Study of Tacrolimus Used for Pediatric Patients With Nephrotic Syndrome Based on Pharmacogenomics and Metabonomics
- Conditions
- Nephrotic Syndrome
- Interventions
- Other: therapeutic drug monitoring
- Registration Number
- NCT02602873
- Lead Sponsor
- Guangzhou Women and Children's Medical Center
- Brief Summary
Tacrolimus is recommended to be the first line therapeutic medication within the several immunosuppressive agents when treating refractory pediatric nephrotic syndrome, because of its definite efficacy and low toxicity. But there are still some key problems which hinder the using of tacrolimus in clinic, such as its narrow therapeutic widow, great individual difference of pharmacokinetics. Routine therapeutic drug monitoring(TDM) is needed in practice. But the disadvantage of TDM is hysteresis, which could lead to treatment failure or toxicity. To find out the reasons of great pharmacokinetic difference between patients and find out the individual proper dosage before administration are important for the clinical using of tacrolimus.
It is hot in research of tacrolimus in organ transplant field, such as the association between gene polymorphisms of cytochrome P-450 3A4, 3A5 and multiple drug resistant gene(MDR1) and concentration of tacrolimus. However, there is few study about pharmacogenomics and metabonomics of tacrolimus in patients of nephrotic syndrome.
The aim is to study the relationships between pharmacogenomics, metabonomics of tacrolimus and its efficacy, toxicity and blood concentration in patients of nephrotic syndrome, to find out the exact dosage before administration, to provide reference to individual drug administration.
- Detailed Description
Investigators will collect data about efficacy and adverse drug reaction(ADR) such as time of efficacy when evaluated, how to evaluate ADR, data of demography, etc.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 150
- patients with refractory nephrotic syndrome;
- patients age ≤14y.
- patients are sensitive to steroid;
- combined therapy with other immunosuppressive agent;
- combined using drugs which maybe interact the concentration of tacrolimus;
- with other malignant disease, such as tumor.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description good efficacy therapeutic drug monitoring using therapeutic drug monitoring to adjust the dose of tacrolimus. patients can reach effective outcome. poor efficacy therapeutic drug monitoring using therapeutic drug monitoring to adjust the dose of tacrolimus. patients can not reach effective outcome.
- Primary Outcome Measures
Name Time Method "Genotypes as measured by polymerase chain reaction-restriction fragment length polymorphism" 1 week genotype are collected from hospital system.
"Concentration as measured by liquid chromatography mass spectrometry" 1 week concentration of tacrolimus are collected from hospital system.
"Relationship between genotypes and concentration as analyzed at 1 week" 1 week using Statistic Package for Social Science 21.0 software to analyze the relationship between gene polymorphism and concentration.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Guangzhou women and children's medical center
🇨🇳Guangzhou, Guangdong, China
Guangzhou women and children's medical center🇨🇳Guangzhou, Guangdong, China