LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 10 of total 65

Search options

  1. Article ; Online: Effectiveness of drug safety measures for reducing the incidence of adverse drug reactions: Post-hoc analysis of data from all-case surveillance of iguratimod using generalized estimating equations.

    Shibata, Kai / Yoshimura, Akiko / Ikeuchi, Satoshi / Ishii, Mika

    PloS one

    2021  Volume 16, Issue 7, Page(s) e0253513

    Abstract: A post-marketing study was performed on all patients who had started treatment with iguratimod, a conventional synthetic disease-modifying antirheumatic drug approved in Japan. During the study period, various safety measures were implemented to reduce ... ...

    Abstract A post-marketing study was performed on all patients who had started treatment with iguratimod, a conventional synthetic disease-modifying antirheumatic drug approved in Japan. During the study period, various safety measures were implemented to reduce risks. We investigated the frequency of adverse drug reactions before and after implementation of each safety measure to examine the preventive effect of these measures. Post-hoc analysis was performed using data from all-case surveillance of iguratimod. The subjects were all of the patients receiving iguratimod for whom safety information was obtained. To identify the time after starting administration when adverse drug reactions were most likely to occur, a generalized linear mixed-effect model was applied for the period from initiation of administration until occurrence of reactions in each patient. The mean incidence of adverse drug reactions per patient was compared before and after the implementation of safety measures by using generalized estimating equations based on a two-sided test, 95% confidence interval, and 5% significance level. The number of patients treated with iguratimod was not related to changes in the number of patients with adverse drug reactions. After implementing precautions regarding co-administration with warfarin and liver dysfunction, the estimated mean incidence rate of adverse drug reactions (95% confidence interval) decreased significantly to 0.73 (0.59-0.90) and 0.72 (0.55-0.94), respectively. Accordingly, some of the implementation of safety measures significantly reduced adverse drug reactions. The effectiveness of safety measures implemented during the all-case surveillance of iguratimod was evaluated, revealing that early implementation of safety measures decreased the incidence of adverse drug reactions.
    MeSH term(s) Arthritis, Rheumatoid/drug therapy ; Arthritis, Rheumatoid/epidemiology ; Chromones/administration & dosage ; Chromones/adverse effects ; Humans ; Incidence ; Japan/epidemiology ; Male ; Middle Aged ; Models, Biological ; Product Surveillance, Postmarketing ; Prospective Studies ; Sulfonamides/administration & dosage ; Sulfonamides/adverse effects
    Chemical Substances Chromones ; Sulfonamides ; iguratimod (4IHY34Y2NV)
    Language English
    Publishing date 2021-07-30
    Publishing country United States
    Document type Clinical Trial ; Journal Article ; Multicenter Study ; Observational Study ; Research Support, Non-U.S. Gov't
    ISSN 1932-6203
    ISSN (online) 1932-6203
    DOI 10.1371/journal.pone.0253513
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: A novel homozygous HPDL variant in Japanese siblings with autosomal recessive hereditary spastic paraplegia: case report and literature review.

    Kojima, Fumikazu / Okamoto, Yuji / Ando, Masahiro / Higuchi, Yujiro / Hobara, Takahiro / Yuan, Junhui / Yoshimura, Akiko / Hashiguchi, Akihiro / Matsuura, Eiji / Takashima, Hiroshi

    Neurogenetics

    2024  Volume 25, Issue 2, Page(s) 149–156

    Abstract: Biallelic variants of 4-hydroxyphenylpyruvate dioxygenase-like (HPDL) gene have been linked to neurodegenerative disorders ranging from severe neonatal encephalopathy to early-onset spastic paraplegia. We identified a novel homozygous variant, c.340G > T ...

