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A Familial Hypercholesterolemia Human Liver Chimeric Mouse Model Using Induced Pluripotent Stem Cell-derived Hepatocytes
Published on: September 15, 2018
Primary hypocholesterolemia is associated with an increased risk of hepatic complications in the general population
Matthieu Wargny1, Thomas Goronflot2, Antoine Rimbert3
1Nantes Université, CHU Nantes, CNRS, Inserm, l'institut du thorax, F-44000 Nantes, France; Nantes Université, CHU Nantes, Pôle Hospitalo-Universitaire 11: Santé Publique, Clinique des données, INSERM, CIC 1413, F-44000 Nantes, France.
Insights
Individuals with hypobetalipoproteinemia (HBL), a condition of low LDL-C, face a significantly higher risk of liver complications, including cancer. This finding highlights the need for targeted liver monitoring in HBL patients.
Area of Science:
- Cardiovascular and Metabolic Medicine
- Hepatology
- Genetics and Genomics
Background:
- Low-density lipoprotein-cholesterol (LDL-C) health effects beyond cardiovascular protection are debated.
- Primary hypobetalipoproteinemia (HBL) is linked to potential hepatic steatosis and cirrhosis.
- Investigating HBL's association with hepatic complications is crucial.
Purpose of the Study:
- To assess the risk of hepatic complications in individuals with primary hypobetalipoproteinemia (HBL).
- To determine if HBL is an independent risk factor for liver diseases like cirrhosis and primary liver cancer.
Main Methods:
- A comparative cohort study design was employed using the French CONSTANCES and UK Biobank (UKBB) cohorts.
- Participants with HBL (LDL-C <5th percentile) were compared to controls with normal LDL-C levels.
- Exclusion of lipid-lowering therapies and analysis of hepatic complication incidence rates (IDR) were performed.
Main Results:
- The HBL group exhibited a significantly higher incidence of hepatic complications compared to controls in both cohorts (IDR = 4.50 in CONSTANCES, IDR = 3.27 in UKBB).
- This increased risk was independent of established liver disease risk factors including obesity, alcohol, diabetes, and viral hepatitis.
- Sensitivity analyses using apolipoprotein-B or genetic definitions of HBL confirmed the findings.
Conclusions:
- Primary hypobetalipoproteinemia (HBL) is associated with a substantially elevated risk of hepatic complications.
- HBL should be recognized as a significant, independent risk factor for liver diseases.
- Specific prevention and screening strategies for liver disease in HBL patients warrant consideration.
Background & Aims:
Beyond cardiovascular disease protection, the health consequences of very low concentrations of low-density lipoprotein-cholesterol (LDL-C) remain a matter of debate. In primary hypobetalipoproteinemia (HBL), liver steatosis and cirrhosis have occasionally been reported. Here, we aimed to investigate the association between HBL and the risk of hepatic complications (cirrhosis complications and/or primary liver cancer) in the general population.
Methods:
A cohort study was conducted in the French population-based cohort CONSTANCES. Participants with primary HBL (LDL-C <5th percentile for age and sex, [HBL]) were compared with those with normal LDL-C concentrations (40th-60th percentile, [Control]). Participants on lipid-lowering therapies were excluded. For hepatic complications, follow-up events were compared by calculating the incidence density ratio (IDR). The same analyses were replicated in the UK Biobank (UKBB) cohort.
Results:
In the CONSTANCES and UKBB cohorts, 34,653 and 94,666 patients were analyzed, with median ages of 45 and 56 years, mean LDL-C concentrations (HBL vs. control) of 71 vs. 128 mg/dl and 86 vs. 142 mg/dl, and mean follow-up durations of 5.0 and 11.5 years, respectively. The HBL group presented a higher incidence of hepatic complications than the control group: 0.32/ vs. 0.07/1,000 person-years (IDR = 4.50, 95% CI 1.91-10.6) in CONSTANCES, and 0.69/ vs. 0.21/1,000 person-years (IDR = 3.27, 95% CI 2.63-4.06) in the UKBB. This risk proved to be independent of classic risk factors for liver disease (obesity, alcohol consumption, diabetes, viral hepatitis), including in a 5-year landmark analysis excluding early events. Sensitivity analyses based on apoliprotein-B levels (instead of LDL-C levels) or genetically defined HBL showed similar results.
Conclusions:
HBL is associated with a markedly increased risk of hepatic complications. HBL must be considered as a substantial independent risk factor for liver diseases which justifies specific prevention and screening.
Impact And Implications:
Hypobetalipoproteinemia (HBL) is a lipid disorder characterized by permanent, inherited low levels (below the 5th percentile) of low-density lipoprotein-cholesterol. While HBL is associated with a lower risk of cardiovascular events, some studies suggest that it may be associated with a potential risk of hepatic steatosis and hepatic complications. Here, we studied the association between HBL and hepatic complications (defined as cirrhosis complications and/or primary liver cancer) in two populations of several hundred thousand people, both in France (CONSTANCES cohort) and the United Kingdom (UKBB). The results show that HBL is associated with a significant and independent excess risk of hepatic complications, including primary liver cancer. Thus, in people with HBL, the value of regular liver monitoring must be studied.
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