Researchers have found genetic overlap between Alzheimer's disease (AD) and two significant cardiovascular disease risk factors: high levels of inflammatory C-reactive protein (CRP) and plasma lipids or fats. The findings, based upon genome-wide association studies involving hundreds of thousands of individuals, suggest the two cardiovascular phenotypes play a role in AD risk - and perhaps offer a new avenue for potentially delaying disease progression.
The researchers used summary statistics from genome-wide association studies of more than 200,000 individuals, looking for overlap in single nucleotide polymorphisms (SNPs) associated with clinically diagnosed AD and CRP and the three components of total cholesterol: high-density lipoprotein (HDL), low-density lipoprotein (LDL) and triglycerides (TG). SNPs are fragments of DNA sequence that commonly vary among individuals within a population.
They found up to a 50-fold enrichment of AD SNPs for different levels of association with CRP, LDL, HDL and TG, which then lead to identification of 55 loci - specific locations on a gene, DNA sequence or chromosome - linked to increased AD risk.
The researchers next conducted a meta-analysis of these 55 variants across four independent AD study cohorts, encompassing almost 145,000 persons with AD and healthy controls, revealing two genome-wide significant variants on chromosomes 4 and 10. The two identified genes - HS3ST1 and ECHDC3 - were not previously associated with AD risk.
"Our findings indicate that a subset of genes involved with elevated plasma lipid levels and inflammation may also increase the risk for developing AD. Elevated levels of plasma lipids and inflammation can be modified with treatment, which means it could be possible to identify and therapeutically target individuals at increased risk for developing cardiovascular disease who are also at risk for developing Alzheimer's disease," said Rahul S. Desikan, MD, PhD, research fellow and radiology resident at the UC San Diego School of Medicine and the study's first author.
If so, the research may have significant ramifications. Late-onset AD is the most common form of dementia, affecting an estimated 30 million persons worldwide - a number that is expected to quadruple over the next 40 years. The societal costs, from medical to lost productivity, are staggering. The 2010 World Alzheimer Report estimated total annual costs at $606 billion.
The findings are published in current online issue of Circulation.
Co-authors include Linda K. McEvoy, and David S. Karow, UCSD Department of Radiology; Andrew J. Schork, UCSD Department of Cognitive Science; Yunpeng Wang, UCSD Department of Neurosciences and NORMENT and University of Oslo; Wesley K. Thompson, UCSD Department of Psychiatry; Abbas Dehghan, M. Arfan Ikram, and Sven J. van der Lee, Erasmus Medical Center, Netherlands; Daniel I. Chasman, Brigham and Women's Hospital; Dominic Holland, UCSD Department of Neurosciences; Chi-Hua Chen, UCSD Department of Radiology and NORMENT; James B. Brewer, UCSD departments of Radiology and Neurosciences; Christopher P. Hess, UCSF; Julie Williams, Rebecca Sims, and Michael C. O'Donovan, Cardiff University School of Medicine, UK; Seung Hoan Choi, Boston University; Joshua C. Bis, and Cornelia M. van Duijn, University of Washington; Vilmundur Gudnason, and Anita L.DeStefano, University of Iceland; Bruce M. Psaty, NHLBI; Lenore Launer, NIA; Sudha Seshadri, NHLBI and Boston University School of Medicine; Margaret A. Pericak-Vance, University of Miami; Richard Mayeux, Columbia University; Jonathan L. Haines, Case Western University; Lindsay A. Farrer, Boston University Schools of Medicine and Public Health; John Hardy, University College London; Ingun Dina Ulstein and Dag Aarsland, Oslo University Hospital; Tormod Fladby, University of Oslo; Linda R. White, and Sigrid B. Sando, Norwegian University of Science and Technology and Trondheim University Hospital; Arvid Rongve, Haugesund Hospital; Aree Witoelar, NORMENT; Srdjan Djurovic, University of Bergen, Norway; Bradley T. Hyman, Massachusetts General Hospital; Jon Snaedal, University Hospital Reykjavik; Stacy Steinberg, and Hreinn Stefansson, deCODE Genetics; Kari Stefansson, deCODE Genetics and University of Iceland; and Gerard D. Schellenberg, University of Pennsylvania. Funding for this research came, in part, from the National Institutes of Health (K02 NS067427; T32 EB005970; R01GM104400-01A; R01MH100351; AG033193 and U0149505), the Research Council of Norway, the South East Norway Health Authority, Norwegian Health Association and the KG Jebsen Foundation.