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NCT Number: NCT06584565

A Multicenter Study Based on Multi-omics Analysis to Predict the Early Prognosis and Recurrence Risk of Acute Ischemic Stroke

Through a multicenter prospective AIS cohort study, we analyze the potential association of human proteome, microbiome and metabolome alterations with AIS prognosis, searching for key proteins, differential organisms and metabolites, combining experimental data at multiple molecular levels with computational models, and establishing early prediction models through machine learning-based prediction algorithms. While closely tracking the recurrence of stroke in AIS patients, we evaluate the predictive value of human proteome, microbiome and metabolites for stroke recurrence through a nested case-control study, which provides key reference information for exploring the unknown residual risk of AIS recurrence.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Nanfang Hospital,Southern Medical University

Guangzhou, Guangdong, 510515, China

Location status: Recruiting

Location contact

Jia Yin, M.D

CONTACT

[email protected]

13802964883

About this study

Currently, the burden of brain vascular disease in China is the highest in the world, and among them, the incidence rate of acute ischemic stroke (AIS) is high, the recurrence rate is high, the disability rate is high, the mortality rate is high, and the social burden is heavy. With the increasing number of AIS patients, how to effectively prevent and treat them is a huge challenge facing us. The occurrence and development of AIS are caused by the joint action of multiple risk factors and mutual influence, and single technical means are difficult to deeply explore its complex mechanism. Therefore, building a risk prediction model for poor prognosis and recurrence based on multi-omics technology and layering risk factors for patients are the important research directions for the future. This study aims to establish a multi-center cohort by collecting fecal and blood samples from AIS patients and conducting proteomic, microbial and metabolomic detection. It records the prognosis and recurrence events and uses cross-omics analysis technology to explore the multi-omics network molecular mechanism and screen for new intervention targets. It establishes an early prediction model and explores the stroke secondary prevention strategy based on multi-omics data.

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Meet the diagnostic criteria of AIS according to the Chinese Guidelines for the Diagnosis and Treatment of Acute Ischemic Stroke 2018
  • Aged 18 to 75 years old
  • Stroke within 7 days of onset
  • Sign informed consent, provide relevant medical history information and provide biological specimens

Exclusion criteria

  • Severe impairment of consciousness (awareness score of NIHSS>1)
  • History of stroke within 12 months
  • Severe systemic disease including malignancy
  • ALT or AST> 2 times the upper limit of normal or severe liver disease
  • creatinine > 1.5 times the upper limit of normal or severe kidney disease
  • History of long-term drinking, drug use, and chemical poisoning (e.g., pesticide poisoning); Note: Long-term alcohol consumption, usually more than 5 years, over 40 g/day of alcohol for men and 20 g/day for women, or a history of heavy alcohol consumption within 2 weeks, over 80 g/day of alcohol
  • History of intestinal tumors, irritable bowel syndrome or inflammatory bowel disease or confirmed in the hospital
  • Unable to collect a stool specimen within 4 days of admission
  • Assessed to be unsuitable for participation in this study by the investigator

Treatment and study plan

microbiome; metabolomics; proteomics

Other

post-stroke change of microbiome; metabolomics; proteomics

Primary outcomes

  1. Incidence of new cardiovascular events and death

    Time frame: within 12 months after onset

    any stroke /TIA/ myocardial infarction/Vascular death

Secondary outcomes

  1. Brain Injury Conditions

    Time frame: 3, 12 months after ischemic stroke

    Clinical investigators evaluate brain injury conditions according to head CT or MR, which including the signs of infarct lesions, hemorrhagic transformation post-infarction or cerebral edema.

  2. Small Vessel Disease Burden

    Time frame: 3, 12 months after ischemic stroke

    Clinical investigators evaluate small vessel disease burden according to head CT or MR, which including the signs of white matter degeneration, lacunar infarctions, cerebral microbleeds or enlarged perivascular spaces.

