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1.
Nat Med ; 20(4): 415-8, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24608097

ABSTRACT

Alzheimer's disease causes a progressive dementia that currently affects over 35 million individuals worldwide and is expected to affect 115 million by 2050 (ref. 1). There are no cures or disease-modifying therapies, and this may be due to our inability to detect the disease before it has progressed to produce evident memory loss and functional decline. Biomarkers of preclinical disease will be critical to the development of disease-modifying or even preventative therapies. Unfortunately, current biomarkers for early disease, including cerebrospinal fluid tau and amyloid-ß levels, structural and functional magnetic resonance imaging and the recent use of brain amyloid imaging or inflammaging, are limited because they are either invasive, time-consuming or expensive. Blood-based biomarkers may be a more attractive option, but none can currently detect preclinical Alzheimer's disease with the required sensitivity and specificity. Herein, we describe our lipidomic approach to detecting preclinical Alzheimer's disease in a group of cognitively normal older adults. We discovered and validated a set of ten lipids from peripheral blood that predicted phenoconversion to either amnestic mild cognitive impairment or Alzheimer's disease within a 2-3 year timeframe with over 90% accuracy. This biomarker panel, reflecting cell membrane integrity, may be sensitive to early neurodegeneration of preclinical Alzheimer's disease.


Subject(s)
Alzheimer Disease/blood , Cognitive Dysfunction/blood , Phospholipids/blood , Aged , Alzheimer Disease/complications , Alzheimer Disease/diagnosis , Asparagine/blood , Biomarkers , Carnitine/blood , Cognitive Dysfunction/complications , Cognitive Dysfunction/diagnosis , Cohort Studies , Dipeptides/blood , Female , Humans , Longitudinal Studies , Lysophosphatidylcholines/blood , Malates/blood , Male , Memory Disorders/blood , Memory Disorders/diagnosis , Memory Disorders/etiology , Metabolome , Neuropsychological Tests , Phosphatidylcholines/blood , Phosphatidylinositols/blood , Proline/blood , Prospective Studies , Sensitivity and Specificity , Sphingomyelins/blood , Ursodeoxycholic Acid/analogs & derivatives , Ursodeoxycholic Acid/blood
2.
J Clin Hypertens (Greenwich) ; 14(3): 178-83, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22372778

ABSTRACT

Over the past two years, the business community of Monroe County, which includes Rochester, New York, has been engaging in a collaborative to improve outcomes for people with high blood pressure. As the employers examined the costs of care in the community, they recognized two important factors. First, the costs of care for the uninsured, the underinsured, and the Medicare population influence the business community's cost of care. Second, trying to redesign care just for their employees alone was not effective. This project is unique in that the stimulus and funding for community-wide action comes from the business community. They saw beyond the often unsuccessful short-term cost reduction programs and joined with a community-focused organization, the Finger Lakes Health Systems Agency, to construct a multi-year, multi-faceted intervention designed to encourage practice redesign and an invigorated community commitment to partnership and accountability. This report describes the process to date and hopefully will stimulate conversations about mechanisms to encourage similar collaboration within other communities.


Subject(s)
Community Health Services , Hypertension/prevention & control , Patient Care/statistics & numerical data , Quality of Health Care/statistics & numerical data , Cooperative Behavior , Education , Health Promotion , Humans , Hypertension/diagnosis , Hypertension/epidemiology , Life Style , Motivation , New York/epidemiology , Patient Care/standards , Program Development , Program Evaluation , Quality of Health Care/standards , Registries , Social Marketing , Time Factors
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