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1.
Hypertens Res ; 24(5): 523-9, 2001 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-11675946

RESUMO

We evaluated the association between the phenotypes or alleles of apolipoprotein E and hypertension in Japanese-Americans living in Hawaii or Los Angeles. The study consisted of 932 nondiabetic participants aged 40-79 years. Of these participants, 315 were hypertensive, while the remainder were normotensive. The prevalence of hypertension was higher in subjects with the e2 allele than in those without. Using a multivariable prediction model that included age, serum glucose, insulin, lipids, and body mass index, we found the epsilon2 allele to be associated with hypertension in men (odds ratio (OR), 1.53; 95% confidence interval (CI), 1.05-2.24) and for both sexes combined (OR, 1.35; 95% CI, 1.05-1.73). In a follow-up study, 37 of the 352 (11%) normotensive subjects had developed hypertension 4 years after the baseline examination. The frequencies of the apolipoprotein E phenotype E3/2 and the epsilon2 allele were higher in the subjects who became hypertensive than in those who remained normotensive. The E3/2 phenotype was associated with incidence of hypertension after adjustment for age, sex, baseline body mass index, and systolic blood pressure (OR, 1.75; 95% CI, 1.01-2.90). When serum lipids, glucose, and insulin were included in this analysis, the E3/2 phenotype tended to be associated with the incidence of hypertension. In conclusion, the epsilon2 allele of apolipoprotein E was associated with hypertension in Japanese-Americans. This association may be mediated via high levels of serum triglycerides that in turn are mediated in part by the epsilon2 allele. Nonlipid mechanisms may also be responsible for the effect of the epsilon2 allele on hypertension.


Assuntos
Apolipoproteínas E/genética , Hipertensão/epidemiologia , Hipertensão/genética , Idoso , Apolipoproteína E2 , Apolipoproteína E3 , Pressão Sanguínea , Feminino , Seguimentos , Havaí/epidemiologia , Humanos , Hiperlipidemias/epidemiologia , Hiperlipidemias/genética , Japão/epidemiologia , Los Angeles/epidemiologia , Masculino , Pessoa de Meia-Idade , Fenótipo , Fatores de Risco
2.
Hypertens Res ; 24(5): 531-6, 2001 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-11675947

RESUMO

The present study was to assess the association of metabolic factors including hyperinsulinemia, with the development of hypertension in Japanese-Americans. One hundred forty normotensive (<140/90 mmHg) subjects aged 40 to 69 years old from the Hawaii-Los Angeles-Hiroshima study were followed for 15 years. Patients with cardiovascular disease were excluded. Body mass index (BMI), blood pressure (BP), serum total cholesterol (TC), triglycerides (TG), uric acid (UA), and glucose and insulin responses at baseline, 1 h, and 2 h after a glucose load were analyzed. Seventeen subjects became hypertensive (systolic BP > or = 160 mmHg, diastolic BP > or = 95 mmHg, or received drug treatment) during follow-up. Age- and sex-adjusted BMI, BP, serum UA, TG, insulin, and changes in fasting glucose during follow-up were higher in subjects who later became hypertensive than in those who did not. There was no difference in the change in BMI. Age- and sex-adjusted relative risks for the development of hypertension by quartiles of BMI, serum UA, TG, and the sum of insulin values (sigmainsulin) during a glucose load were highest in highest quartile of the distribution. When age, sex, systolic BP, BMI, serum UA, TC, TG, fasting glucose, sigmainsulin, and the change in BMI were used in a proportional hazard analysis, hyperinsulinemia, hyperuricemia, and systolic BP were found to be significant risk factors for hypertension. In conclusion, hyperinsulinemia, as well as obesity, hyperuricemia, and hypertriglyceridemia were associated with hypertension in Japanese-Americans. Hyperinsulinemia and hyperuricemia were independent predictors of the development of hypertension.


