Neoplasms/blood , Liver Neoplasms/immunology , Liver Neoplasms/secondary , Middle Aged , Ovarian Neoplasms/blood , Ovarian Neoplasms/immunology , Ovarian Neoplasms/secondary , Stomach Neoplasms/immunology , Stomach Neoplasms/pathology
6.
Acta Pathol Jpn ; 40(11): 845-50, 1990 Nov.
Article in English | MEDLINE | ID: mdl-1706556

ABSTRACT

A case of malignant mixed müllerian tumor of the ovary in a 57-year-old woman is reported along with the results of an immunohistochemical study. The tumor, measuring 16 x 10 x 9 cm, was composed predominantly of adenocarcinoma with a smaller amount of anaplastic carcinoma as an epithelial component and chondrosarcoma, liposarcoma, fibrosarcoma and rhabdomyoblasts as mesenchymal elements. Immunohistochemistry using paraffin sections demonstrated cytokeratin (CK) and epithelial membrane antigen (EMA), generally regarded as epithelial markers, not only in the epithelial component but also in chondrosarcoma cells. Vimentin and desmin, generally regarded as mesenchymal markers, were exhibited partly in carcinoma cells as well as in mesenchymal elements. Positive staining for S-100 protein was obtained not only in chondrosarcoma and liposarcoma cells, but also partly in adenocarcinoma cells. This intricate immunohistochemical picture reflected the histologic findings. It is noteworthy that both carcinoma cells and chondrosarcoma cells demonstrated simultaneous expression of CK, EMA, vimentin, desmin and S-100 protein. This somewhat unusual antigen expression by tumor cells may indicate a change in the nature of tumor cells due to microenvironmental factors.


Subject(s)
Neoplasms, Germ Cell and Embryonal/pathology , Ovarian Neoplasms/pathology , Adenocarcinoma/metabolism , Adenocarcinoma/pathology , Chondrosarcoma/metabolism , Chondrosarcoma/pathology , Chorionic Gonadotropin/metabolism , Desmin/metabolism , Female , Fibrosarcoma/metabolism , Fibrosarcoma/pathology , Humans , Immunohistochemistry , Keratins/metabolism , Liposarcoma/metabolism , Liposarcoma/pathology , Membrane Glycoproteins/metabolism , Middle Aged , Mucin-1 , Myoglobin/metabolism , Neoplasms, Germ Cell and Embryonal/metabolism , Ovarian Neoplasms/metabolism , Rhabdomyoma/metabolism , Rhabdomyoma/pathology , S100 Proteins/metabolism , Vimentin/metabolism , alpha-Fetoproteins/metabolism
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