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Building a Clinical Predictive Model for Patients with Cardiorenal Syndrome and Type 2 Diabetes Based on Lipid Toxicity Using oxLDL as the Core

Building a Clinical Predictive Model for Patients with Cardiorenal Syndrome and Type 2 Diabetes Based on Lipid Toxicity Using oxLDL as the Core

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121914
Enrollment
Unknown
Registered
2026-04-07
Start date
2026-05-01
Completion date
Unknown
Last updated
2026-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiorenal Syndrome

Interventions

Sponsors

Guang'anmen Hospital of China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Age >=18 years, no gender restrictions; 2. Meets the diagnostic criteria for CRS (as outlined in the 2021 Clinical Practice Guidelines for the Diagnosis and Treatment of Cardiorenal Syndrome issued by the Division of Nephrology of the Chinese Medical Doctor Association and the 2019 American Heart Association Scientific Statement on Cardiorenal Syndrome: Classification, Pathophysiology, Diagnosis, and Treatment Strategies: Scientific Statement of the American Heart Association"): Patients must have an estimated glomerular filtration rate (eGFR) 133 µmol/L, and NT-proBNP >=1200 ng/L; 3. T2D diagnosis follows the Chinese Diabetes Prevention and Treatment Guidelines 2024 Edition: Typical symptoms (polydipsia, polyphagia, polyuria, weight loss) + random blood glucose >=11.1 mmol/L, or fasting blood glucose>=7.0 mmol/L, or OGTT 2h glucose >=11.1 mmol/L, or HbA1c >=6.5%; Patients without typical symptoms require confirmation via follow-up testing; 4. Patients in retrospective studies must have suitable biological specimens on file; 5. Ethical approval for the use of medical records and biological specimens.

Exclusion criteria

Exclusion criteria: 1. Familial hypercholesterolemia and hypertriglyceridemia; 2. Type 1 diabetes and secondary diabetes; 3. Primary liver disease with transaminase levels more than three times elevated; 4. Patients undergoing continuous hemodialysis; 5. Concurrent severe infection, acute cardiovascular or cerebrovascular disease, uncontrolled thyroid disease, malignancy, or primary severe anemia (Hb < 60 g/L); 6. Pregnant or lactating women; 7. Individuals with psychiatric disorders unable to cooperate with data collection and follow-up.

Design outcomes

Primary

MeasureTime frame
Age;Gender;Course of disease;Body Mass Index;Systolic Blood Pressure;Diastolic Blood Pressure;Fasting Plasma Glucose;Glycated Hemoglobin;Total Cholesterol;Triglyceride;High-Density Lipoprotein Cholesterol;Low-Density Lipoprotein Cholesterol;N-Terminal Pro-B-Type Natriuretic Peptide;Blood Urea Nitrogen;Serum Creatinine;estimated Glomerular Filtration Rate;High-Sensitivity C-Reactive Protein;oxidized Low-Density Lipoprotein;Ceramides;Glutathione Peroxidase 1;F2a8-Isoprostaglandin F2a;Epicardial Fat Thickness;Podocalyxin;Fasting Insulin;Homeostasis Model Assessment of Insulin Resistance;Urine Protein;Urine Microalbumin;Urine Microalbumin Creatinine Ratio;

Secondary

MeasureTime frame
Smoking history;Drinking history;Family history;Heart Rate;Lipoprotein a;Apolipoprotein A;Apolipoprotein B;

Countries

China

Contacts

Public ContactZhou YuPing

Guang'anmen Hospital of China Academy of Chinese Medical Sciences

zhouyuping@gamyy.cn+86 139 1145 6307

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026