达沙替尼治疗系统性硬化症相关间质性肺疾病中的新型肺成像生物标志物和皮肤基因表达亚型
系统性硬化症相关间质性肺疾病(SSc-ILD)达沙替尼治疗的临床数据,包含HRCT影像、皮肤基因表达、血清标志物和肺功能指标。

基本信息
资源简介
达沙替尼治疗系统性硬化症相关间质性肺疾病中的新型肺成像生物标志物和皮肤基因表达亚型
【数据集背景】
本数据集源站标题为《Novel lung imaging biomarkers and skin gene expression subsetting in dasatinib treatment of systemic sclerosis-associated interstitial lung disease》。配套论文《Novel lung imaging biomarkers and skin gene expression subsetting in dasatinib treatment of systemic sclerosis-associated interstitial lung disease》发表于 PLOS ONE(2017),DOI:10.1371/journal.pone.0187580。源站首次发布:2017-11-09。
【数据内容】
源站原始描述:Background There are no effective treatments or validated clinical response markers in systemic sclerosis (SSc). We assessed imaging biomarkers and performed gene expression profiling in a single-arm open-label clinical trial of tyrosine kinase inhibitor dasatinib in patients with SSc-associated interstitial lung disease (SSc-ILD). Methods Primary objectives were safety and pharmacokinetics. Secondary outcomes included clinical assessments, quantitative high-resolution computed tomography (HRCT)…
【数据结构与技术规格】
文件数 15 个,合计 1.96 MB。S1 Checklist.doc:application/msword,223.74 KB。S1 File.pdf:application/pdf,676.86 KB。S1 Table.docx:application/vnd.openxmlformats-officedocument.wordprocessingml.document,16.86 KB。数据集 DOI:10.1371/journal.pone.0187580。
【主题与分类】
源站学科分类:Biochemistry、Medicine、Cell Biology、Genetics、Molecular Biology、Pharmacology。主题标签:gene expression subset、target tissue-specific gene expression analyses、SSc-ILD dasatinib treatment、post-treatment skin biopsies、Inflammatory gene expression subset、day 169. Results Dasatinib、tyrosine kinase inhibitor dasatinib、serum biomarker assays、skin biopsy-based gene expression subset assignments、lung disease Background。
【适用方向】
多模态数据适合跨模态对齐、融合建模与联合表征学习方向的研究。
【获取与许可】
源站页面:https://plos.figshare.com/articles/dataset/Novel_lung_imaging_biomarkers_and_skin_gene_expression_subsetting_in_dasatinib_treatment_of_systemic_sclerosis-associated_interstitial_lung_disease/5587801
使用许可:CC BY 4.0(https://creativecommons.org/licenses/by/4.0/)。
规范引用:Martyanov, Viktor; Kim, Grace-Hyun J.; Hayes, Wendy; Du, Shuyan; Ganguly, Bishu J.; Sy, Oumar; et al. (2017). Novel lung imaging biomarkers and skin gene expression subsetting in dasatinib treatment of systemic sclerosis-associated interstitial lung disease. PLOS ONE. Dataset
【使用注意】
· 源站最后修改于 2023-06-02,引用时请注意版本时效。
下载信息
注册下载
需要注册 Kaggle 账号并登录后下载,适合需要跟踪下载记录和使用 API 的用户。
暂未开放公开下载
无需注册即可直接获取公开样本或文档,适合快速预览和评估数据集质量。
免登录有偿下载
公开数据集受托下载与技术交付服务。
提供高速下载与技术交付服务(收技术服务费,非数据销售)
暂未开放当前数据集主要来源为 Kaggle 公开托管,完整影像包建议通过原始链接或 Kaggle API 获取。
使用方式
数据集获取(Figshare)
- 源站标题:Novel lung imaging biomarkers and skin gene expression subsetting in dasatinib treatment of systemic sclerosis-associated interstitial lung disease
- DOI:10.1371/journal.pone.0187580
- 发布日期:2017-11-09
- 文件数:15 个
- 文件总体积:1.96 MB
- 源站页面:https://plos.figshare.com/articles/dataset/Novel_lung_imaging_biomarkers_and_skin_gene_expression_subsetting_in_dasatinib_treatment_of_systemic_sclerosis-associated_interstitial_lung_disease/5587801
命令行下载
curl -L -o "S1 Checklist.doc" "https://ndownloader.figshare.com/files/9719737"
curl -L -o "S1 File.pdf" "https://ndownloader.figshare.com/files/9719740"
curl -L -o "S1 Table.docx" "https://ndownloader.figshare.com/files/9719752"
curl -L -o "S2 Table.docx" "https://ndownloader.figshare.com/files/9719776"
curl -L -o "S3 Table.docx" "https://ndownloader.figshare.com/files/9719791"
curl -L -o "S4 Table.docx" "https://ndownloader.figshare.com/files/9719803"
