Lung For-Wey, Kao Wei-Tsung, Shu Bih-Ching, Yen Yung-Chieh, Tzeng Dong-Sheng
Department of Psychiatry, Military Kaohsiung General Hospital, Kaohsiung, Taiwan.
Hum Hered. 2006;62(3):135-44. doi: 10.1159/000096417. Epub 2006 Oct 20.
Establish a possible conceptual relationship among Apo E and PLA2 polymorphism and lipid profiles.
Five hundred subjects aged 65 to 74 years were randomly selected from a community in southern Taiwan to assess the relationship between Apo E and PLA2 polymorphisms and lipid profiles. Two hundred fifty-six participants agreed to have venous blood drawn for DNA studies.
By multiple linear regression, the PLA2 A2 allele showed a statistically significant influence on LDL-C (p = 0.0097), and the Apo epsilon2 allele showed a statistically significant influence on HDL-C (p = 0.0004), however, the interaction between the PLA2 A2 allele and the Apo epsilon2 allele was found to be significant in the blood fraction of HDL-C (p = 0.0388) and LDL-C (p = 0.0002). Decreasing HDL-C and increasing LDL-C were found when the PLA2 A2 and Apo epsilon2 allele co-existed.
The presence of a physiologic balance contributes significantly to homeostatic and compensatory responses regulating blood HDL-C and LDL-C profiles. A module map of the generation-control cycle and conditional activity among Apo E, PLA2, and lipid levels is presented, and both behaviours and biological perspectives under the consilience model may suggest a new approach to many kinds of complex disorders.
