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Establishment of Disease Characteristics and a Chinese Medicine Prognosis Risk Model Based on a Large-Scale Database After Coronary Revascularization

2026年5月21日 更新者:Liu Qiang
This study aims to develop a risk prediction model for patients who have undergone coronary revascularization (such as stent placement or bypass surgery). After these procedures, some patients still experience heart-related problems like chest pain, heart attack, or rehospitalization. This study will enroll 600 patients from multiple hospitals in China and follow them for 12 months. At enrollment and at 12, 24, 36, and 48 weeks after surgery, researchers will collect clinical information (including traditional Chinese medicine symptoms, blood tests, heart imaging) and biological samples (blood and tongue coating). Using artificial intelligence, the study will build a predictive model that combines Western medical data with traditional Chinese medicine characteristics. The goal is to better identify patients at higher risk of future heart events, so that personalized prevention and management can be provided. The study does not involve any experimental treatment or intervention - it is purely observational.

調査の概要

状態

まだ募集していません

詳細な説明

This is a multicenter, prospective cohort study conducted at five sites in China. The study aims to develop and validate a prognostic risk model for major adverse cardiovascular events (MACE) in patients after coronary revascularization (percutaneous coronary intervention or coronary artery bypass grafting).

Study population: A total of 600 eligible patients aged ≥18 years who have undergone coronary revascularization will be enrolled consecutively. Key exclusion criteria include severe heart failure, malignant arrhythmias, severe pulmonary or liver/kidney dysfunction, pregnancy, psychiatric disorders, and poor compliance.

Data collection: At baseline (enrollment), the following data are collected: demographics, medical history, surgical characteristics (e.g., access route, number of stents, target vessels), vital signs, laboratory tests (complete blood count, cardiac enzymes, liver/kidney function, lipids, glucose), echocardiography, 24-hour ambulatory electrocardiography, and a standardized Traditional Chinese Medicine (TCM) case report form covering symptom scores, tongue/pulse findings, and pattern elements. In addition, biological samples (blood and tongue coating) are obtained for proteomics, metabolomics, and tongue-coating microbiomics.

Follow-up: Participants are followed at 12, 24, 36, and 48 weeks post-enrollment. At each follow-up, the TCM case report form is reassessed, MACE (including all-cause death, subacute stent thrombosis, perioperative myocardial infarction, recurrent myocardial infarction, recurrent unstable angina, repeat revascularization, and rehospitalization for angina or heart failure) are recorded, and NYHA functional class and current medications are updated.

Statistical analysis: Missing data will be handled by mean imputation or K-nearest neighbors imputation. Continuous variables will be standardized using Z-scores, and categorical variables will be one-hot encoded. Feature selection will be performed using LASSO regression. Three nested prediction models will be built:

  • Model_Base: Cox proportional hazards model based on routine clinical and imaging variables.
  • Model_TCM: adding TCM syndrome features using machine learning algorithms (random forest, support vector machine).
  • Model_Full: further integrating multi-omics biomarkers using deep learning methods (convolutional neural network, transformer).

Model performance will be assessed by discrimination (area under the ROC curve), calibration, and decision curve analysis. Internal validation will use k-fold cross-validation, and external validation will be conducted in at least three independent hospitals. The targeted predictive accuracy (area under the curve) is above 85%. All analyses will be performed using SPSS 26.0, Python, and R.

Ethics: The study protocol has been approved by the ethics committee of the lead site (The Third Affiliated Hospital of Zhejiang Chinese Medical University) and will be approved by participating centers. Written informed consent will be obtained from all participants.

研究の種類

観察的

入学 (推定)

600

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

サンプリング方法

確率サンプル

調査対象母集団

Adult patients (≥18 years) who have undergone coronary revascularization (percutaneous coronary intervention or coronary artery bypass grafting) for coronary artery disease. Participants are recruited consecutively from the cardiology wards and outpatient clinics of three tertiary hospitals in China, including The Third Affiliated Hospital of Zhejiang Chinese Medical University (lead site), Zhejiang Provincial People's Hospital, The First Affiliated Hospital of Zhejiang Chinese Medical University.

説明

Inclusion Criteria:

  • Diagnosis of coronary artery disease with prior coronary revascularization (PCI or CABG)
  • Age ≥ 18 years
  • Signed informed consent

Exclusion Criteria:

  • Malignant arrhythmias, severe heart failure, myocardial disease, or structural heart disease
  • Severe pulmonary insufficiency, severe liver or kidney dysfunction, severe electrolyte disturbances
  • Pregnancy or breastfeeding
  • Severe psychiatric disorders, malignant tumors, hematologic diseases, rheumatic immune diseases, or severe infection
  • Poor compliance or any other reason making the participant unsuitable for the study

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

コホートと介入

グループ/コホート
Adults post-coronary revascularization.
Patients aged ≥18 years who underwent coronary revascularization (PCI or CABG). Consecutive enrollment from 5 Chinese hospitals. Prospective follow-up at 12, 24, 36, and 48 weeks post-enrollment. Assessments include MACE (all-cause death, stent thrombosis, myocardial infarction, unstable angina, repeat revascularization, rehospitalization), TCM syndrome score, NYHA class, echocardiography, ambulatory ECG, and biospecimens (blood and tongue coating for proteomics, metabolomics, microbiomics). No intervention is assigned.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Major Adverse Cardiovascular Events (MACE)
時間枠:12, 24, 36, and 48 weeks post-enrollment
Composite of all-cause death, subacute stent thrombosis, perioperative myocardial infarction, recurrent myocardial infarction, recurrent unstable angina, repeat revascularization (PCI or CABG), and rehospitalization due to angina or heart failure. Events are ascertained by medical records, clinical diagnosis, coronary angiography, ECG, and cardiac enzyme/troponin measurements.
12, 24, 36, and 48 weeks post-enrollment