Assuntos
Hiperinsulinismo/epidemiologia , Hipertensão/epidemiologia , Glicemia , Pressão Sanguínea , Índice de Massa Corporal , Colesterol/sangue , Feminino , Havaí/epidemiologia , Humanos , Hiperinsulinismo/sangue , Hipertensão/sangue , Insulina/sangue , Resistência à Insulina , Japão/epidemiologia , Los Angeles/epidemiologia , Masculino , Pessoa de Meia-Idade , Obesidade/epidemiologia , Modelos de Riscos Proporcionais , Triglicerídeos/sangue , Ácido Úrico/sangue
3.
N Engl J Med ; 345(11): 784-9, 2001 Sep 13.
Artigo em Inglês | MEDLINE | ID: mdl-11556297

RESUMO

BACKGROUND: Although many studies have found an association between Helicobacter pylori infection and the development of gastric cancer, many aspects of this relation remain uncertain. METHODS: We prospectively studied 1526 Japanese patients who had duodenal ulcers, gastric ulcers, gastric hyperplasia, or nonulcer dyspepsia at the time of enrollment; 1246 had H. pylori infection and 280 did not. The mean follow-up was 7.8 years (range, 1.0 to 10.6). Patients underwent endoscopy with biopsy at enrollment and then between one and three years after enrollment. H. pylori infection was assessed by histologic examination, serologic testing, and rapid urease tests and was defined by a positive result on any of these tests. RESULTS: Gastric cancers developed in 36 (2.9 percent) of the infected and none of the uninfected patients. There were 23 intestinal-type and 13 diffuse-type cancers. Among the patients with H. pylori infection, those with severe gastric atrophy, corpus-predominant gastritis, and intestinal metaplasia were at significantly higher risk for gastric cancer. We detected gastric cancers in 21 (4.7 percent) of the 445 patients with nonulcer dyspepsia, 10 (3.4 percent) of the 297 with gastric ulcers, 5 (2.2 percent) of the 229 with gastric hyperplastic polyps, and none of the 275 with duodenal ulcers. CONCLUSIONS: Gastric cancer develops in persons infected with H. pylori but not in uninfected persons. Those with histologic findings of severe gastric atrophy, corpus-predominant gastritis, or intestinal metaplasia are at increased risk. Persons with H. pylori infection and nonulcer dyspepsia, gastric ulcers, or gastric hyperplastic polyps are also at risk, but those with duodenal ulcers are not.


Assuntos
Infecções por Helicobacter/complicações , Helicobacter pylori , Neoplasias Gástricas/etiologia , Adulto , Idoso , Intervalo Livre de Doença , Úlcera Duodenal/complicações , Dispepsia/complicações , Feminino , Gastrite/complicações , Infecções por Helicobacter/diagnóstico , Humanos , Hiperplasia/complicações , Masculino , Pessoa de Meia-Idade , Pólipos/complicações , Estudos Prospectivos , Estômago/patologia , Úlcera Gástrica/complicações
5.
Scand J Urol Nephrol ; 35(2): 141-6, 2001 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-11411658

RESUMO

OBJECTIVE: The aim of this study was to investigate the mechanism underlying the increase of serum soluble interleukin-2 receptor (IL-2R) levels in patients on continuous ambulatory peritoneal dialysis. MATERIAL AND METHODS: In 13 dialysis patients and 17 healthy controls, serum soluble IL-2R levels were determined by enzyme-linked immunosorbent assay, and CD25-positive (cell surface IL-2R-positive) cells were detected by flow cytometry. Soluble IL-2R levels were also measured in the supernatant of cultured peripheral blood mononuclear cells. RESULTS: The serum soluble IL-2R level was significantly higher in the patients than in the healthy controls (p < 0.0001). In contrast, both the percentage and the absolute count of CD25-positive cells showed no significant differences, and neither did the soluble IL-2R level in culture supernatant. Serum soluble IL-2R levels showed a positive correlation with the serum beta2-microglobulin level (p < 0.01), the age of the patients (p < 0.05), and duration of dialysis (p < 0.05), as well as a negative correlation with the urine volume (p < 0.05). CONCLUSIONS: The increase of serum soluble IL-2R in patients on peritoneal dialysis may be caused by accumulation due to its low transperitoneal clearance and low urinary excretion.


