Atorvastatin Therapy on Xanthoma in Alagille Syndrome
Alagille Syndrome, Atorvastatin, Xanthoma
About this trial
This is an interventional treatment trial for Alagille Syndrome
Eligibility Criteria
Inclusion Criteria:
Meet the ALGS diagnostic criteria;
Xanthoma of skin; ③ Before treatment with atorvastatin, LDL-C≥4.9mmol/L(190 mg/dL); ④ Informed consent; ⑤ Age 0-17 years old, male or female;
- Taking bile acid chelator (colenemide) has no obvious effect or intolerance.
Exclusion Criteria:
Liver transplantation has been performed;
In the recovery period of cholestasis, xanthoma is obviously subsiding;
Patients with serious systemic diseases and unstable vital signs;
④ Progressive active liver injury, such as continuous increase of transaminase;
Serious myopathy;
⑥ Known to be allergic to any component of atorvastatin.
Sites / Locations
- Children's Hospital of Fudan UniversityRecruiting
Arms of the Study
Arm 1
Experimental
Atorvastatin+ALGS-Xanthoma
Drug: atorvastatin Dosage form: tablet Route of administration: oral Duration: 6 months (After 6 months of medication, according to the actual situation of the patient, choose to maintain the original dosage, gradually reduce the dosage or stop the medication) Administration method: Initial dose: ① < 1 year old: 1.25mg/d, qd; ② 1-5 years old: 2.5mg/d, qd; ③ 6-9 years old: 5mg/d, qd; ④ ≥ 10 years old: 10mg/d, qd. The maximum dose is 40mg/d and not more than 1mg/kg/d. During the follow-up, the medication was adjusted according to the laboratory results until non-HDL-C≤4.2mmol/L(162 mg/dL), xanthoma disappear, or the patient had moderate or more serious adverse reactions.