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临床试验/NCT07140601
NCT07140601招募中不适用

Environmental Pollutants and Neurological Disorders: Clinical and Mechanistic Study

Beijing Tiantan Hospital1 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2025年8月1日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
500
试验地点
1
主要终点
Overall Survival (OS)

研究概览

简要总结

Environmental pollutants have emerged as a major global health concern, with growing evidence linking exposure to both traditional contaminants such as heavy metals (lead, mercury, cadmium, arsenic) and novel pollutants-including micro- and nanoplastics, per- and polyfluoroalkyl substances (PFAS), antibiotics, and endocrine-disrupting chemicals-to adverse neurological outcomes. These pollutants can cross or disrupt the blood-brain barrier, accumulate in neural tissue, and trigger oxidative stress, inflammation, epigenetic modifications, and metabolic reprogramming.

Brain tumours and cerebrovascular diseases represent two major categories of neurosurgical disorders with high morbidity and mortality. However, their interaction with environmental pollutant exposure remains poorly understood. Recent studies suggest that pollutant-induced molecular alterations, such as aberrant DNA methylation, lipid metabolism disruption, and neurovascular endothelial dysfunction, may contribute to tumour initiation, malignant progression, aneurysm formation, and stroke occurrence.

Given the increasing human exposure to these pollutants and the lack of large-scale clinical data, it is urgent to establish a systematic investigation in neurosurgical patients. This study aims to profile pollutant exposure (heavy metals, PFAS, microplastics, and other novel contaminants) using multi-biospecimen analysis (blood, urine, hair, tumour and peri-tumour tissues), and to explore their mechanistic links to the pathogenesis of brain tumours and cerebrovascular diseases. The findings are expected to provide new evidence for understanding environment-brain interactions and to identify potential biomarkers for disease risk stratification and prevention.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18 years of age or older;
  • Able to give informed consent to participate in the research.

排除标准

  • Refusal to participate.
  • Pregnant or breastfeeding woman.

结局指标

主要结局

Overall Survival (OS)

时间窗: Until death or study completion (24 months)

OS is defined as the time from the sample collection date to death due to any cause. All other participants will be censored at the last date known to be alive.

次要结局

  • Progression-Free Survival (PFS)(Until progression or death or study completion (24 months))
  • modified Rankin Scale (mRS)(90 days after sample collection)

研究者

发起方
Beijing Tiantan Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Xiaolin Chen, MD

Prof.

Beijing Tiantan Hospital

研究点 (1)

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