Assuntos
Falência Renal Crônica/sangue , Falência Renal Crônica/terapia , Diálise Peritoneal Ambulatorial Contínua , Receptores de Interleucina-2/sangue , Adulto , Feminino , Humanos , Masculino
6.
Pharmacogenetics ; 11(3): 275-8, 2001 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-11337944

RESUMO

Polymorphisms at three loci in the thiopurine methyltransferase (TPMT) gene are known to be responsible for azathioprine and 6-mercaptopurine (6MP) toxicity. Among them, only TPMT*3C variant allele with A719G mutation was found in 15/522 (2.9%; 17/1044 alleles; 1.6%) Japanese individuals including two homozygotes. The allele frequency was different from that in Caucasians, and investigation of TPMT polymorphisms with consideration of ethnic differences before administration of azathioprine or 6MP may provide clinically useful information.


Assuntos
Alelos , Povo Asiático/genética , Genética Populacional , Metiltransferases/genética , Polimorfismo Genético , Primers do DNA/química , Frequência do Gene , Genótipo , Humanos , Japão/epidemiologia , Reação em Cadeia da Polimerase , População Branca/genética
7.
Nihon Kokyuki Gakkai Zasshi ; 39(1): 35-9, 2001 Jan.
Artigo em Japonês | MEDLINE | ID: mdl-11296384

RESUMO

Routine chest radiography demonstrated abnormal opacities in the right lower lung field of a 54-year-old man with idiopathic interstitial pneumonia. A high-resolution chest CT scan showed diffuse air-space consolidation in the right lower lung with replacement of a honeycomb area. The diagnosis was adenocarcinoma, and a right lower lobectomy was performed. Histopathologic examination showed moderately differentiated adenocarcinoma and the pathological stage was T3 N0 M0 (Stage IIB). About 1 year later, the cancer recurred with diffuse air-space consolidation in the whole of the right lung and the left middle and lower lung, which resulted in the patient's death. It was difficult to discriminate between an acute change for the worse of idiopathic interstitial pneumonia and a recurrence of lung cancer on the basis of the CT findings in this patient. It is important to elucidate the CT features of lung cancer associated with idiopathic interstitial pneumonia.


Assuntos
Adenocarcinoma/diagnóstico por imagem , Doenças Pulmonares Intersticiais/complicações , Neoplasias Pulmonares/diagnóstico por imagem , Adenocarcinoma/etiologia , Adenocarcinoma/patologia , Diagnóstico Diferencial , Evolução Fatal , Humanos , Pulmão/diagnóstico por imagem , Pulmão/patologia , Doenças Pulmonares Intersticiais/diagnóstico por imagem , Doenças Pulmonares Intersticiais/patologia , Neoplasias Pulmonares/etiologia , Neoplasias Pulmonares/patologia , Masculino , Pessoa de Meia-Idade , Recidiva Local de Neoplasia , Risco , Tomografia Computadorizada por Raios X
8.
Respirology ; 6(1): 27-35, 2001 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-11264760

RESUMO

OBJECTIVE: The aim of the study was to compare the efficacy and safety of budesonide Turbuhaler with that of beclomethasone dipropionate (BDP) pMDI. METHODOLOGY: Three hundred and fifty adult asthma patients (mean age 52.7 years, mean baseline morning peak expiratory flow (PEF) 294 L/min (< 80% predicted normal)), taking BDP via pressurized metered-dose inhaler (pMDI), 400 microg daily for at least 2 months, were randomized in an open 6 week study to receive daily doses of either budesonide 100 microg or 400 microg twice daily via Turbuhaler or continued treatment with BDP, 100 microg four times daily. The primary efficacy variable was the mean change in morning PEF from baseline to the end of treatment. Outcome was also assessed using symptom scores and investigators' assessments employed in Japanese clinical trials. RESULTS: At the end of the 6 week treatment period, mean morning PEF improved significantly from baseline in both budesonide groups, 16 L/min and 33 L/min in the 200 microg and 800 microg groups, respectively, but not in the BDP group, 5 L/min. There was no significant difference between 200 microg budesonide and 400 microg BDP treatment in the effect on PEF (P = 0.29), but 800 microg budesonide was significantly superior to BDP (P < 0.001). Final assessment of improvement and usefulness ratings showed that both budesonide treatments were significantly superior to BDP (P < 0.001). All treatments were well tolerated. CONCLUSION: Budesonide Turbuhaler (200 microg) was as effective as 400 microg BDP pMDI. The efficacy of budesonide was improved significantly by increasing the dosage to 800 microg daily. The study design shows the importance of including a higher dose treatment group when comparing two formulations of inhaled corticosteroids in order to determine whether the treatments to be compared are on the steep part of the dose-response curve. Without that information, comparative studies are usually inconclusive.


