Key result
Newborns carrying at least one 5D allele (n=27) had a significantly higher frequency of being in the upper tertile for left ventricular mass indices compared to those with the 5I/5I genotype (n=135).
Why the study?
The PPP3R1 rs3039851 polymorphism is associated with left ventricular hypertrophy in hypertensive patients and athletes, but its association with left ventricular mass in full-term healthy newborns was unknown.
Is the PPP3R1:rs3039851 polymorphism associated with left ventricular mass in healthy full-term newborns?
Cross-Sectional (n=162)
Is the PPP3R1:rs3039851 polymorphism associated with left ventricular mass in healthy full-term newborns?
The PPP3R1:rs3039851 polymorphism may contribute to subtle variations in left ventricular mass at birth in healthy newborns.
Subtle LVM variation linked to PPP3R1 variant in newborns warrants no clinical action; leaves open its role in early cardiac development.
Background: The five base-pair (bp) insertion/deletion (rs3039851) polymorphism in the PPP3R1 gene, which encodes calcineurin subunit B type 1, has been found to be associated with left ventricular hypertrophy (LVH) in hypertensive patients and in athletes. The aim of this study is to analyze the possible association between PPP3R1:rs3039851 polymorphism and left ventricular mass (LVM) in full-term healthy newborns. Methods: The study group consisted of 162 consecutive, full-term, healthy newborns. Two-dimensional M-mode echocardiography was used to assess LVM. The PPP3R1:rs3039851 polymorphism was identified by PCR-RFLP in genomic DNA extracted from cord blood leukocytes. Results: No significant differences were found between newborns homozygous for the reference allele (5I/5I, n = 135) and newborns carrying at least one 5D allele (n = 27) for LVM standardized for body mass, body length or body surface area (LVM/BM, LVM/BL or LVM/BSA, respectively). However, the frequency of PPP3R1:rs3039851 genotypes with a 5D allele (5I/5D + 5D/5D) among newborns with the largest LVM/BM or LVM/BSA (upper tertile) was statistically significantly higher compared with the prevalence in individuals with the lowest values of both indices (lower tertile). Conclusions: Our results suggest that the PPP3R1:rs3039851 polymorphism may contribute to subtle variation in left ventricular mass at birth.
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Gorący et al. (2023) conducted a cross-sectional in Healthy newborns (n=162). PPP3R1:rs3039851 polymorphism (5D allele) vs. Homozygous for the reference allele (5I/5I) was evaluated on Left ventricular mass (LVM) standardized for body mass, body length or body surface area. Newborns carrying at least one 5D allele (n=27) had a significantly higher frequency of being in the upper tertile for left ventricular mass indices compared to those with the 5I/5I genotype (n=135).
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