Relation between plasma and brain lipids

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Standard

Relation between plasma and brain lipids. / Wellington, Cheryl L; Frikke-Schmidt, Ruth.

I: Current Opinion in Lipidology, Bind 27, Nr. 3, 06.2016, s. 225-232.

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Harvard

Wellington, CL & Frikke-Schmidt, R 2016, 'Relation between plasma and brain lipids', Current Opinion in Lipidology, bind 27, nr. 3, s. 225-232. https://doi.org/10.1097/MOL.0000000000000291

APA

Wellington, C. L., & Frikke-Schmidt, R. (2016). Relation between plasma and brain lipids. Current Opinion in Lipidology, 27(3), 225-232. https://doi.org/10.1097/MOL.0000000000000291

Vancouver

Wellington CL, Frikke-Schmidt R. Relation between plasma and brain lipids. Current Opinion in Lipidology. 2016 jun.;27(3):225-232. https://doi.org/10.1097/MOL.0000000000000291

Author

Wellington, Cheryl L ; Frikke-Schmidt, Ruth. / Relation between plasma and brain lipids. I: Current Opinion in Lipidology. 2016 ; Bind 27, Nr. 3. s. 225-232.

Bibtex

@article{6f568ed9e7564b6ca553bba3b21b1bb5,
title = "Relation between plasma and brain lipids",
abstract = "PURPOSE OF REVIEW: This article evaluates recent experimental and human evidence regarding the involvement of lipids, lipoproteins, and apolipoproteins in neurodegenerative diseases, and reviews the current literature of the effects of cholesterol-lowering treatment on cognition.RECENT FINDINGS: Plasma levels of traditional lipids and lipoproteins are not consistently associated with risk of dementia even though low plasma levels of apolipoprotein E, through unknown mechanisms, robustly predict future dementia. Experimental evidence suggests neuroprotective roles of several brain and cerebrospinal fluid apolipoproteins. Whether plasma levels of apolipoprotein E, or any other apolipoprotein with possible central nervous system and/or blood-brain barrier functions (apolipoproteins J, A-I, A-II, A-IV, D, C-I, and C-III) may become accessible biomarker components that improve risk prediction for dementia together with genetic risk variants and cardiovascular risk factors remains to be determined.SUMMARY: Apolipoproteins with well established functions in peripheral lipid metabolism may play important roles for brain vascular health and Alzheimer's disease pathophysiology. Experimental work on lipids, lipoproteins, and apolipoproteins in the central nervous system together with robust prospective human studies will help to substantiate the drug target potential of these lipid components.",
keywords = "Journal Article",
author = "Wellington, {Cheryl L} and Ruth Frikke-Schmidt",
year = "2016",
month = jun,
doi = "10.1097/MOL.0000000000000291",
language = "English",
volume = "27",
pages = "225--232",
journal = "Current Opinion in Lipidology",
issn = "0957-9672",
publisher = "Lippincott Williams & Wilkins, Ltd.",
number = "3",

}

RIS

TY - JOUR

T1 - Relation between plasma and brain lipids

AU - Wellington, Cheryl L

AU - Frikke-Schmidt, Ruth

PY - 2016/6

Y1 - 2016/6

N2 - PURPOSE OF REVIEW: This article evaluates recent experimental and human evidence regarding the involvement of lipids, lipoproteins, and apolipoproteins in neurodegenerative diseases, and reviews the current literature of the effects of cholesterol-lowering treatment on cognition.RECENT FINDINGS: Plasma levels of traditional lipids and lipoproteins are not consistently associated with risk of dementia even though low plasma levels of apolipoprotein E, through unknown mechanisms, robustly predict future dementia. Experimental evidence suggests neuroprotective roles of several brain and cerebrospinal fluid apolipoproteins. Whether plasma levels of apolipoprotein E, or any other apolipoprotein with possible central nervous system and/or blood-brain barrier functions (apolipoproteins J, A-I, A-II, A-IV, D, C-I, and C-III) may become accessible biomarker components that improve risk prediction for dementia together with genetic risk variants and cardiovascular risk factors remains to be determined.SUMMARY: Apolipoproteins with well established functions in peripheral lipid metabolism may play important roles for brain vascular health and Alzheimer's disease pathophysiology. Experimental work on lipids, lipoproteins, and apolipoproteins in the central nervous system together with robust prospective human studies will help to substantiate the drug target potential of these lipid components.

AB - PURPOSE OF REVIEW: This article evaluates recent experimental and human evidence regarding the involvement of lipids, lipoproteins, and apolipoproteins in neurodegenerative diseases, and reviews the current literature of the effects of cholesterol-lowering treatment on cognition.RECENT FINDINGS: Plasma levels of traditional lipids and lipoproteins are not consistently associated with risk of dementia even though low plasma levels of apolipoprotein E, through unknown mechanisms, robustly predict future dementia. Experimental evidence suggests neuroprotective roles of several brain and cerebrospinal fluid apolipoproteins. Whether plasma levels of apolipoprotein E, or any other apolipoprotein with possible central nervous system and/or blood-brain barrier functions (apolipoproteins J, A-I, A-II, A-IV, D, C-I, and C-III) may become accessible biomarker components that improve risk prediction for dementia together with genetic risk variants and cardiovascular risk factors remains to be determined.SUMMARY: Apolipoproteins with well established functions in peripheral lipid metabolism may play important roles for brain vascular health and Alzheimer's disease pathophysiology. Experimental work on lipids, lipoproteins, and apolipoproteins in the central nervous system together with robust prospective human studies will help to substantiate the drug target potential of these lipid components.

KW - Journal Article

U2 - 10.1097/MOL.0000000000000291

DO - 10.1097/MOL.0000000000000291

M3 - Review

C2 - 27149391

VL - 27

SP - 225

EP - 232

JO - Current Opinion in Lipidology

JF - Current Opinion in Lipidology

SN - 0957-9672

IS - 3

ER -

ID: 174860893