Assuntos
Anti-Inflamatórios/uso terapêutico , Asma/tratamento farmacológico , Beclometasona/uso terapêutico , Budesonida/uso terapêutico , Nebulizadores e Vaporizadores , Anti-Inflamatórios/efeitos adversos , Anti-Inflamatórios/farmacologia , Beclometasona/efeitos adversos , Beclometasona/farmacologia , Budesonida/efeitos adversos , Budesonida/farmacologia , Qualidade de Produtos para o Consumidor , Relação Dose-Resposta a Droga , Feminino , Volume Expiratório Forçado/efeitos dos fármacos , Humanos , Japão , Masculino , Pessoa de Meia-Idade , Pico do Fluxo Expiratório/efeitos dos fármacos , Estatísticas não Paramétricas
9.
Intern Med ; 40(1): 61-7, 2001 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-11201374

RESUMO

We report two cases of severe bronchopneumonia due to influenza A (H3N2) virus. The severity of the disease necessitated initiation of empiric therapy based on the present illness and clinical data on admission. Both patients were improved by artificial ventilation with positive end-expiratory pressures and administration of broad spectrum antibiotics and corticosteroids before confirming the diagnosis of viral bronchopneumonia using viral culture and serological tests. Within 24 hours, influenza A (H3N2) virus was identified by amplification of the pathogen genes by reverse transcription polymerase chain reaction (RT-PCR) using the stored bronchoalveolar lavage (BAL) fluids of both cases. This suggests that a combination of detection methods of pathogens using RT-PCR and BAL fluid will facilitate determination of rational treatment aimed at influenza A virus.


Assuntos
Broncopneumonia/etiologia , Vírus da Influenza A Subtipo H3N2 , Vírus da Influenza A/isolamento & purificação , Pneumonia Viral/etiologia , RNA Viral/análise , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Idoso , Antibioticoprofilaxia , Betametasona/uso terapêutico , Líquido da Lavagem Broncoalveolar/virologia , Broncopneumonia/terapia , Broncopneumonia/virologia , Cefalosporinas/uso terapêutico , Clindamicina/uso terapêutico , Terapia Combinada , Quimioterapia Combinada/uso terapêutico , Fosfomicina/uso terapêutico , Humanos , Vírus da Influenza A/genética , Masculino , Metilprednisolona/uso terapêutico , Pessoa de Meia-Idade , Minociclina/uso terapêutico , Pneumonia Viral/terapia , Pneumonia Viral/virologia , Respiração com Pressão Positiva , Respiração Artificial
10.
Respiration ; 68(1): 35-40, 2001.
Artigo em Inglês | MEDLINE | ID: mdl-11223728

RESUMO

BACKGROUND: The percentage of the aged among all patients with bronchial asthma is increasing. OBJECTIVE: To investigate the risk factors for the development of steroid-dependent asthma in the elderly. METHODS: A multiple logistic regression analysis involving various clinical factors between steroid-dependent and -independent asthma was carried out for 59 asthmatics aged over 60 years, including 16 patients with steroid-dependent asthma. The calculated risk for each factor was compared with that obtained from 122 younger asthmatics aged 20-59 years. RESULTS: Among the factors examined (sex, age, period from onset of asthma, type of asthma and family history of asthma, plus history of smoking, atopic dermatitis, allergic rhinitis, chronic sinusitis and nasal polyps), the significant risk factors for the development of steroid dependency in the elderly asthmatics were only family history of bronchial asthma (relative risk 3.6) and smoking history (relative risk 6.9). CONCLUSIONS: Some risk factors for steroid-dependent asthma in younger individuals were not significant in the elderly. Since the smoking history was most closely associated with the development of steroid dependency in the elderly, even though most of them had quit smoking, it is important for patients with asthma to avoid smoking.