    Abstract Biallelic variants of 4-hydroxyphenylpyruvate dioxygenase-like (HPDL) gene have been linked to neurodegenerative disorders ranging from severe neonatal encephalopathy to early-onset spastic paraplegia. We identified a novel homozygous variant, c.340G > T (p.Gly114Cys), in the HPDL gene in two siblings with autosomal recessive hereditary spastic paraplegia (HSP). Despite sharing the same likely pathogenic variant, the older sister had pure HSP, whereas her brother had severe and complicated HSP, accompanied by early-onset mental retardation and abnormalities in magnetic resonance imaging. Given the clinical heterogeneity and potential for treatable conditions in HPDL-related diseases, we emphasize the importance of genetic testing for the HPDL gene.
    MeSH term(s) Humans ; Spastic Paraplegia, Hereditary/genetics ; Female ; Siblings ; Male ; Homozygote ; Pedigree ; Japan ; Child ; Magnetic Resonance Imaging ; Mutation/genetics ; East Asian People
    Language English
    Publishing date 2024-01-29
    Publishing country United States
    Document type Case Reports ; Journal Article ; Review ; Research Support, Non-U.S. Gov't
    ZDB-ID 1339887-8
    ISSN 1364-6753 ; 1364-6745
    ISSN (online) 1364-6753
    ISSN 1364-6745
    DOI 10.1007/s10048-024-00746-y
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article: Gene panel analysis of 119 index patients with suspected periodic paralysis in Japan.

    Yuan, Jun-Hui / Higuchi, Yujiro / Hashiguchi, Akihiro / Ando, Masahiro / Yoshimura, Akiko / Nakamura, Tomonori / Hiramatsu, Yu / Sakiyama, Yusuke / Takashima, Hiroshi

    Frontiers in neurology

    2023  Volume 14, Page(s) 1078195

    Abstract: Introduction: Genetic factors are recognized as the major reason for patients with periodic paralysis. The goal of this study was to determine the genetic causes of periodic paralysis in Japan.: Methods: We obtained a Japanese nationwide case series ... ...

    Abstract Introduction: Genetic factors are recognized as the major reason for patients with periodic paralysis. The goal of this study was to determine the genetic causes of periodic paralysis in Japan.
    Methods: We obtained a Japanese nationwide case series of 119 index patients (108 men and 11 women) clinically suspected of periodic paralysis, and a gene panel analysis, targeting
    Results: From 34 cases, 25 pathogenic/likely pathogenic/unknown significance variants were detected in
    Discussion: The low molecular diagnostic rate and specific genetic proportion of the present study highlight the etiological complexity of patients with periodic paralysis in Japan.
    Language English
    Publishing date 2023-01-26
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2564214-5
    ISSN 1664-2295
    ISSN 1664-2295
    DOI 10.3389/fneur.2023.1078195
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  4. Article ; Online: Geographic characteristics of HTLV-1 molecular subgroups and genetic substitutions in East Asia: Insights from complete genome sequencing of HTLV-1 strains isolated in Taiwan and Japan.

    Nozuma, Satoshi / Yoshimura, Akiko / Pai, Shun-Chung / Chen, Hung-Jen / Matsuura, Eiji / Tanaka, Masakazu / Kodama, Daisuke / Dozono, Mika / Matsuzaki, Toshio / Takashima, Hiroshi / Yang, Ya-Chien / Kubota, Ryuji

    PLoS neglected tropical diseases

    2024  Volume 18, Issue 2, Page(s) e0011928

    Abstract: Background: Although Japan is a major endemic area for human T-lymphotropic virus type 1 (HTLV-1) and the virus has been well-studied in this region, there is limited research on HTLV-1 in surrounding regions. In this study, we determined the complete ... ...

