TY - JOUR
T1 - Lipoprotein subfractions by ion mobility in lean and obese children
AU - Benson, Matthew
AU - Hossain, Jobayer
AU - Caulfield, Michael P.
AU - Damaso, Ligeia
AU - Gidding, Samuel
AU - Mauras, Nelly
PY - 2012/12
Y1 - 2012/12
N2 - Objective: To establish normative data for lipoprotein subfractions using a novel ion mobility assay in healthy lean children and to compare their data with those of obese children preselected with normal glucose, blood pressure, and relatively normal lipids. Study design: Fasting blood samples in 162 children aged 7.0-18.9 years (75 lean [body mass index: 18.6 ± 6.6 kg/m2] and 87 obese [body mass index: 31.7 ± 5.4 kg/m 2]) were analyzed. Correlation of lipoprotein subfractions with anthropometric and laboratory markers was performed. Principal component analysis was used to avoid using correlated variables. Results: Normative data for lipid subfractions were obtained in healthy children. Lean children had higher high-density lipoprotein (HDL)-large (76%), HDL-small (13%), and HDL-total (27%) compared with obese (P < .01), and lower low-density lipoprotein (LDL)-medium (-30%, P < .01) and medium + small (-21%, P = .02) as well as LDL-total (-13%, P = .035). In both groups, the LDL component was higher in males and pubertal children (P < .01). Prepubertal children had a higher HDL component than pubertal ones (P < .004). Adjusting for sex and pubertal status LDL component was positively, and HDL component negatively, correlated with obesity (P < .004). Conclusions: Despite relatively normal triglycerides and cholesterol measured with standard assays at screening, ion mobility analysis showed significant differences in lipid and apolipoprotein subfractions between lean and obese children, even those prepubertal. Long-term, prospective follow-up may better characterize the predictability of lipid subfractions for future cardiovascular disease risk in children.
AB - Objective: To establish normative data for lipoprotein subfractions using a novel ion mobility assay in healthy lean children and to compare their data with those of obese children preselected with normal glucose, blood pressure, and relatively normal lipids. Study design: Fasting blood samples in 162 children aged 7.0-18.9 years (75 lean [body mass index: 18.6 ± 6.6 kg/m2] and 87 obese [body mass index: 31.7 ± 5.4 kg/m 2]) were analyzed. Correlation of lipoprotein subfractions with anthropometric and laboratory markers was performed. Principal component analysis was used to avoid using correlated variables. Results: Normative data for lipid subfractions were obtained in healthy children. Lean children had higher high-density lipoprotein (HDL)-large (76%), HDL-small (13%), and HDL-total (27%) compared with obese (P < .01), and lower low-density lipoprotein (LDL)-medium (-30%, P < .01) and medium + small (-21%, P = .02) as well as LDL-total (-13%, P = .035). In both groups, the LDL component was higher in males and pubertal children (P < .01). Prepubertal children had a higher HDL component than pubertal ones (P < .004). Adjusting for sex and pubertal status LDL component was positively, and HDL component negatively, correlated with obesity (P < .004). Conclusions: Despite relatively normal triglycerides and cholesterol measured with standard assays at screening, ion mobility analysis showed significant differences in lipid and apolipoprotein subfractions between lean and obese children, even those prepubertal. Long-term, prospective follow-up may better characterize the predictability of lipid subfractions for future cardiovascular disease risk in children.
KW - Apo
KW - Apolipoprotein
KW - BMI
KW - Body mass index
KW - HDL
KW - HOMA
KW - High-density lipoprotein
KW - Highly sensitive C-reactive protein
KW - Homeostatic model assessment
KW - LDL
KW - LDL-VS
KW - Low-density lipoprotein
KW - Low-density lipoprotein-very small
KW - PC
KW - PCA
KW - Principal component
KW - Principal component analysis
KW - VLDL
KW - Very low density lipoprotein
KW - hs-CRP
UR - https://www.scopus.com/pages/publications/84869487734
U2 - 10.1016/j.jpeds.2012.05.060
DO - 10.1016/j.jpeds.2012.05.060
M3 - Article
C2 - 22819275
AN - SCOPUS:84869487734
SN - 0022-3476
VL - 161
SP - 997-1003.e1
JO - Journal of Pediatrics
JF - Journal of Pediatrics
IS - 6
ER -