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Glucose metabolism in Familial Hypobetalipoproteinemia

Recruiting
Conditions
patients with familial hypobetalipoproteinemia and matched controls
Registration Number
NL-OMON29272
Lead Sponsor
-
Brief Summary

/A

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
16
Inclusion Criteria

1. Subjects with documented FHBL, who have liver steatosis (FHBL group).
Healthy subjects (control group), exactly matched for age, sex, body mass index, waist circumference and physical activity

Exclusion Criteria

1. Known any somatic illness, including neoplasm, metabolic or endocrine disorder, neurologic disorder, active infection, or recent surgical procedures within 3 months of study initiation.

2. Use of medication, which can influence glucose or FFA metabolism (insuline, anabolic steroids, growth hormone, testosteron, DHEA, statines, ACE-inhibitors, AII-antagonists, aspirin)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To determine in detail:<br /><br>1) Quantity of liver- and muscle triglycerides<br /><br>2) Body fat distribution<br /><br>3) hepatic insulin sensitivity<br /><br>4) peripheral insulin sensitivity <br /><br>5) intramyocellular differences regarding fatty acid handling<br>of drug-free subjects with FHBL as compared to healthy controls matched for age, sex, body mass index, waist circumference and physical activity.<br>
Secondary Outcome Measures
NameTimeMethod
Adiponectin levels and levels of different adiponectin forms in plasma.
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