    Abstract Background: Although Japan is a major endemic area for human T-lymphotropic virus type 1 (HTLV-1) and the virus has been well-studied in this region, there is limited research on HTLV-1 in surrounding regions. In this study, we determined the complete genome sequences of HTLV-1 strains isolated from Taiwan and Japan and investigated the geographic characteristics of molecular subgroups and substitution mutations to understand the spread of HTLV-1 and its correlation with human migration.
    Methodology/principal findings: The complete genome sequences of 26 HTLV-1 isolates from Taiwan were determined using next-generation sequencing and were compared with those of 211 isolates from Japan in terms of subgroup and genetic mutations. In total, 15/26 (58%) isolates from Taiwan belonged to the transcontinental subgroup and 11/26 (42%) isolates belonged to the Japanese subgroup. The transcontinental subgroup was significantly more prevalent among Taiwanese isolates than Japanese isolates (58% vs 18%, P < 0.0001). The mutation rate for the complete HTLV-1 sequence was as low as 0.2%. On examining individual base substitutions, the G-to-A mutation was predominant. Bayesian phylogenetic tree analysis estimated the time to the most recent common ancestor for the transcontinental and Japanese subgroups to be 28447 years. The transcontinental subgroups from Taiwan and Japan appeared to form clusters according to their respective regions.
    Conclusions/significance: The transcontinental subgroup of HTLV-1 is predominant in Taiwan, while the Japanese subgroup is common in Japan. The difference in subgroup distribution may be attributed to the initial spread of the transcontinental subgroup in East Asia, followed by the influx of the Japanese subgroup.
    MeSH term(s) Humans ; Human T-lymphotropic virus 1 ; Japan/epidemiology ; HTLV-I Infections/epidemiology ; Taiwan/epidemiology ; Phylogeny ; Bayes Theorem ; Sequence Analysis, DNA ; Asia, Eastern/epidemiology ; Whole Genome Sequencing
    Language English
    Publishing date 2024-02-05
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2429704-5
    ISSN 1935-2735 ; 1935-2735
    ISSN (online) 1935-2735
    ISSN 1935-2735
    DOI 10.1371/journal.pntd.0011928
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  5. Article ; Online: A case of adult-onset Wolfram syndrome with compound heterozygous mutations of the WFS1 gene.

    Lee, Jinhee / Iwasaki, Takuya / Kaida, Tomoko / Chuman, Hideki / Yoshimura, Akiko / Okamoto, Yuji / Takashima, Hiroshi / Miyata, Kazunori

    American journal of ophthalmology case reports

    2022  Volume 25, Page(s) 101315

    Abstract: Purpose: Wolfram syndrome is a rare genetic disorder characterized by juvenile onset of diabetes mellitus with bilateral optic atrophy. We report a case of adult onset Wolfram syndrome with diabetes mellitus at age 22 and optic atrophy after age 40. The ...

    Abstract Purpose: Wolfram syndrome is a rare genetic disorder characterized by juvenile onset of diabetes mellitus with bilateral optic atrophy. We report a case of adult onset Wolfram syndrome with diabetes mellitus at age 22 and optic atrophy after age 40. The WFS1 gene sequence was analyzed in the patient and her father.
    Observations: A 46-year-old woman presented with bilateral vision loss. She had developed diabetes mellitus at age 22 and underwent bilateral cataract surgery at age 37. Visual acuity was 20/50 in the right eye and 20/200 in the left eye. The pupillary light reflex was sluggish in both eyes. Fundus examination showed bilateral optic atrophy, but there was no diabetic retinopathy. Cecocentral scotoma of both eyes was observed in Goldmann perimetry. There were no intracranial lesions on magnetic resonance imaging. Audiometry demonstrated high-frequency sensorineural hearing loss. Sequence analysis of the WFS1 gene revealed compound heterozygous mutation: c.908T>C p.L303P and c.1232_1233del, p.S411Cfs*131 in the patient and heterozygous mutation c. 908 T>C, p. L303P in her father.
    Conclusions and importance: The patient was diagnosed with adult-onset Wolfram syndrome with compound heterozygous mutations of the WFS1 alleles. Wolfram syndrome must be ruled out even in adult-onset diabetic patients with optic atrophy.
    Language English
    Publishing date 2022-01-22
    Publishing country United States
    Document type Case Reports
    ISSN 2451-9936
    ISSN (online) 2451-9936
    DOI 10.1016/j.ajoc.2022.101315
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  6. Article ; Online: Genetic spectrum and founder effect of non-dystrophic myotonia: a Japanese case series study.

