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31.
Matsumoto A Tanaka E Morita S Yoshizawa K Umemura T Joshita S 《Journal of gastroenterology》2012,47(9):1006-1013
Background
Despite its status as a potential biomarker of hepatitis B virus (HBV) response to interferon treatment, the changes in hepatitis B surface antigen (HBsAg) levels over the natural course of HBV carriers have not been analyzed sufficiently.Methods
A total of 101 HBV carriers were followed prospectively from 1999 to 2009. HBsAg level was measured yearly during the followed period.Results
HBsAg levels at baseline ranged from ?1.4 to 5.32 log IU/ml, with a median value of 3.2 log IU/ml. Lower HBsAg levels were significantly associated with higher age and lower HBV replication status. The rate of change of HBsAg levels showed two peaks, with a cut-off value of ?0.4 log IU/year. Based on this, patients were tentatively classified into rapid decrease (rate of change 0.4 log IU/year) and non-rapid decrease groups. All baseline levels of HBsAg, HB core-related Ag, and HBV DNA were lower in the rapid decrease group than in the non-rapid decrease group. Patients with persistently positive HBeAg were all classified into the non-rapid decrease group. In patients with persistently negative HBeAg, HBV DNA levels were significantly (P?=?0.028) lower in the rapid decrease group than in the non-rapid decrease group.Conclusions
Lower baseline HBsAg levels were significantly associated with older age and lower viral activity. Both a loss of HBeAg detection as well as inactive replication of HBV are suggested to be fundamental factors contributing to a rapid decrease in HBsAg over the natural course of HBV infection. 相似文献32.
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36.
Taro Ohba Gouji Toyokawa Takuro Kometani Kaname Nosaki Fumihiko Hirai Masafumi Yamaguchi Motoharu Hamatake Takashi Seto Yukito Ichinose Kenji Sugio 《Surgery today》2014,44(3):478-486
Purpose
This study retrospectively assessed the mutations of the epidermal growth factor receptor (EGFR) and K-ras genes and their clinical significance in patients with resected stage I adenocarcinomas.Methods
A total of 354 patients with resected lung adenocarcinomas were included, and 256 patients with stage I disease were analyzed for the prognostic and predictive value of these mutations.Results
Mutations of EGFR and K-ras genes were detected in 149 (41.1 %) and 23 (6.4 %) of all tumors, and in 122 (47.6 %) and 14 (5.5 %) of stage I tumors, respectively. There were no significant differences in the disease-free survival (DFS) and overall survival (OS) between the EGFR-mutant and wild-type groups. However, the DFS and OS were significantly shorter in patients with K-ras mutations than in those without (5-year DFS: 50.8 vs. 76.9 %, 5-year OS: 70.0 vs. 86.6 %, p < 0.01). A multivariate analysis showed that K-ras mutations were an independent poor prognostic factor. Twenty-four of the 41 patients with recurrent disease after surgery were treated with an EGFR–TKI. Fifteen EGFR-mutant patients treated with an EGFR–TKI had a better prognosis than did the nine EGFR-wild-type patients.Conclusion
The presence of an EGFR gene mutation was a predictive factor for the response to EGFR–TKI treatment in patients with resected stage I adenocarcinoma, but was not a prognostic factor. The presence of a K-ras gene mutation was a poor prognostic factor. 相似文献37.
Toshihiro Sawai Masaomi Nangaku Akira Ashida Rika Fujimaru Hiroshi Hataya Yoshihiko Hidaka Shinya Kaname Hirokazu Okada Waichi Sato Takashi Yasuda Yoko Yoshida Yoshihiro Fujimura Motoshi Hattori Shoji Kagami 《Clinical and experimental nephrology》2014,18(1):4-9
Atypical hemolytic uremic syndrome (aHUS) is rare and comprises the triad of microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury. Recently, abnormalities in the mechanisms underlying complement regulation have been focused upon as causes of aHUS. The prognosis for patients who present with aHUS is very poor, with the first aHUS attack being associated with a mortality rate of ~25 %, and with ~50 % of cases resulting in end-stage renal disease requiring dialysis. If treatment is delayed, there is a high risk of this syndrome progressing to renal failure. Therefore, we have developed diagnostic criteria for aHUS to enable its early diagnosis and to facilitate the timely initiation of appropriate treatment. We hope these diagnostic criteria will be disseminated to as many clinicians as possible and that they will be used widely. 相似文献
38.
