Related Experiment Video
Updated: Jun 21, 2026

Isolation, Characterization, and Purification of Macrophages from Tissues Affected by Obesity-related Inflammation
Published on: April 3, 2017
Decrease of Lp(a) during weight reduction in obese children is modified by the apo(a) kringle-IV copy number
A Brandstätter1, A Lingenhel, K Zwiauer
1Division of Genetic Epidemiology, Department of Medical Genetics, Molecular and Clinical Pharmacology, Innsbruck Medical University, Schöpfstrasse, Innsbruck, Austria.
Insights
Weight reduction significantly lowers lipoprotein(a) [Lp(a)] levels in obese children. This effect is influenced by apolipoprotein(a) [apo(a)] variations, particularly in those with high initial Lp(a) concentrations.
Area of Science:
- Pediatric Endocrinology
- Cardiovascular Risk Factors
- Metabolic Syndrome
Background:
- Lipoprotein(a) [Lp(a)] is an independent cardiovascular disease risk factor.
- Lp(a) levels are primarily determined by kringle-IV repeat copy number variation (CNV) in the apolipoprotein(a) [apo(a)] gene locus.
Purpose of the Study:
- To investigate the immediate impact of weight reduction on plasma Lp(a) levels in obese children.
- To determine if this effect is dependent on apo(a) CNV.
Main Methods:
- A 3-week prospective longitudinal intervention study involving a low-fat hypocaloric diet in 140 obese children.
- Measurements included body weight, BMI, plasma Lp(a), lipids, apolipoproteins, insulin, and C-reactive protein before and after the intervention.
- Apo(a) kringle-IV repeat number was determined using gel electrophoresis.
Main Results:
- Mean weight loss was 5.0 kg (6.6% reduction in relative BMI).
- Plasma Lp(a) levels decreased by 19% (from 24.4 to 17.9 mg/dL, P<0.001).
- Lp(a) reduction was more pronounced in individuals with low molecular weight apo(a) phenotypes compared to high.
Conclusions:
- Weight reduction in obese children leads to significant decreases in Lp(a) levels.
- The magnitude of Lp(a) reduction is influenced by the apo(a) molecular phenotype and baseline Lp(a) concentrations.
Background:
Lipoprotein(a) [Lp(a)] is considered an independent risk factor for cardiovascular disease. Its concentration is mainly determined by the kringle-IV repeat copy number variation (CNV) at the apolipoprotein(a) [apo(a)] locus.
Objective:
We aimed to investigate the immediate effect of weight reduction on plasma Lp(a) levels and its dependency on the apo(a) CNV in obese children.
Design:
We performed a prospective longitudinal intervention study of a low-fat hypocaloric diet conducted in a 3-week dietary camp for obese children. In all, 140 obese participants (54 boys and 86 girls) with a mean age of 12.5+/-1.6 years and a mean relative body mass index (BMI) before treatment of 165.6+/-24.7% were included. Body weight and plasma levels of Lp(a), lipids, apolipoproteins A-I and B, insulin, and C-reactive protein were determined before the onset and after the end of the intervention. In addition, the number of apo(a) kringle-IV repeats were determined using sodium dodecyl sulfate agarose gel electrophoresis.
Results:
The mean loss of body weight was 5.0+/-1.3 kg (-6.6%), resulting in a mean decrease of the relative BMI of 6.6%. Blood chemistry revealed significant changes in all parameters, especially in Lp(a), with a decrease from 24.4+/-30.6 to 17.9+/-22.6 mg per 100 ml or -19% (P<0.001). The decrease of Lp(a) levels was higher in the group with low compared with high molecular weight apo(a) phenotypes (-23.9 vs -16.6%).
Conclusions:
Weight reduction in obese children is associated with significant changes in Lp(a) levels, especially in subjects with high pre-treatment Lp(a) concentrations. This effect is markedly influenced by the molecular phenotype at the copy-number variable apo(a) locus.
Related Concept Videos
Pharmacokinetics in Obese Patients: Drug Absorption and Distribution
Atherosclerosis III: Management
Pharmacokinetics in Obese Patients: Drug Metabolism and Excretion
Obesity
Drug Dosing: Obese Patients
Lipid Digestion