    Yuan, Jun-Hui / Higuchi, Yujiro / Hashiguchi, Akihiro / Ando, Masahiro / Yoshimura, Akiko / Nakamura, Tomonori / Sakiyama, Yusuke / Takashima, Hiroshi

    Journal of neurology

    2022  Volume 269, Issue 12, Page(s) 6406–6415

    Abstract: Non-dystrophic myotonias (NDM) are rare skeletal muscle channelopathies, mainly linked to two voltage-gated ion channel genes, CLCN1 and SCN4A. The aim of this study is to identify the clinical and genetic features of patients with NDM in Japan. We ... ...

    Abstract Non-dystrophic myotonias (NDM) are rare skeletal muscle channelopathies, mainly linked to two voltage-gated ion channel genes, CLCN1 and SCN4A. The aim of this study is to identify the clinical and genetic features of patients with NDM in Japan. We collected a Japanese nationwide case series of patients with clinical diagnosis of NDM (1999-2021). Among 71 out of 88 pedigrees, using Sanger and next-generation sequencing targeting both CLCN1 and SCN4A genes, variants classified as pathogenic/likely pathogenic/unknown significance were detected from CLCN1 (31 probands), SCN4A (36 probands), or both genes (4 probands), and 11 of them were novel. Pedigrees carrying mono-allelic CLCN1 variants were more commonly seen than that with bi-allelic/double variants (24:7). Compared to patients with CLCN1 variants, patients harboring SCN4A variants showed younger onset age (5.64 ± 4.70 years vs. 9.23 ± 5.21 years), fewer warm-up phenomenon, but more paramyotonia, hyperCKemia, transient muscle weakness, and cold-induced myotonia. Haplotype analysis verified founder effects of the hot spot variants in both CLCN1 (p.T539A) and SCN4A (p.T1313M). This study reveals variants in CLCN1 and SCN4A from 80.7% of our case series, extending genetic spectrum of NDM, and would further our understanding of clinical similarity/diversity between CLCN1- and SCN4A-related NDM, as well as the genetic racial differences.
    MeSH term(s) Humans ; Infant ; Child, Preschool ; Child ; Myotonia/genetics ; Founder Effect ; NAV1.4 Voltage-Gated Sodium Channel/genetics ; Japan ; Chloride Channels/genetics ; Mutation/genetics ; Myotonia Congenita/genetics
    Chemical Substances NAV1.4 Voltage-Gated Sodium Channel ; Chloride Channels ; SCN4A protein, human
    Language English
    Publishing date 2022-07-30
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 187050-6
    ISSN 1432-1459 ; 0340-5354 ; 0012-1037 ; 0939-1517 ; 1619-800X
    ISSN (online) 1432-1459
    ISSN 0340-5354 ; 0012-1037 ; 0939-1517 ; 1619-800X
    DOI 10.1007/s00415-022-11305-6
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  7. Article ; Online: Investigation of the predictors of the response to Iguratimod therapy: A

    Ishiguro, Naoki / Shibata, Kai / Yoshimura, Akiko / Ikeuchi, Satoshi / Ishii, Mika

    Modern rheumatology

    2019  Volume 30, Issue 4, Page(s) 626–632

    Abstract: Objectives: ...

    Abstract Objectives:
    MeSH term(s) Adult ; Antirheumatic Agents/administration & dosage ; Antirheumatic Agents/therapeutic use ; Arthritis, Rheumatoid/drug therapy ; Chromones/administration & dosage ; Chromones/therapeutic use ; Drug Therapy, Combination ; Female ; Humans ; Male ; Methotrexate/administration & dosage ; Methotrexate/therapeutic use ; Middle Aged ; Product Surveillance, Postmarketing ; Sulfonamides/administration & dosage ; Sulfonamides/therapeutic use
    Chemical Substances Antirheumatic Agents ; Chromones ; Sulfonamides ; iguratimod (4IHY34Y2NV) ; Methotrexate (YL5FZ2Y5U1)
    Language English
    Publishing date 2019-08-08
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2078157-X
    ISSN 1439-7609 ; 1439-7595
    ISSN (online) 1439-7609
    ISSN 1439-7595
    DOI 10.1080/14397595.2019.1649110
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  8. Article ; Online: Factors influencing physician decisions to discontinue treatment after onset of liver dysfunction:

    Ishiguro, Naoki / Shibata, Kai / Yoshimura, Akiko / Ikeuchi, Satoshi / Ishii, Mika

    Modern rheumatology

    2019  Volume 30, Issue 4, Page(s) 633–639

    Abstract: Objectives: ...