Assuntos
Asma/tratamento farmacológico , Asma/epidemiologia , Esteroides/administração & dosagem , Adulto , Distribuição por Idade , Idoso , Idoso de 80 Anos ou mais , Asma/complicações , Dermatite/complicações , Feminino , Humanos , Incidência , Modelos Logísticos , Masculino , Pessoa de Meia-Idade , Análise Multivariada , Pólipos Nasais/complicações , Probabilidade , Valores de Referência , Testes de Função Respiratória , Fatores de Risco , Índice de Gravidade de Doença , Distribuição por Sexo , Sinusite/complicações , Fumar/efeitos adversos , Estatísticas não Paramétricas , Transtornos Relacionados ao Uso de Substâncias
12.
Nihon Kokyuki Gakkai Zasshi ; 39(10): 781-6, 2001 Oct.
Artigo em Japonês | MEDLINE | ID: mdl-11828735

RESUMO

A 78-year-old man was hospitalized on February 29, 2000 because of dyspnea. A chest radiograph showed diffuse bilateral interstitial shadows associated with pulmonary volume loss. We could not obtain histological evidence of idiopathic interstitial pneumonia (IIP) because of his advanced age and severe respiratory dysfunction. IIP was diagnosed on the basis of radiographic findings and clinical symptoms. The patient was intubated and mechanical ventilation was performed. After one course of pulsed cyclophosphamide (CPM) and methylprednisolone therapy, the hypoxemia improved and it became possible to wean the patient from the ventilator. After five courses of pulsed CPM therapy, the dose of oral corticosteroid was tapered. CPM was administered safely without any severe side effects. Pulsed CPM therapy appears to be a viable alternative method of treatment for IIP.


Assuntos
Anti-Inflamatórios/administração & dosagem , Ciclofosfamida/administração & dosagem , Doenças Pulmonares Intersticiais/tratamento farmacológico , Metilprednisolona/administração & dosagem , Idoso , Esquema de Medicação , Quimioterapia Combinada , Humanos , Masculino , Pulsoterapia
16.
Chest ; 118(4): 959-65, 2000 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-11035663

RESUMO

STUDY OBJECTIVE: To assess the uncovered Ultraflex nitinol stent (Boston Scientific; Natick, MA) for its efficacy and safety. DESIGN, SETTING, AND PATIENTS: Between October 1997 and October 1998, we carried out a prospective multicenter study at six hospitals in Japan. Fifty-four Ultraflex stents were inserted in 34 patients with inoperable malignant airway stenosis using a flexible and/or a rigid bronchoscope under fluoroscopic and endoscopic visualization. MEASUREMENTS AND RESULTS: Clinical, endoscopic examination, and pulmonary function on days 1, 30, and 60 after stent implantation showed improvement. In 19 patients (56%), stent implantation was performed as an emergency procedure because of life-threatening tracheobronchial obstruction. Immediate relief of dyspnea was achieved in 82% of the patients. The dyspnea index improved significantly after implantation (before vs. days 1, 30, and 60; p<0.001). Significant improvements were observed in obstruction of airway diameter (81+/-15% before vs. 14+/-17% on day 1, 12+/-12% on day 30, and 22+/-28% on day 60; p<0.001). Vital capacity (VC), FEV(1), and peak expiratory flow (PEF) increased significantly after stent implantation: before vs immediately after VC (p<0.01), FEV(1) (p<0.001), and PEF (p<0.05). The main complications were tumor ingrowth (24%) and tumor overgrowth (21%). After coagulation with an Nd-YAG laser or argon plasma coagulation, mechanical coring out using the bevel of a rigid bronchoscope was necessary in patients showing tumor ingrowth or overgrowth. Removal and reposition were possible in case of misplacement. There were no problems with migration and retained secretions. The median survival time of patients was 3 months. The 1-year survival rate was 25.4%. CONCLUSIONS: In this study of the Ultraflex nitinol stent, we have demonstrated that patients were relieved from dyspnea, which contributed to improved quality of life, with minimal complications. This stent can be used safely, even in the subglottic region. Owing to its excellent flexibility and biocompatibility, the stent is also indicated in certain complicated situations, eg, narrow stenosis, hourglass stenosis, curvilinear stenosis, bilateral mainstem bronchial stenoses, and long stenosis of varying diameters.


