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Nobusuke Kimura Yukitoshi Takahashi Hideo Shigematsu Katsumi Imai Hiroko Ikeda Hideyuki Ootani Rumiko Takayama Yukiko Mogami Noriko Kimura Koichi Baba Kazumi Matsuda Takayasu Tottori Naotaka Usui Satohiko Kondou Yushi Inoue 《Brain & development》2019,41(1):77-84
Objective
The purpose of this study was to identify the risk factors of cognitive impairment in pediatric epilepsy patients with focal cortical dysplasia (FCD).Methods
77 patients with histopathologically confirmed FCD were studied. The statistical relationship between cognition levels and clinical factors at presurgical evaluation was analyzed. Cognitive function was evaluated by development quotient or intelligence quotient (DQ-IQ).Results
Ages at seizure onset were younger than 15?years (mean?±?SD; 5.0?±?4.2?years). Mean disease duration was 14.5?±?8.5?years. Mean age at pre-surgical DQ-IQ evaluation was 34.8?±?10.7?years. Mean DQ-IQ was 60.5?±?20.5, and 41 of 77 (53.2%) patients had mental retardation (DQ-IQ?<?70). Younger seizure onset and seizure clustering were significantly associated with lower DQ-IQ (p?<?0.001). A multiple regression study identified higher seizure frequency pattern, a history of epileptic spasm and status epilepticus as aggravating factors of DQ-IQ decline (R2?=?0.63, p?<?0.001). On the other hand, the risk was decreased in patients with habitual focal aware seizure and transient seizure-free periods up to 6?months in the course of epilepsy. FCD location (FCD site, extent of radiological lesion and laterality) and histopathology of FCD did not affect DQ-IQ.Conclusions
Our study suggests that seizure characteristics including higher seizure frequency pattern, a history of epileptic spasm, status epilepticus, seizure clustering and early onset of seizure are risk factors of cognitive impairment in FCD patients. 相似文献4.
5.
Jun Inoue Yukuto Sato Robert Sinclair Katsumi Tsukamoto Mutsumi Nishida 《Proceedings of the National Academy of Sciences of the United States of America》2015,112(48):14918-14923
Whole-genome duplication (WGD) is believed to be a significant source of major evolutionary innovation. Redundant genes resulting from WGD are thought to be lost or acquire new functions. However, the rates of gene loss and thus temporal process of genome reshaping after WGD remain unclear. The WGD shared by all teleost fish, one-half of all jawed vertebrates, was more recent than the two ancient WGDs that occurred before the origin of jawed vertebrates, and thus lends itself to analysis of gene loss and genome reshaping. Using a newly developed orthology identification pipeline, we inferred the post–teleost-specific WGD evolutionary histories of 6,892 protein-coding genes from nine phylogenetically representative teleost genomes on a time-calibrated tree. We found that rapid gene loss did occur in the first 60 My, with a loss of more than 70–80% of duplicated genes, and produced similar genomic gene arrangements within teleosts in that relatively short time. Mathematical modeling suggests that rapid gene loss occurred mainly by events involving simultaneous loss of multiple genes. We found that the subsequent 250 My were characterized by slow and steady loss of individual genes. Our pipeline also identified about 1,100 shared single-copy genes that are inferred to have become singletons before the divergence of clupeocephalan teleosts. Therefore, our comparative genome analysis suggests that rapid gene loss just after the WGD reshaped teleost genomes before the major divergence, and provides a useful set of marker genes for future phylogenetic analysis.The recent rapid growth of genome data has made it possible to clarify major evolutionary events that have shaped eukaryote genomes, such as gene duplication, chromosomal rearrangement, and whole-genome duplication (WGD) (1). In particular, WGD events, known to have occurred in several major lineages of flowering plants (2), budding yeasts (3), and vertebrates (4) (Fig. 1A), are considered to have had a major impact on genomic architecture and consequently organismal features.Open in a separate windowFig. 1.Inferred spatiotemporal process of gene loss and persistence after TGD in teleost ancestors. (A) The estimated numbers of gene loss events in the teleost phylogeny, time-scaled tree of vertebrates (11, 41) with the timing of genome duplication events at the base of vertebrates (VGD1/2) and teleosts (TGD), and the number of extant species (26). Species used in this study are connected by solid branches. The numbers were parsimoniously inferred from the presence or absence of TGD-derived gene lineage pairs belonging to 6,892 orthogroups and mapped onto the time points of TGD (306 Mya), nodes a–g (a: 245 Mya; b: 158; c: 120; d: 105; e: 41; f: 164; g: 86) (11), and h (74 Mya) (28). On the left side of the tree, ortholog arrangements are compared between representatives (connected by bold branches in the tree) by CIRCOS (circos.ca) using orthology information for 5,655 orthogroups belonging to the 1to1 category (Fig. S2). (B) Definition of terms relating to WGD events. An orthogroup is a monophyletic group containing WGD-derived paralogs (gene lineages) of all focal species (Sp1) and orthologs of their sister species (Sp2), ignoring lineage-specific gene duplications (GeneA-1′ and -1″) or gene loss (GeneA-1″). (C) Approximation of the pattern of the number of gene loss and persistence events associated with TGD. The estimated number of retained paired gene lineages at nodes a to h and current teleosts (Ca, Ze, Co, Ti, Pl, Me, St, Te, and Fu) were used to compare the fit of the one-phase [αe–2μt (14)] and two-phase models. (D) Region of C detailing the recent pattern of gene loss. The solid and dashed curves have been corrected upward to remove the bias expected to result from parsimony analysis. These approximations are effectively insensitive to