Alternations of Lipoprotein Profiles in the Plasma as Biomarkers of Huntington's Disease

Cells. 2023 Jan 20;12(3):385. doi: 10.3390/cells12030385.

Abstract

Alterations in lipid composition and disturbed lipoprotein metabolism are involved in the pathomechanism of Huntington's disease (HD). Here, we measured 112 lipoprotein subfractions and components in the plasma of 20 normal controls, 24 symptomatic (sympHD) and 9 presymptomatic (preHD) HD patients. Significant changes were found in 30 lipoprotein subfractions and components in all HD patients. Plasma levels of total cholesterol (CH), apolipoprotein (Apo)B, ApoB-particle number (PN), and components of low-density lipoprotein (LDL) were lower in preHD and sympHD patients. Components of LDL4, LDL5, LDL6 and high-density lipoprotein (HDL)4 demonstrated lower levels in preHD and sympHD patients compared with controls. Components in LDL3 displayed lower levels in sympHD compared with the controls, whereas components in very low-density lipoprotein (VLDL)5 were higher in sympHD patients compared to the controls. The levels of components in HDL4 and VLDL5 demonstrated correlation with the scores of motor assessment, independence scale or functional capacity of Unified Huntington's Disease Rating Scale. These findings indicate the potential of components of VLDL5, LDL3, LDL4, LDL5 and HDL4 to serve as the biomarkers for HD diagnosis and disease progression, and demonstrate substantial evidence of the involvement of lipids and apolipoproteins in HD pathogenesis.

Keywords: Huntington’s disease; biomarker; high-density lipoprotein; lipoprotein; low-density lipoprotein; very low-density lipoprotein.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apolipoproteins B
  • Biomarkers
  • Humans
  • Huntington Disease* / diagnosis
  • Lipoproteins
  • Lipoproteins, LDL / metabolism
  • Triglycerides

Substances

  • Triglycerides
  • Lipoproteins
  • Lipoproteins, LDL
  • Apolipoproteins B
  • Biomarkers

Grants and funding

C.-M. Chen (CMRPG3L141 from Chang Gung Medical Foundation); M.-L. Cheng (CMRPD1H0512 from Chang Gung Medical Foundation and EMRPD1M0421 from Ministry of Education (MOE) in Taiwan.