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Apolipoprotein-E Gene Polymorphism and Lipid Composition among IUGR and AGA Neonates
Bharathi Elangovan1, Rajesh N T1, Meenu Subrahmanian2
1Department of Pediatrics, PSG Institute of Medical Sciences & Research, Coimbatore, Tamil Nadu, India.
Insights
The apolipoprotein E (APOE) ε4 allele, linked to adult metabolic diseases, was less frequent in intrauterine growth restriction (IUGR) neonates. However, neonates with the APOE ε4 allele exhibited abnormal lipid profiles, suggesting a potential association.
Area of Science:
- Genetics and Molecular Biology
- Neonatal Medicine
- Metabolic Disorders
Background:
- Intrauterine growth restriction (IUGR) is associated with altered neonatal outcomes.
- Apolipoprotein E (APOE) gene polymorphism influences lipid metabolism and is linked to adult metabolic diseases.
- The role of APOE gene variants in neonates, particularly those with IUGR, requires further investigation.
Purpose of the Study:
- To investigate the association between APOE gene polymorphism (ε2, ε3, ε4 alleles) and lipid profiles in IUGR neonates compared to appropriate for gestational age (AGA) neonates.
- To determine the allelic frequencies of APOE isoforms in IUGR and AGA neonates.
- To analyze the relationship between APOE genotype and lipid parameters (Total Cholesterol, LDL, HDL, Triglycerides) in both groups.
Main Methods:
- Observational study conducted in a South Indian teaching hospital's neonatal unit.
- Genomic DNA was extracted from peripheral venous blood samples of 102 IUGR and AGA neonates.
- APOE rs429358 and rs7412 genotyping was performed using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). Lipid profiles were analyzed from pre-feed blood samples.
Main Results:
- The frequency of the APOE ε4 allele was lower in IUGR neonates (6.7%) compared to AGA neonates (17.6%).
- The APOE ε2 allele was the second most predominant isoform in the study population.
- Neonates carrying the APOE ε4 allele showed elevated mean Total Cholesterol and Triglyceride levels in both IUGR and AGA groups, although not statistically significant (p > 0.05).
Conclusions:
- The APOE ε4 allele, a risk factor for adult metabolic diseases, was found less frequently among IUGR neonates in this cohort.
- Despite lower frequency, the presence of the APOE ε4 allele was associated with abnormal lipid profiles in both IUGR and AGA neonates, suggesting a potential early-life impact.
- Further research is warranted to elucidate the long-term implications of APOE genotype on lipid metabolism and health outcomes in individuals born with IUGR.
Abstract:
Objective The objective of this study is to study the profile of apolipoprotein E ( APOE ) gene polymorphism and lipid profile among intrauterine growth restriction (IUGR) and appropriate for gestational age (AGA) neonates. This is an observational study. This study was done at the neonatal unit of a teaching hospital in South India. All consecutively born IUGR neonates (cases) of more than 32 weeks' gestational age and AGA neonates (controls) were enrolled for the study. Genomic DNA extraction was done from a total of 102 peripheral venous blood samples. Genotyping of the APOE rs429358 and rs7412 defining the ε2, ε3, and ε4 alleles was done by polymerase chain reaction-restriction fragment length polymorphism method. Prefeed venous blood was collected and analyzed for lipid profile estimation. The allelic frequencies of cases versus control were ε2-9 (8.7%) versus 3 (2.9%); ε3-88 (84.6%) versus 81 (79.4%); and ε4-7 (6.7%) versus 18 (17.6%). The frequency of ε4 isoform allele, associated with adult onset of metabolic diseases was less among the IUGR group. The mean total cholesterol (TC), Low-Density Lipoprotein (LDL), High-Density Lipoprotein, and triglyceride (TG) were 107.59 ± 35.99, 51.69 ± 24.68, 21.75 ± 9.58, and 151.22 ± 61.84 mg/dL, respectively, in the IUGR group. The mean TC and LDL levels in IUGR group were marginally higher than AGA neonates (107 ± 35.99 vs. 100.37 ± 22.69 mg/dL and 51.69 ± 24.68 versus 46.9 ± 19.51 mg/dL, p > 0.05). In both groups, the mean TC and TGL levels were elevated in the ε4 isoform subgroup ( p > 0.05). In our study, the ε2 allele was the second most predominant APOE isoform and the ε4 allele of the APOE gene associated with adult-onset diseases was not increased among IUGR neonates. Neonates with ε4 allele showed an abnormal lipid profile in both study groups suggesting a possible association.
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