Osamu Uemura Takuhito Nagai Kenji Ishikura Shuichi Ito Hiroshi Hataya Yoshimitsu Gotoh Naoya Fujita Yuko Akioka Tetsuji Kaneko Masataka Honda 《Clinical and experimental nephrology》2014,18(5):718-725
Background
Renal inulin clearance is the gold standard for evaluation of kidney function, but is compromised by problems of collecting urine samples in children, especially those <6 years or with a bladder dysfunction. Therefore, we should utilize the serum cystatin C (cysC)-based estimated glomerular filtration rate (eGFR) for measuring serum cysC. The purpose of the present study is to determine the applicability of the new serum cysC-based eGFR in Japanese children and adolescents, including infants with chronic kidney disease (CKD), for evaluation of renal function.Methods
Inulin clearance and standardized serum cysC level determined by the colloidal gold immunoassay were measured in 135 pediatric CKD patients between the ages of 1 month and 18 years with no underlying disease that affects renal function except CKD, to determine serum cysC-based eGFR in Japanese children and adolescents.Results
We showed the inulin clearance by expression of 1/serum cysC in pediatric CKD patients, which resulted in the equation: inulin GFR (mL/min/1.73 m2) = 104.1 × 1/serum cysC (mg/L) ? 7.80. We also validated the cysC-based eGFR formula for Japanese adults. eGFR values obtained with the adult formula significantly underestimated GFR by approximately 8 % in children with CKD.Conclusion
We determined the new cysC-based eGFR formula is useful for clinical screening of renal function in Japanese children and adolescents, including infants. 相似文献39.
Kaname Okura Kazunari Miyazaki Hiroki Muroyama Toshiaki Matsui Koichi Eguchi 《RSC advances》2018,8(56):32102
Ammonia decomposition has attracted increasing attention as a promising process for the on-site generation of hydrogen. In this study, Ni catalysts supported on perovskite-type oxides (ABO3) were prepared and the activity for ammonia decomposition was examined. The Ni/ANbO3 (A = Na and K) and Ni/AEMnO3 (AE = Ca, Sr, and Ba) catalysts were less effective for this reaction. Meanwhile, the Ni/REAlO3 (RE = La, Sm, and Gd) catalysts exhibited relatively high activity. For Ni/AETiO3 and Ni/AEZrO3, the performance strongly depended on the A-site element of the perovskite-type oxides, and the Sr and Ba elements were more effective than the Ca one in the respective series. The catalytic activity for Ni/AEZrO3 was higher than Ni/AETiO3 in the case of the same alkaline earth element, and Ni/BaZrO3 was the most active among the samples investigated in this work. For these series, the order in the performance corresponded well with that in the basic property. The nitrogen desorption profiles revealed that the evolution of nitrogen atoms, which is one of the kinetically slow steps, effectively proceeded for Ni/SrZrO3 and Ni/BaZrO3 compared with the conventional Ni catalysts. This promotion effect would be ascribed to the strong basic properties of the SrZrO3 and BaZrO3 supports, resulting in the high activity of Ni/SrZrO3 and Ni/BaZrO3 for ammonia decomposition.Ni/SrZrO3 and Ni/BaZrO3 catalysts showed high activity for ammonia decomposition since these supports promoted the nitrogen desorption step. 相似文献
40.
Hereditary hemorrhagic telangiectasia with growing pulmonary arteriovenous fistulas followed for 24 years 总被引:1,自引:0,他引:1
M Teragaki K Akioka M Yasuda Y Ikuno H Oku K Takeuchi T Takeda 《The American journal of the medical sciences》1988,295(6):545-547
A 47-year-old man was admitted for follow-up of an abnormal chest x-ray. He had a history of epistaxis and a brain abscess and a family history of pulmonary arteriovenous fistulas. Physical examination showed clubbed fingers and telangiectasia of the tongue. Laboratory data revealed evidence of polycythemia and hypoxia. Contrast echocardiography and pulmonary perfusion scintigraphy were suggestive of a right-to-left shunt. From the oxygen tension and content of blood taken at cardiac catheterization, the shunt ratio was calculated to be 57.8%. Multiple bilateral pulmonary arteriovenous fistulas were confirmed by angiography, and the patient was diagnosed as having hereditary hemorrhagic telangiectasia. A review of x-ray films taken over a 24-year period demonstrated that the fistulas in both lungs had been increasing gradually in size at different rates. A right lower lobectomy relieved the hypoxia, but the patient died unexpectedly on the twelfth postoperative day. There was no evidence of fistula rupture on chest film, but no autopsy was performed. 相似文献