    Abstract Objectives:
    MeSH term(s) Adult ; Antirheumatic Agents/administration & dosage ; Antirheumatic Agents/adverse effects ; Antirheumatic Agents/therapeutic use ; Arthritis, Rheumatoid/drug therapy ; Chemical and Drug Induced Liver Injury/epidemiology ; Chemical and Drug Induced Liver Injury/etiology ; Chromones/administration & dosage ; Chromones/adverse effects ; Chromones/therapeutic use ; Clinical Decision-Making ; Drug Therapy, Combination ; Female ; Humans ; Male ; Methotrexate/administration & dosage ; Methotrexate/therapeutic use ; Middle Aged ; Product Surveillance, Postmarketing ; Sulfonamides/administration & dosage ; Sulfonamides/adverse effects ; Sulfonamides/therapeutic use ; Treatment Outcome
    Chemical Substances Antirheumatic Agents ; Chromones ; Sulfonamides ; iguratimod (4IHY34Y2NV) ; Methotrexate (YL5FZ2Y5U1)
    Language English
    Publishing date 2019-08-12
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2078157-X
    ISSN 1439-7609 ; 1439-7595
    ISSN (online) 1439-7609
    ISSN 1439-7595
    DOI 10.1080/14397595.2019.1649229
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  9. Article ; Online: Identification and tracking of HTLV-1-infected T cell clones in virus-associated neurologic disease.

    Nozuma, Satoshi / Matsuura, Eiji / Tanaka, Masakazu / Kodama, Daisuke / Matsuzaki, Toshio / Yoshimura, Akiko / Sakiyama, Yusuke / Nakahata, Shingo / Morishita, Kazuhiro / Enose-Akahata, Yoshimi / Jacoboson, Steven / Kubota, Ryuji / Takashima, Hiroshi

    JCI insight

    2023  Volume 8, Issue 7

    Abstract: Human T lymphotropic virus type 1-assoicated (HTLV-1-associated) myelopathy/tropical spastic paraparesis (HAM/TSP) is a neuroinflammatory disease caused by the persistent proliferation of HTLV-1-infected T cells. Here, we performed a T cell receptor (TCR) ...

    Abstract Human T lymphotropic virus type 1-assoicated (HTLV-1-associated) myelopathy/tropical spastic paraparesis (HAM/TSP) is a neuroinflammatory disease caused by the persistent proliferation of HTLV-1-infected T cells. Here, we performed a T cell receptor (TCR) repertoire analysis focused on HTLV-1-infected cells to identify and track the infected T cell clones that are preserved in patients with HAM/TSP and migrate to the CNS. TCRβ repertoire analysis revealed higher clonal expansion in HTLV-1-infected cells compared with noninfected cells from patients with HAM/TSP and asymptomatic carriers (ACs). TCR clonality in HTLV-1-infected cells was similar in patients with HAM/TSP and ACs. Longitudinal analysis showed that the TCR repertoire signature in HTLV-1-infected cells remained stable, and highly expanded infected clones were preserved within each patient with HAM/TSP over years. Expanded HTLV-1-infected clones revealed different distributions between cerebrospinal fluid (CSF) and peripheral blood and were enriched in the CSF of patients with HAM/TSP. Cluster analysis showed similarity in TCRβ sequences in HTLV-1-infected cells, suggesting that they proliferate after common antigen stimulation. Our results indicate that exploring TCR repertoires of HTLV-1-infected cells can elucidate individual clonal dynamics and identify potential pathogenic clones expanded in the CNS.
    MeSH term(s) Humans ; Human T-lymphotropic virus 1 ; T-Lymphocytes ; Paraparesis, Tropical Spastic ; Clone Cells ; Receptors, Antigen, T-Cell
    Chemical Substances Receptors, Antigen, T-Cell
    Language English
    Publishing date 2023-04-10
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 2379-3708
    ISSN (online) 2379-3708
    DOI 10.1172/jci.insight.167422
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  10. Article ; Online: Dystonia and Parkinsonism in COA7-related disorders: expanding the phenotypic spectrum.