Assuntos
Ligas , Materiais Biocompatíveis , Neoplasias Pulmonares/complicações , Neoplasias do Mediastino/complicações , Implantação de Prótese/instrumentação , Stents , Estenose Traqueal/cirurgia , Adulto , Idoso , Idoso de 80 Anos ou mais , Broncoscopia , Carcinoma Broncogênico/complicações , Carcinoma Broncogênico/patologia , Carcinoma de Células Pequenas/complicações , Carcinoma de Células Pequenas/patologia , Feminino , Humanos , Neoplasias Pulmonares/patologia , Masculino , Neoplasias do Mediastino/patologia , Pessoa de Meia-Idade , Estadiamento de Neoplasias , Estudos Prospectivos , Desenho de Prótese , Testes de Função Respiratória , Segurança , Estenose Traqueal/etiologia , Estenose Traqueal/patologia , Estenose Traqueal/fisiopatologia
17.
Respirology ; 5(3): 231-40, 2000 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-11022985

RESUMO

OBJECTIVE: The aim of this study was to evaluate the oral steroid-sparing capacity of budesonide Turbuhaler. METHODOLOGY: One hundred and thirteen oral steroid-dependent patients were treated for 6 months with placebo or budesonide 800 microg or 1600 microg daily. Every second week the oral steroid dose was reduced if asthma control permitted. RESULTS: The reductions in oral steroid doses were 9, 35 and 60% in the placebo and budesonide 800 microg and 1600 microg groups, respectively. Oral steroid treatment could be discontinued in 4% (placebo), 15% (800 microg) and 23% (1600 microg). Mean peak expiratory flow values increased by 21 and 24 L/min in the budesonide groups but decreased by 6 L/min in the placebo group. Asthma attack, activity and sleep scores remained unchanged showing maintained efficacy. Plasma cortisol levels increased and an adrenocorticotropic hormone test showed improved adrenocortical response in both budesonide groups, indicating improved safety. Adverse drug reactions were infrequent and mild in all study groups. CONCLUSION: Budesonide Turbuhaler, 800 microg and 1600 microg daily, resulted in a significant reduction in oral steroid usage in steroid-dependent patients. The effect was achieved with maintained asthma control together with improvements in lung and adrenal functions.


Assuntos
Anti-Inflamatórios/administração & dosagem , Asma/tratamento farmacológico , Broncodilatadores/administração & dosagem , Budesonida/administração & dosagem , Glucocorticoides/administração & dosagem , Prednisolona/administração & dosagem , Administração por Inalação , Administração Oral , Adolescente , Hormônio Adrenocorticotrópico , Adulto , Anti-Inflamatórios/efeitos adversos , Asma/sangue , Asma/fisiopatologia , Broncodilatadores/efeitos adversos , Budesonida/efeitos adversos , Interpretação Estatística de Dados , Relação Dose-Resposta a Droga , Método Duplo-Cego , Quimioterapia Combinada , Feminino , Humanos , Hidrocortisona/sangue , Japão , Masculino , Pessoa de Meia-Idade , Nebulizadores e Vaporizadores , Pico do Fluxo Expiratório , Placebos , Estudos Prospectivos , Sono/efeitos dos fármacos
18.
Respirology ; 5(3): 247-56, 2000 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-11022987

