Naho Obayashi
Juntendo University
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Publication
Featured researches published by Naho Obayashi.
Helicobacter | 2016
Naho Obayashi; Yoshikazu Ohtsuka; Kenji Hosoi; Tamaki Ikuse; Keisuke Jimbo; Yo Aoyagi; Tohru Fujii; Takahiro Kudo; Daisuke Asaoka; Mariko Hojo; Akihito Nagahara; Sumio Watanabe; Toshiaki Shimizu
Although Helicobacter pylori infection among adults is a major risk factor for the development of gastric cancer and initial infection with H. pylori may occur before 5 years of age, the direct effects of H. pylori infection since childhood on gastric mucosa are unknown. The aim of this study was to evaluate gene expression in the H. pylori‐infected gastric mucosa of children.
Pediatrics International | 2012
Tamaki Ikuse; Yoshikazu Ohtsuka; Takahiro Kudo; Kenji Hosoi; Naho Obayashi; Keisuke Jimbo; Yo Aoyagi; Tohru Fujii; Satoru Nagata; Toshiaki Shimizu
Background: Although initial infection with Helicobacter pylori may occur before 5 years of age, the pediatric mucosal immune response against H. pylori is not clear. The aim of the present study was to evaluate immune responses in the H. pylori‐infected gastric mucosa of children using microarray and real‐time polymerase chain reaction (PCR) analysis of pediatric gastric samples.
Journal of Pediatric Gastroenterology and Nutrition | 2016
Naho Obayashi; Katsuhiro Arai; Natsuko Nakano; Tomoyuki Mizukami; Toshinao Kawai; S. Yamamoto; Hirotaka Shimizu; Hiroyuki Nunoi; Toshiaki Shimizu; Julian Tang; Masafumi Onodera
Background: Chronic granulomatous disease (CGD) is a rare inherited disorder in which phagocytes are unable to eradicate pathogens because of a deficit of nicotinamide adenine dinucleotide phosphate oxidase. Among CGD patients, ∼30% to 50% develop severe gastrointestinal tract symptoms. Although characteristic histologic findings of CGD-associated colitis have been reported, information on endoscopic features remained vague. Methods: A total of 8 male patients with CGD (ages 2–23 years) from 2 Japanese institutions underwent colonoscopy for the evaluation of their fever, diarrhea, bloody stool, and abdominal pain. The endoscopic and histologic findings were retrospectively reviewed. Results: The endoscopic findings of CGD-associated colitis appeared varied. Notably, brownish dots over a yellowish edematous mucosa were observed in 3 of the 8 patients. Prominent pigment-laden macrophages were noted histologically on the mucosa. Conclusions: Although nonspecific endoscopic findings of CGD-associated colitis have been reported before, our observation of brownish dots spread across a yellowish edematous mucosa, termed “leopard sign,” could be a unique feature of this condition.
Pediatrics International | 2015
Katsuhiro Arai; Rie Funayama; Mieko Takahashi; Rie Sakai; Hirotaka Shimizu; Naho Obayashi; Akira Matsui
Predictive equations are often used to estimate resting energy expenditure (REE). Determining the appropriate equation for different patient types, however, remains inconclusive, as in the case of Japanese children with Crohns disease (CD). The aim of this study was to identify an appropriate predictive equation for measuring REE in Japanese children with CD.