    Higuchi, Yujiro / Ando, Masahiro / Kojima, Fumikazu / Yuan, Junhui / Hashiguchi, Akihiro / Yoshimura, Akiko / Hiramatsu, Yu / Nozuma, Satoshi / Fukumura, Shinobu / Yahikozawa, Hiroyuki / Abe, Erika / Toyoshima, Itaru / Sugawara, Masashiro / Okamoto, Yuji / Matsuura, Eiji / Takashima, Hiroshi

    Journal of neurology

    2023  Volume 271, Issue 1, Page(s) 419–430

    Abstract: Background and objective: Biallelic mutations in the COA7 gene have been associated with spinocerebellar ataxia with axonal neuropathy type 3 (SCAN3), and a notable clinical diversity has been observed. We aim to identify the genetic and phenotypic ... ...

    Abstract Background and objective: Biallelic mutations in the COA7 gene have been associated with spinocerebellar ataxia with axonal neuropathy type 3 (SCAN3), and a notable clinical diversity has been observed. We aim to identify the genetic and phenotypic spectrum of COA7-related disorders.
    Methods: We conducted comprehensive genetic analyses on the COA7 gene within a large group of Japanese patients clinically diagnosed with inherited peripheral neuropathy or cerebellar ataxia.
    Results: In addition to our original report, which involved four patients until 2018, we identified biallelic variants of the COA7 gene in another three unrelated patients, and the variants were c.17A > G (p.D6G), c.115C > T (p.R39W), and c.449G > A (p.C150Y; novel). Patient 1 presented with an infantile-onset generalized dystonia without cerebellar ataxia. Despite experiencing an initial transient positive response to levodopa and deep brain stimulation, he became bedridden by the age of 19. Patient 2 presented with cerebellar ataxia, neuropathy, as well as parkinsonism, and showed a slight improvement upon levodopa administration. Dopamine transporter SPECT showed decreased uptake in the bilateral putamen in both patients. Patient 3 exhibited severe muscle weakness, respiratory failure, and feeding difficulties. A haplotype analysis of the mutation hotspot in Japan, c.17A > G (p.D6G), uncovered a common haplotype block.
    Conclusion: COA7-related disorders typically encompass a spectrum of conditions characterized by a variety of major (cerebellar ataxia and axonal polyneuropathy) and minor (leukoencephalopathy, dystonia, and parkinsonism) symptoms, but may also display a dystonia-predominant phenotype. We propose that COA7 should be considered as a new causative gene for infancy-onset generalized dystonia, and COA7 gene screening is recommended for patients with unexplained dysfunctions of the central and peripheral nervous systems.
    MeSH term(s) Humans ; Male ; Cerebellar Ataxia/genetics ; Dystonia ; Dystonic Disorders/complications ; Dystonic Disorders/diagnostic imaging ; Dystonic Disorders/genetics ; Levodopa ; Mutation/genetics ; Parkinsonian Disorders/complications ; Parkinsonian Disorders/diagnostic imaging ; Parkinsonian Disorders/genetics ; Phenotype ; Young Adult
    Chemical Substances Levodopa (46627O600J) ; COA7 protein, human
    Language English
    Publishing date 2023-09-26
    Publishing country Germany
    Document type Journal Article
    ZDB-ID 187050-6
    ISSN 1432-1459 ; 0340-5354 ; 0012-1037 ; 0939-1517 ; 1619-800X
    ISSN (online) 1432-1459
    ISSN 0340-5354 ; 0012-1037 ; 0939-1517 ; 1619-800X
    DOI 10.1007/s00415-023-11998-3
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top