Children 24 items
Studies
- A genome-wide significant signal near CETP is linked to doubled HDL cholesterol in youth with type 2 diabetes (J Endocr Soc 2021)
- CETP gene mutations shape LDL and HDL cholesterol from birth through the first year of life (Clin Chim Acta 2009)
- CETP TaqIB B2 allele linked to higher HDL cholesterol in Greek children (Nutr Metab Cardiovasc Dis 2010)
- CETP D442G mutation raises HDL cholesterol in Vietnamese schoolgirls regardless of nutritional status (Pediatr Res 2005)
- CETP TaqIB and apoE genotypes interact to shape cholesterol levels in 7-year-old children (Nutr Metab Cardiovasc Dis 2002)
- Serum CETP is roughly double in obese children and falls with weight-loss therapy (Obes Res 2002)
- CETP B1B1 genotype tracks with lower HDL cholesterol from birth through age 5-6 in children at cardiovascular risk (Med Sci Monit 2013)
- Low serum albumin is the main driver of elevated CETP in children with active nephrotic syndrome (Clin Biochem 2007)
- The CETP D442G mutation raises HDL cholesterol in adults but not children, first pediatric study of this variant finds (Pediatr Res 2001)
- Increased CETP activity tracks with the atherogenic lipoprotein profile of obese children (Atherosclerosis 1997)
- CETP activity exceeds that of adults and control children in kids on peritoneal dialysis for end-stage renal disease (Nephron 1996)
- Children with obesity show reduced CETP activity alongside broader HDL antioxidant breakdown and higher oxidative stress (J Clin Lipidol 2026)
- Largest paediatric lipid GWAS to date confirms CETP as a robust HDL locus in Indian schoolchildren, with rare CETP variants also implicated (J Hum Genet 2025)
- CETP gene variants help explain HDL cholesterol levels in children with sickle cell disease (Braz J Med Biol Res 2024)
- A high triglyceride to HDL cholesterol ratio predicts elevated CETP activity in children (Indian J Pediatr 2021)
- Low CETP activity late in pregnancy, in mother and placenta alike, is linked to giving birth to small-for-gestational-age infants (Sci Rep 2021)
- CETP variants A373P and Taq1 have opposite effects on low HDL cholesterol risk in Iranian children and teenagers (Atherosclerosis 2014)
- CETP variant rs708272 associates with HDL-C and LDL-C levels in 365 Turkish children (OMICS 2013)
- Three CETP variants are among only six SNPs linked to HDL cholesterol in European adolescents, first shown in this age group (Atherosclerosis 2011)
- Olive-oil-enriched skim milk raises HDL cholesterol most in children with the CETP B1B1 genotype (Ann Nutr Metab 2010)
- CETP variant rs708272 ranks among the top ten SNPs in a 24-gene model predicting childhood and adolescent obesity, alongside diet and gut microbiota (Sci Rep 2020)
- Serum CETP is lowest at birth and rises sharply to peak levels in infancy, reference data from healthy Chinese children (Clin Biochem 2008)
- CETP D442G mutation is found in two families with Lowe syndrome and elevated HDL cholesterol (Acta Paediatr 1997)
- CETP levels track with bile acid concentration in children with Alagille syndrome cholestasis (Atherosclerosis 2008)