Pediatric Transplantation | 2014
Kei Minowa; Katsuhiro Arai; Mureo Kasahara; Seisuke Sakamoto; Hirotaka Shimizu; Natsuko Nakano; Reiko Ito; Naho Obayashi; Atsuko Nakazawa; Akira Ishiguro
Thrombocytopenia is a major risk factor for cirrhotic liver disease. Patients with thrombocytopenia may have esophageal or gastric varices secondary to portal hypertension, leading to variceal bleeding which exposes the liver to further damage. Here, we present a female pediatric patient with PSC and CD, whose progressive thrombocytopenia was successfully controlled by romiplostim, a TPO receptor agonist. The patient developed bloody diarrhea at four yr of age, and was subsequently diagnosed with PSC and CD when seven yr old. While CD was well‐controlled by immunomodulators, the patients thrombocytopenia gradually progressed resulting in petechiae (platelet count of 11 × 109/L) when she was 10 yr and four months old. She responded poorly to immunoglobulin and corticosteroids. Weekly subcutaneous injection of romiplostim was therefore initiated, and platelet counts were maintained over at 50 × 109/L. She was able to undergo successful LDLT without platelet transfusion seven months after the initiation of romiplostim. Romiplostim was not required after LDLT with improved platelet counts. This case report suggests that romiplostim may be effective in the treatment of thrombocytopenic children with liver cirrhosis and portal hypertension, and in eliminating the need for platelet transfusion during the peri‐transplant period.
Pediatrics International | 2018
Tamaki Ikuse; Yoshikazu Ohtsuka; Naho Obayashi; Keisuke Jimbo; Yo Aoyagi; Takahiro Kudo; Daisuke Asaoka; Mariko Hojo; Akihito Nagahara; Sumio Watanabe; Thomas G. Blanchard; Steven J. Czinn; Toshiaki Shimizu
Chronic Helicobacter pylori infection in children induces lymphoid hyperplasia called nodular gastritis (NG) at the antral gastric mucosa. The aim of this study was to evaluate genes in gastric biopsy on microarray analysis, to identify molecules associated with NG on comparison with NG‐negative pediatric corpus tissue and with H. pylori‐infected adult tissue with atrophic gastritis (AG).
Pediatrics International | 2015
Naho Obayashi; Mitsuyoshi Suzuki; Tomoaki Yokokura; Nakayuki Naritaka; Satoshi Nakano; Yoshikazu Ohtsuka; Hiroyuki Sugo; Seiji Kawasaki; Toshiaki Shimizu
Increasingly, food allergy associated with tacrolimus after pediatric living‐donor liver transplantation (LT) has been reported. Tacrolimus prevents the activation of T cells by blocking calcineurin, thus producing an immunosuppressive effect, but tacrolimus induces an imbalance in T‐helper type 1 (Th1) and Th2 cells in the food allergy process. This report describes a case of tacrolimus‐associated food allergy after pediatric living‐donor LT. The patient was a 7‐year‐old Japanese girl who had undergone living‐donor LT at 12 months of age, and whom we first saw in the clinic at age 18 months. She received immunosuppressive therapy by tacrolimus after transplantation. Atopic dermatitis developed in post‐transplant month 18. Stridor, facial edema, lip swelling, and skin erythema after consuming tempura udon containing wheat occurred in post‐transplant month 39, and she was subsequently diagnosed with anaphylactic shock. Eosinophilic leukocyte and serum immunoglobulin (Ig)E increased, and specific IgE was positive for some food allergens. Pharmacotherapy was therefore changed from tacrolimus to cyclosporine A, after which eosinophilic leukocyte and serum IgE decreased and atopic dermatitis improved.
Nihon Shoni Arerugi Gakkaishi. The Japanese Journal of Pediatric Allergy and Clinical Immunollogy | 2017
Takahiro Kudo; Itsuhiro Oka; Nobuyasu Arai; Reiko Kyodo; Masamichi Sato; Eri Miyata; Kenji Hosoi; Seiichi Matsumura; Naho Obayashi; Tamaki Ikuse; Keisuke Jimbo; Mari Mori; Yo Aoyagi; Tohru Fujii; Yoshikazu Ohtsuka; Toshiaki Shimizu
Ai Magazine | 2017
Tamaki Ikuse; Yo Aoyagi; Naho Obayashi; Keisuke Jimbo; Takahiro Kudo; Yoshikazu Ohtsuka; Thomas G. Blanchard; Steven J. Czinn; Toshiaki Shimizu
Ai Magazine | 2017
Tamaki Ikuse; Takahiro Kudo; Naho Obayashi; Keisuke Jimbo; Yo Aoyagi; Yoshikazu Ohtsuka; Thomas G. Blanchard; Steven J. Czinn; Toshiaki Shimizu