RESUMO

OBJECTIVE: The aim of this study was to investigate the dose-response for inhaled budesonide via Turbuhaler in Japanese patients with mild to moderate asthma. METHODOLOGY: Inhaled budesonide 100 microg, 200 microg, 400 microg or placebo was administered twice daily via Turbuhaler for 6 weeks, to 267 adult Japanese patients (mean age 51 years) with mild-to-moderate, non-steroid-dependent bronchial asthma, in a double-blind, placebo-controlled, randomized, parallel group study. The patients had to be symptomatic for more than 3 days/week and have an average morning peak expiratory flow (PEF) 50-80% of predicted normal value. RESULTS: The response to budesonide was rapid, all treatments showing a significant improvement in morning PEF after 1 week (P<0.05). During week 6, mean improvements of 15, 45, 53 and 71 L/min were observed for the placebo, 200 microg, 400 microg and 800 microg budesonide groups, respectively. Compared with placebo all improvements in the budesonide groups were statistically significant and a significant dose-response was demonstrated (P<0.001). The difference between the 200 microg and 800 microg doses was significant. Also, for several secondary efficacy variables (e.g. evening PEF, symptom score, treatment score, daily activity score and sleep score) significant dose-responses were shown. Other variables included the investigators' assessments of improvement and usefulness. They also showed statistically significant dose-response relationships and confirmed the rapid onset of action. Budesonide was well tolerated at all tested doses, with a low incidence of adverse events, all of which were minor in severity. CONCLUSIONS: Budesonide Turbuhaler in the doses 100 microg to 400 microg twice daily was effective, well tolerated and showed a rapid onset of action in patients with mild-to-moderate asthma. Dose-response was demonstrated for several variables of clinical efficacy.


Assuntos
Anti-Inflamatórios/administração & dosagem , Asma/tratamento farmacológico , Broncodilatadores/administração & dosagem , Budesonida/administração & dosagem , Administração por Inalação , Anti-Inflamatórios/efeitos adversos , Asma/fisiopatologia , Broncodilatadores/efeitos adversos , Budesonida/efeitos adversos , Ritmo Circadiano , Relação Dose-Resposta a Droga , Método Duplo-Cego , Feminino , Volume Expiratório Forçado , Humanos , Japão , Masculino , Pessoa de Meia-Idade , Nebulizadores e Vaporizadores , Pico do Fluxo Expiratório , Placebos , Estudos Prospectivos , Resultado do Tratamento , Capacidade Vital
20.
Clin Nephrol ; 54(2): 147-50, 2000 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-10968692

RESUMO

AIM AND METHODS: To investigate the relationship between macrophage migration inhibitory factor and clinical or pathological findings in patients with myeloperoxidase anti-neutrophil cytoplasmic antibody MPO-ANCA-associated glomerulonephritis characterized by idiopathic necrotizing crescentic glomerulonephritis, renal biopsy specimens from 16 patients with MPO-ANCA-associated glomerulonephritis and 15 controls were stained using an enzyme antibody method to detect macrophage migration inhibitory factor and macrophages infiltrating the glomeruli. The relationship of this factor with various clinical parameters and with cellular crescents was determined. RESULTS: Macrophage migration inhibitory factor was detected in 11 out of 16 patients with MPO-ANCA-associated glomerulonephritis, but was not found in any of the controls. In the positive patients, the blood MPO-ANCA level was significantly higher than in the negative patients. Both cellular crescents and the number of macrophages infiltrating the glomeruli were significantly increased in the patients positive for macrophage migration inhibitory factor. CONCLUSION: Thus, macrophage migration inhibitory factor may be closely related to cellular crescent formation and disease activity in patients with MPO-ANCA-associated glomerulonephritis.


Assuntos
Anticorpos Anticitoplasma de Neutrófilos/imunologia , Glomerulonefrite/metabolismo , Fatores Inibidores da Migração de Macrófagos/metabolismo , Peroxidase/imunologia , Biópsia , Estudos de Casos e Controles , Feminino , Glomerulonefrite/imunologia , Glomerulonefrite/patologia , Humanos , Glomérulos Renais/patologia , Macrófagos/patologia , Masculino , Pessoa de Meia-Idade
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