  3. Cerebrovascular Pathology

    Time frame: 3, 12 months after ischemic stroke

    Clinical investigators evaluate cerebrovascular pathology according to head CT or MR, which including the signs of vascular stenosis, vascular dissection or collateral circulation compensation.

  4. Modified Rankin Scale ( mRS ) score

    Time frame: 7 day and 3, 12 months after ischemic stroke

    The MRS score is primarily used to measure the degree of disability and daily living ability of patients. The MRS score ranges from 0 to 6, with a total of 7 levels. The higher the score, the more severe the disability and the worse the prognosis.

  5. National Institutes of Health Stroke Scale ( NIHSS ) score

    Time frame: 7 day and 3, 12 months after ischemic stroke

    The NIHSS score is commonly used to assess the degree of neurological impairment in patients with acute stroke. The NIHSS consists of 11 items, with a total score ranging from 0 to 42. Each item has different scoring criteria, typically ranging from 0 (normal) to 4 (most severe).

  6. Activity of Daily Living Scale ( ADL ) score

    Time frame: 7 day and 3, 12 months after ischemic stroke

    The ADL score is primarily used to measure a person's ability to perform basic daily activities. This study uses the Barthel Index scoring method, which ranges from 0 to 100 points, with scoring items including eating, bathing, grooming, dressing, bowel control, bladder control, toileting, transferring, mobility and stairs. A higher score indicates greater independence, while a lower score indicates greater dependence.

  7. Mini-mental State Examination ( MMSE ) score

    Time frame: 3, 12 months after ischemic stroke

    The MMSE (Mini-Mental State Examination) is a tool used to assess cognitive function, including orientation, memory, attention, language skills, calculation ability, and visuospatial skills. It is commonly used to screen for dementia in older adults. The MMSE has a total score of 30 points: a score of 24-30 suggests normal cognitive function, 18-23 indicates mild cognitive impairment, and 0-17 indicates moderate to severe cognitive impairment.

  8. Montreal Cognitive Assessment ( MOCA ) score

    Time frame: 3, 12 months after ischemic stroke

    The MoCA is a tool used to assess cognitive impairment. Compared to the MMSE, the MoCA is more sensitive, particularly for detecting mild cognitive impairment (MCI). The MoCA has a total score of 30 points: a score of 26-30 suggests normal cognitive function, 18-25 indicates mild cognitive impairment (MCI), and 0-17 indicates moderate to severe cognitive impairment. Typically, individuals with lower educational levels (less than 12 years of education) receive an additional point as an adjustment to their total score.

  9. Hamilton Depression Scale ( HAMD ) score

    Time frame: 3, 12 months after ischemic stroke

    The HAMD is a clinical scale used to assess the severity of depression. This study uses the 17-item version (HAMD-17), which covers a range of symptoms, including mood, sleep, appetite, and somatic symptoms. The total score ranges from 0 to 52, with each item rated based on the severity of symptoms, typically from 0 (no symptoms) to 4 (severe symptoms).

  10. Hamilton Anxiety Scale ( HAMA ) score

    Time frame: 3, 12 months after ischemic stroke

    The HAMA is a clinical scale used to assess the severity of anxiety symptoms. It consists of 14 items, each evaluating different symptoms related to anxiety. These symptoms cover both psychological and somatic manifestations of anxiety. Each item is rated based on the severity of symptoms, with scores ranging from 0 (no symptoms) to 4 (very severe symptoms).

Study contacts

Contact information is provided by the study sponsor or research team.

Jia Yin, M.D

CONTACT

[email protected]

13802964883

Weike Hu, M.D

CONTACT

[email protected]

18326349212

Sponsors and collaborators

Lead sponsor

Nanfang Hospital, Southern Medical University

Other

Registry information

Important dates

Study start
2024
Primary completion
2028
Study completion
2028
First posted
Sep 5, 2024
Registry last updated
Sep 5, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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