Publications by authors named "Koichi Ashizaki"

Background: Persistent facial erythema represents a significant complication in atopic dermatitis (AD) patients undergoing treatment with dupilumab. Stratifying patients based on the erythema course is crucial for elucidating heterogeneous phenotypes and facilitating advanced drug efficacy predictions.

Objectives: This study aimed to identify factors associated with facial erythema severity in dupilumab-treated AD patients and to establish a prediction model for drug response based on the identified factors.

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Background: In clinical research on multifactorial diseases such as atopic dermatitis, data-driven medical research has become more widely used as means to clarify diverse pathological conditions and to realize precision medicine. However, modern clinical data, characterized as large-scale, multimodal, and multi-center, causes difficulties in data integration and management, which limits productivity in clinical data science.

Methods: We designed a generic data management flow to collect, cleanse, and integrate data to handle different types of data generated at multiple institutions by 10 types of clinical studies.

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Article Synopsis
  • - Atopic dermatitis (AD) is not just a local skin issue but a complex systemic disease, showing varying clinical presentations and molecular profiles based on patient data.
  • - Researchers analyzed RNA-sequencing data from both skin and blood samples of 115 AD patients and 14 healthy controls to identify specific molecular features linked to different clinical manifestations, like erythema and papulation.
  • - By using a regression model on longitudinal data from 30 AD patients, they discovered three distinct patient clusters relating to clinical severity and treatment history, emphasizing the need for a comprehensive approach in understanding and monitoring AD.
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For eradication of HIV-1 infection, it is important to elucidate the detailed features and heterogeneity of HIV-1-infected cells in vivo. To reveal multiple characteristics of HIV-1-producing cells in vivo, we use a hematopoietic-stem-cell-transplanted humanized mouse model infected with GFP-encoding replication-competent HIV-1. We perform multiomics experiments using recently developed technology to identify the features of HIV-1-infected cells.

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