Shunsuke Araki1, Shutaro Suga2, Fuyu Miyake2, Shun Ichikawa2, Tadamune Kinjo2, Yukiyo Yamamoto3, Koichi Kusuhara3. 1. Department of Pediatrics, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan; Center of Maternal, Fetal and Neonatal Medicine, University of Occupational and Environmental Health Hospital, Kitakyushu, Japan. Electronic address: arashun@med.uoeh-u.ac.jp. 2. Department of Pediatrics, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan; Center of Maternal, Fetal and Neonatal Medicine, University of Occupational and Environmental Health Hospital, Kitakyushu, Japan. 3. Department of Pediatrics, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.
Abstract
BACKGROUND AND AIMS: Protein convertase subtilisin/Kexin type-9 (PCSK9) is a substantial player in lipoprotein metabolism. This study was designed to elucidate the role of PCSK9 in the regulation of lipoprotein during the fetal period. STUDY DESIGN AND SUBJECTS: This study was a cross-sectional study. Eighty-one neonates (45 males, 36 females) who were admitted to the neonatal intensive care unit were enrolled in the study. The median age in gestational weeks and weight at birth were 37.1 weeks and 2493 g, respectively. There were no gender differences, but the proportion of infants who were small-for-gestational age (SGA) was significantly higher among females than males. The prefed serum PCSK9 level was assayed with ELISA kits. RESULTS: The median PCSK9 concentration in male newborns was significantly lower than that in females (148.2 ng/ml vs. 171.4 ng/ml, respectively, p<0.001). Circulating serum PCSK9 levels were positively correlated with total cholesterol (r=0.281, p<0.05) and low-density lipoprotein cholesterol (LDL-C; r=0.272, p<0.05). However, there were no correlations between PCSK9 levels and birth weight, gestational age or SGA. Multivariate forward stepwise linear regression analysis revealed that gestational age and circulating PCSK9 levels were independent predictors of the serum LDL-C levels in newborn infants. CONCLUSION: Our first quantitative analysis of neonatal serum PCSK9 levels at birth showed that circulating PCSK9 levels show gender-based differences and are significantly correlated with LDL-C. These results suggest that PCSK9 could play an important role in regulating LDL-C levels during the fetal period.
BACKGROUND AND AIMS: Protein convertase subtilisin/Kexin type-9 (PCSK9) is a substantial player in lipoprotein metabolism. This study was designed to elucidate the role of PCSK9 in the regulation of lipoprotein during the fetal period. STUDY DESIGN AND SUBJECTS: This study was a cross-sectional study. Eighty-one neonates (45 males, 36 females) who were admitted to the neonatal intensive care unit were enrolled in the study. The median age in gestational weeks and weight at birth were 37.1 weeks and 2493 g, respectively. There were no gender differences, but the proportion of infants who were small-for-gestational age (SGA) was significantly higher among females than males. The prefed serum PCSK9 level was assayed with ELISA kits. RESULTS: The median PCSK9 concentration in male newborns was significantly lower than that in females (148.2 ng/ml vs. 171.4 ng/ml, respectively, p<0.001). Circulating serum PCSK9 levels were positively correlated with total cholesterol (r=0.281, p<0.05) and low-density lipoprotein cholesterol (LDL-C; r=0.272, p<0.05). However, there were no correlations between PCSK9 levels and birth weight, gestational age or SGA. Multivariate forward stepwise linear regression analysis revealed that gestational age and circulating PCSK9 levels were independent predictors of the serum LDL-C levels in newborn infants. CONCLUSION: Our first quantitative analysis of neonatal serum PCSK9 levels at birth showed that circulating PCSK9 levels show gender-based differences and are significantly correlated with LDL-C. These results suggest that PCSK9 could play an important role in regulating LDL-C levels during the fetal period.
Authors: Sonia Nava-Salazar; Arturo Flores-Pliego; Giovanni Pérez-Martínez; Sandra Parra-Hernández; America Vanoye-Carlo; Francisco Ibarguengoitia-Ochoa; Otilia Perichart-Perera; Enrique Reyes-Muñoz; Juan Mario Solis-Paredes; Salvador Espino Y Sosa; Guadalupe Estrada-Gutierrez Journal: Reprod Sci Date: 2022-04-25 Impact factor: 3.060