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临床试验/NCT07055269
NCT07055269进行中(未招募)不适用

Assessment of Liver Metabolic Alterations in Vivo in Patients With Citrin Deficiency and Healthy Subjects by Metabolic Labeling With Stable Isotopes

Johannes Haeberle1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2025年10月20日最近更新:
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
20
试验地点
1
主要终点
Liver metabolic flux

研究概览

简要总结

Citrin is an aspartate-glutamate transporter in the liver that facilitates the urea cycle pathway for ammonia detoxification via ureagenesis. It is also thought to be involved in liver energy metabolism as a component of the malate-aspartate shuttle. The clinical presentation in patients supports the hypothesis that liver glycolytic, gluconeogenic and lipogenic functions are compromised in citrin deficiency, but none of the key hepatic pathway fluxes have been measured in patients to date. This is the first study that will examine the liver metabolic fluxes in patients with citrin deficiency.

Liver metabolic functions will be examined by metabolic flux assays and biochemical measurements after application of stable isotopes 2H2O and [U-13C6]-fructose. Urea cycle metabolites and their enrichment after application of a stable isotope tracer 15NH4Cl will be measured to examine the liver's ability to detoxify ammonia into urea.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • for AACD patients are:
  • Subjects with citrin deficiency, confirmed by genetic analysis to carry pathogenic variant(s) in the SLC25A13 gene
  • Age from 18 years to 65 years inclusive
  • Male or female
  • Written informed consent has been given
  • Understands and is willing, able and likely to comply with study procedures and restrictions
  • Inclusion criteria for healthy subjects are:
  • Age from 18 years to 65 years inclusive, and not more than five years younger or older than the specified paired participant from the AACD group
  • Same sex as the specified paired participant from the AACD group
  • Same ethnicity the specified paired participant from the AACD group
  • Written informed consent has been given
  • Understands and is willing, able and likely to comply with study procedures and restrictions

排除标准

  • for AACD patients are:
  • acute and chronic disease requiring treatment of any kind, other than his/her AACD
  • females who are pregnant or lactating or attempting to become pregnant
  • use of any medication which, in the opinion of the investigator, is likely to interfere with liver function
  • Exclusion criteria for healthy subjects are:
  • carry any pathogenic variant in the SLC25A13 gene
  • current or recurrent disease that could affect the metabolic function of the liver
  • acute and chronic disease requiring treatment of any kind
  • females who are pregnant or lactating or attempting to become pregnant
  • use of any medication which, in the opinion of the investigator, is likely to interfere with liver function
  • weight loss ≥10% within 3 months before study screening
  • daily alcohol consumption of more than 2 standard-sized beer for men and more than 1 standard-sized beer for women, or the equivalent
  • BMI > 30 kg/m2
  • currently smoking >1 cigarette daily
  • liver transplant recipients
  • type 1 and 2 diabetes
  • currently on a ketogenic diet
  • currently taking medium chain triglyceride (MCT) supplements

研究组 & 干预措施

AACD patient

Experimental

isotope tracer for ureagenesis and liver metabolic flux

干预措施: ureagenesis capacity (Other)

healthy volunteer

Experimental

isotope tracer for ureagenesis and liver metabolic flux

干预措施: liver metabolic flux (Other)

AACD patient

Experimental

isotope tracer for ureagenesis and liver metabolic flux

干预措施: liver metabolic flux (Other)

结局指标

主要结局

Liver metabolic flux

时间窗: 5 days

Liver metabolic flux will be measured by assessing the distribution of the administered isotope tracers \[U-13C6\]-fructose and heavy water.

次要结局

  • Ureagenesis capacity(1 day)
  • adverse events(5 days)
  • liver fat content(1 day)
  • Liver fibrosis(1 day)
  • Clinical symptoms(1 day)

研究者

发起方
Johannes Haeberle
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Johannes Haeberle

Head of Metabolic Laboratory

University Children's Hospital, Zurich

研究点 (1)

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