fluctuations in the estimated numbers of gene lineage pairs and times for the TGD event and ancestral nodes (a to h) (SI Text). The evolutionary scenario is essentially unchanged if the number of gene lineage pairs estimated without the BS 70% criterion or the divergence times estimated by nuclear gene (28)/mitochondrial genome (42) data were used. Note that the two-phase model can be roughly approximated by a double-exponential curve.Duplicate genes generated by WGD are typically assumed to be redundant and therefore subsequently lost in a stochastic manner. Comparative genome studies have suggested that 90% of duplicate genes were rapidly lost (5) by a neutral process (6) after WGD in budding yeast, but 20–30% of them were retained in human (7) even after several hundred million years. However, few genome-wide studies have addressed the temporal pattern of gene loss or persistence after WGD with reference to a reliable timescale (but see refs. 6 and 8). Such examination is indispensable for understanding when duplicate genes were lost and, consequently, genome structures were reshaped, during vertebrate diversification after the WGD (Fig. 1).To examine the detailed process of duplicate gene loss after WGD, one needs to estimate the number (proportion) of remaining duplicates in extant and ancestral species. For this purpose, both (i) reliably time-calibrated phylogenetic trees of species and (ii) well-annotated genomes are required. These two requirements have been met for several vertebrate lineages, including some teleost fishes. Given this, the next step should be to accurately estimate orthology and paralogy relationships of all of the genes that experienced WGD. For the analysis of gene orthology and paralogy, a homology search- or synteny-based approach has usually been used (9). In addition to the homology search-based approach (e.g., COGs and OrthoDB), a phylogenetic tree-based approach has also been introduced (e.g., Ensembl and PhylomeDB) (9). Recent developments of tree search algorithms and increased computing power allow a sophisticated tree-based approach, comparing each gene tree with the species tree. Such an approach is indispensable for the effective analysis of gene orthology and paralogy across many species, providing us with a powerful opportunity to investigate genome evolution after WGD.Here, we aim to investigate the gene loss/persistence pattern using genome-wide data, focusing on what is known as the teleost genome duplication (TGD). TGD is estimated to have occurred in an ancestor of teleosts (Fig. 1A) but after the divergence of tetrapods and teleosts (10). Thus, it is a relatively recent WGD shared by a large vertebrate group, i.e., the Teleostei. For teleosts, reliably time-calibrated phylogenies, including phylogenetic position and timing of the TGD event, are available (e.g., ref. 11). In addition, well-annotated whole-genome data from at least nine phylogenetically representative teleost species (cave fish, zebrafish, cod, tilapia, platyfish, medaka, stickleback, Tetraodon, and fugu) are now available from Ensembl (12). In the present study, we inferred the timing of rapid genome reshaping through gene loss after TGD by estimating the temporal and genomic positional (spatiotemporal) loss/persistence pattern of TGD-derived gene lineage pairs (Fig. 1B) over the past several hundred million years, using accurate tree-based orthology estimation (Fig. S1) and a reliable time-calibrated teleost tree. We investigated the mechanism of rapid gene loss after TGD by fitting a newly developed model for the observed temporal pattern of gene loss. This new model is necessary because standard models, based upon random and independent loss of duplicate genes, fail to fit our data. Our model analysis explicitly includes both the possibility of the loss of multiple genes in single events, and also the known phylogeny of the relevant species. The significance of the inclusion of events that result in the loss of multiple genes is that it reproduces the two phases of loss. The inclusion of known phylogeny allows us to correct for the bias associated with parsimony analysis. 相似文献
6.
Tomoro Hishiki Hiroshi Horie Yasuyuki Higashimoto Katsumi Yotsumoto Shugo Komatsu Yuri Okimoto Harumi Kakuda Yuichi Taneyama Takeshi Saito Keita Terui Tetsuya Mitsunaga Mitsuyuki Nakata Hidemasa Ochiai Moeko Hino Kumiko Ando Hideo Yoshida Jun Iwai 《Pediatric surgery international》2014,30(9):919-926
Purpose
In the recent years in Japan, an increasing number of patients with neuroblastoma (NB) are being treated by the “delayed local treatment (DL)” policy, undergoing surgery after the completion of high-dose chemotherapy with hematopoietic stem cell rescue (HDC). We reviewed the histopathological findings of second-look operations, including those of patients treated with DL.Patients
From 1998 to 2013, 26 patients with high-risk NB underwent radical operation following chemotherapy. Surgery was performed after induction chemotherapy in 17 cases (standard; STD), whereas 9 cases completed induction chemotherapy and HDC before undergoing tumor resection (DL). The amount of necrosis and the degree of differentiation within the post-treatment tumor were assessed.Results
Eighty-eight percent of the tumors showed necrosis in more than 1/3 of the specimen. Two DL cases showed complete disappearance of viable tumor cells. Amount of necrosis did not affect the prognosis of the patient. Tumors with immature, poorly differentiated phenotypes showed an extremely aggressive thereafter. Though not statistically proven, 123I-MIBG (metaiodobenzylguanidine) uptake may be correlated with the amount of viable cells remaining within the tumor, but not with the degree of differentiation.Conclusions
Our results support the previous reports advocating that tumors that sustain unfavorable histology after chemotherapy behave aggressively thereafter. 相似文献7.