curl -L -o "S5 Table.docx" "https://ndownloader.figshare.com/files/9719815"
curl -L -o "S6 Table.docx" "https://ndownloader.figshare.com/files/9719824"
文件清单
S1 Checklist.doc(223.74 KB)S1 File.pdf(676.86 KB)S1 Table.docx(16.86 KB)S2 Table.docx(14.42 KB)S3 Table.docx(14.34 KB)S4 Table.docx(15.13 KB)S5 Table.docx(15.49 KB)S6 Table.docx(14.30 KB)S7 Table.docx(14.82 KB)S8 Table.xlsx(85.33 KB)S9 Table.docx(15.25 KB)S10 Table.docx(14.71 KB)S1 Fig.pdf(117.85 KB)S2 Fig.pdf(346.62 KB)S3 Fig.pdf(375.61 KB)
文件总体积 1.96 MB(源站 API 实测)。
数据加载示例(图像类)
from PIL import Image
import glob, os
files = (glob.glob(os.path.join(path, "**", "*.png"), recursive=True)
+ glob.glob(os.path.join(path, "**", "*.jpg"), recursive=True)
+ glob.glob(os.path.join(path, "**", "*.tif"), recursive=True))
print("图像文件数:", len(files))
img = Image.open(files[0]); print("尺寸/模式:", img.size, img.mode)
# torchvision Dataset 方式:
# from torchvision import datasets
# ds = datasets.ImageFolder(path) # 要求 子目录=类别
目录组织与标注格式以源站说明和下载后实际文件为准。
数据说明
Background
There are no effective treatments or validated clinical response markers in systemic sclerosis (SSc). We assessed imaging biomarkers and performed gene expression profiling in a single-arm open-label clinical trial of tyrosine kinase inhibitor dasatinib in patients with SSc-associated interstitial lung disease (SSc-ILD).
Methods
Primary objectives were safety and pharmacokinetics. Secondary outcomes included clinical assessments, quantitative high-resolution computed tomography (HRCT) of the chest, serum biomarker assays and skin biopsy-based gene expression subset assignments. Clinical response was defined as decrease of >5 or >20% from baseline in the modified Rodnan Skin Score (MRSS). Pulmonary function was assessed at baseline and day 169.
Results
Dasatinib was well-tolerated in 31 patients receiving drug for a median of nine months. No significant changes in clinical assessments or serum biomarkers were seen at six months. By quantitative HRCT, 65% of patients showed no progression of lung fibrosis, and 39% showed no progression of total ILD. Among 12 subjects with available baseline and post-treatment skin biopsies, three were improvers and nine were non-improvers. Improvers mapped to the fibroproliferative or normal-like subsets, while seven out of nine non-improvers were in the inflammatory subset (p = 0.0455). Improvers showed stability in forced vital capacity (FVC) and diffusing capacity for carbon monoxide (DLCO), while both measures showed a decline in non-improvers (p = 0.1289 and p = 0.0195, respectively). Inflammatory gene expression subset was associated with higher baseline HRCT score (p = 0.0556). Non-improvers showed significant increase in lung fibrosis (p = 0.0313).
Conclusions
In patients with SSc-ILD dasatinib treatment was associated with acceptable safety profile but no significant clinical efficacy. Patients in the inflammatory gene expression subset showed increase in skin fibrosis, decreasing pulmonary function and worsening lung fibrosis during the study. These findings suggest that target tissue-specific gene expression analyses can help match patients and therapeutic interventions in heterogeneous diseases such as SSc,
许可
CC BY 4.0
引用
学术使用请引用 DOI 10.1371/journal.pone.0187580(source: https://plos.figshare.com/articles/dataset/Novel_lung_imaging_biomarkers_and_skin_gene_expression_subsetting_in_dasatinib_treatment_of_systemic_sclerosis-associated_interstitial_lung_disease/5587801)。
数据缺失?
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