二次結果の測定

結果測定
メジャーの説明
時間枠
Traditional Chinese Medicine (TCM) Syndrome Score
時間枠:Baseline, 12, 24, 36, 48 weeks post-enrollment
Total score of TCM symptoms and signs (chest pain, palpitations, fatigue, tongue/pulse, etc.). Each item scored 0-3 (none to severe). Sum of all items. Higher score indicates more severe symptoms. Unit of Measure: points on a scale
Baseline, 12, 24, 36, 48 weeks post-enrollment
NYHA Functional Class
時間枠:12, 24, 36, 48 weeks post-enrollment
Classification of heart failure symptoms based on physical activity limitation. Class I (no limitation) to IV (symptoms at rest). Unit of Measure: relative abundance / qualitative
12, 24, 36, 48 weeks post-enrollment
Multi-omics Biomarkers (exploratory)
時間枠:Baseline
Proteomics, metabolomics (LC-MS/MS, LC-MS/GC-MS) from blood, and 16S rRNA microbiome from tongue coating. Used to identify biomarkers associated with TCM patterns. Results reported as relative abundance or presence/absence. Unit of Measure: relative abundance / qualitative
Baseline
Left Ventricular End-Diastolic Diameter (LVEDD)
時間枠:Baseline
Diameter of the left ventricle at end-diastole, measured by echocardiography. Unit of Measure: mm.
Baseline
Left Ventricular End-Systolic Diameter (LVESD)
時間枠:Baseline
Diameter of the left ventricle at end-systole, measured by echocardiography. Unit of Measure: mm
Baseline
Left Ventricular Posterior Wall Thickness (LVPW)
時間枠:Baseline
Thickness of the left ventricular posterior wall in diastole, measured by echocardiography. Unit of Measure: mm.
Baseline
Interventricular Septal Thickness (IVS)
時間枠:Baseline
Thickness of the interventricular septum in diastole, measured by echocardiography. Unit of Measure: mm
Baseline
Left Ventricular Ejection Fraction (LVEF)
時間枠:Baseline
Percentage of blood ejected from the left ventricle per contraction, measured by echocardiography. Unit of Measure: %.
Baseline
Left Ventricular Fractional Shortening (FS)
時間枠:Baseline
Percentage change in left ventricular diameter between diastole and systole, measured by echocardiography. Unit of Measure: %
Baseline
E/A Ratio
時間枠:Baseline
Ratio of early (E) to late (A) ventricular filling velocities, measured by pulsed-wave Doppler echocardiography. Unit of Measure: ratio
Baseline
Mean Heart Rate (24-hour)
時間枠:Baseline
Average heart rate over 24 hours derived from ambulatory electrocardiography (Holter). Unit of Measure: beats per minute (bpm)
Baseline
Minimum Heart Rate (24-hour)
時間枠:Baseline
Lowest heart rate recorded during 24-hour ambulatory ECG, with timestamp. Unit of Measure: bpm.
Baseline
Maximum Heart Rate (24-hour)
時間枠:Baseline
Highest heart rate recorded during 24-hour ambulatory ECG, with timestamp. Unit of Measure: bpm.
Baseline
Total Premature Ventricular Contractions (PVCs)
時間枠:Baseline
Number of premature ventricular contractions recorded over 24 hours by ambulatory ECG. Unit of Measure: count per 24h
Baseline
Total Premature Atrial Contractions (PACs)
時間枠:Baseline
Number of premature atrial contractions recorded over 24 hours by ambulatory ECG. Unit of Measure: count per 24h
Baseline
Maximum RR Interval
時間枠:Baseline
Longest interval between two consecutive R waves on 24-hour ambulatory ECG, indicating cardiac pause. Unit of Measure: seconds (s)
Baseline
ST Segment Depression Maximum Amplitude
時間枠:Baseline
Greatest magnitude of ST segment depression during any ischemic event on 24-hour ambulatory ECG. Unit of Measure: mm (or mV)
Baseline
ST Segment Depression Longest Duration
時間枠:Baseline
Longest duration of a single ST segment depression event on 24-hour ambulatory ECG. Unit of Measure: minutes (min)
Baseline
SDNN (Heart Rate Variability)
時間枠:Baseline
Standard deviation of all normal-to-normal R-R intervals over 24 hours, a measure of heart rate variability. Unit of Measure: milliseconds (ms)
Baseline

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研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年7月1日

一次修了 (推定)

2028年6月30日

研究の完了 (推定)

2028年12月31日

試験登録日

最初に提出

2026年5月15日

QC基準を満たした最初の提出物

2026年5月21日

最初の投稿 (実際)

2026年5月29日

学習記録の更新

投稿された最後の更新 (実際)

2026年5月29日

QC基準を満たした最後の更新が送信されました

2026年5月21日

最終確認日

2026年5月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • ZSLL-KY-2026-027-01

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

IPD プランの説明

Individual participant data (IPD) will not be shared because the informed consent obtained from participants did not include provisions for data sharing beyond the primary study. Additionally, the data contain sensitive clinical information and biospecimen-derived multi-omics data, which may raise privacy and ethical concerns. Access to de-identified data may be considered upon reasonable request to the principal investigator, subject to institutional and ethics committee approval.

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