Yamanaka K Nakagaki H Morita I Maeda N Ohara H Tomatsu S Nakashima T Watanabe Y Ohta N Shibata K 《Community dental health》2005,22(1):19-24
OBJECTIVE: To clarify the relationship between Candida carriage and drugs which have reported xerostomic side effects in the elderly. DESIGN: Cross-sectional study. Setting Two long-term care facilities in Aichi Pref., Japan. PARTICIPANTS: Eight men and 63 women with a mean age of 86 years (range 62 to 95 years) with at least some of their natural teeth. METHOD: Oral examination by dentists, microbiological test by microbiologists, questionnaire interviews, and data obtained from medical files. The Candida species (CFU) was adopted as an objective variable with risk indicators being age, number of teeth, saliva flow rate, denture wearing, xerostomic drugs, activities of daily living (ADL), frequency of brushing and type of meals. RESULTS: Bivariate analysis confirmed that participants with a higher number of Candida species (CFU) fell into the following categories: denture wearing (p < 0.05), older age (p < 0.05), xerostomic drugs (p < 0.10), more teeth, poor ADL, soft/liquid meals, and brushing once a day. This was in contrast to the categories of no denture wearing, younger age, no xerostomic drugs, fewer teeth, good ADL, normal meals, and brushing two or more times a day, in that order of significant probability on an ascending scale. A multiple logistics regression model confirmed that the variables of older age (80 years and over) and more teeth (six or more) had statistically significant (p < 0.05) effects on the number of Candida species present (CFU). Xerostomic drugs and the other variables had no significant effect. CONCLUSION: Older age and more teeth had a significant effect on the number of oral Candida species in the elderly. The results of this study did not support a role of those drugs as a risk indicator for oral Candida carriage. Larger trials are needed to assess the effect of drugs on the presence of oral Candida. 相似文献
8.
Nakashima M Yano H Akita S Tokunaga K Anraku K Tanaka K Hirano A 《The Journal of craniofacial surgery》2007,18(6):1466-1470
Forward dislocation of the temporomandibular joint commonly can be easily diagnosed and successfully reduced by manual repositioning. In this report, we discuss a rare case of prolonged temporomandibular dislocation that had persisted for more than 20 years because the otolaryngologist and dentist had missed the dislocation. This patient underwent open reduction and mandibular joint plasty with preoperative orthodontic therapy. It is possible that strong pain and mouth-closing disability may gradually remit and only deviated mandibular prognathism like malocclusion may persist. Therefore, abnormal occlusion warrants careful attention to temporomandibular joint dislocation. 相似文献
9.
Yamada K Hoshina H Arashiyama T Arasawa M Arai Y Uoshima K Tanaka M Nomura S 《Journal of prosthodontic research》2011,55(4):262-265
Purpose
The aim of this study was to develop and apply a new method for easy intraoperative adjustment of a provisional fixed full-arch restoration, in order to allow immediate implant loading following computer-guided surgery, regardless of any implant positioning errors compared to the virtual planning.Methods
In accordance with the NobelGuide™ protocol, a provisional restoration for immediate loading of six maxillary implants was prepared prior to surgery. Because small shifts between the planned and the actual implant positions were to be expected, the provisional restoration was not fabricated directly on temporary cylinders as a conventional one-piece superstructure, but was divided into two portions: six custom made abutments and a long span fixed restoration which were left unconnected. After implantation, the custom abutments were attached to the six implants to be immediately loaded, and the superstructure was cemented simultaneously to all abutments using dual cure resin cement. After the excess cement was cleaned and polished, the superstructure was then reseated. Passive fit was achieved between implants and the superstructure.Conclusion
The superstructure described in this article can be easily seated and adjusted to accommodate any possible shifts in implant positioning occurring during computer-guided surgery. Through this method uneventful immediate implant loading can be achieved in a reasonable operative time. 相似文献10.
Daisuke Gotoh MD PhD Nobutaka Shimizu MD PhD Naoki Wada MD PhD Katsumi Kadekawa MD PhD Tetsuichi Saito MD Shinsuke Mizoguchi MD PhD Yosuke Morizawa MD PhD Shunta Hori MD PhD Makito Miyake MD PhD Kazumasa Torimoto MD PhD William C. de Groat PhD Kiyohide Fujimoto MD PhD Naoki Yoshimura MD PhD 《Neurourology and urodynamics》2020,39(8):2120-2127