Program in Translational NeuroPsychiatric Genomics
Program in Translational NeuroPsychiatric Genomics
News Article | November 10, 2016
Boston, MA - Women have a two-fold higher risk of developing Alzheimer's disease than men, yet strikingly little is known about how changes in brain function promote this difference -- and how early in midlife those changes can be detected. Now, in a population-based study involving more than 200 healthy women and men ages 47 to 55, a team of researchers led by the Brigham and Women's Hospital reveals specific changes in memory function that correspond to sex and menopausal stage, rather than chronological age. The work implicates key areas of the brain that are vulnerable to age-related decline and highlights the importance of ovarian hormones in maintaining memory function. The new study appears in the Nov. 9 online issue of the journal Menopause. "For years, the dominant thinking in the field was that women were at higher risk of Alzheimer's disease simply because they tend to live longer," said senior author Jill Goldstein, PhD, Director of Research at the Connors Center for Women's Health and Gender Biology at BWH. "But that idea was perpetuated by research that looked late in life -- not at middle age, when key hormonal transitions take place and when changes in memory begin to surface." Age-related cognitive decline impacts both men and women, with people reporting forgetfulness and a lack of mental clarity (so-called "brain fog") as they age. While women in general tend to fare better than men on tests of verbal memory and men have a higher rate of mild cognitive impairment later in life, women are disproportionately affected by Alzheimer's disease. In the U.S. alone, there are roughly 5.4 million people living with Alzheimer's disease; nearly two-thirds are women. Goldstein and her colleagues seized an opportunity to examine how and why these sex differences unfold when one of their long-studied community cohorts, known as the New England Family Study, began entering their later-40s and 50s. That allowed the researchers to carefully examine what happens to memory function in healthy, middle-age women over time as menopause unfolds -- spanning the pre- , peri-, and post-menopausal periods -- and to compare those findings to healthy, age-matched men. Because the individuals studied showed no signs of dementia or obvious memory loss, standard tests of memory function were not challenging enough to detect changes. So the team turned to a series of neuropsychological tests, refined by Dorene Rentz, PsyD, a lead author on the paper, senior neuropsychologist in the Department of Neurology at BWH, and an expert on Alzheimer's disease. These tests rigorously evaluate different forms of learning and memory, offering a finer-grained view that could identify even early, age-related cognitive deficits. The researchers found that, when compared to age-matched men, the women scored significantly higher on all categories of memory function assessed by the tests, with one notable exception: Post-menopausal women performed at roughly the same level as their male counterparts (and worse than the other women) on tests of initial learning and retrieval of information. The finding suggested changes in frontal areas of the brain, known for their roles in short-term memory and so-called "executive functions" -- advanced cognitive abilities, like organizing, structuring and evaluating information. In addition, hormone measurements revealed that across all women studied, higher estradiol levels (the form of estrogen that has the greatest effects on the brain) correlated with better memory performance. When taken together with other recent work, both from Goldstein's group and others, the Menopause paper helps paint a picture of the memory circuits in the brain that begin to change with age -- in both males and females -- and underscores the importance of steroid hormones, especially estradiol for women, in maintaining memory function. "We need to develop the capability to identify early on who is at highest risk of developing Alzheimer's disease," said Goldstein. "This is critical because the treatments given after disease onset have been unsuccessful. We hope findings from our cohort will ultimately provide clues early in mid-life with regard to who is at highest risk for the disease in later mid-life, and how this may differ for men and women. " Goldstein and her colleagues are already working toward that goal. Together with collaborator Philip de Jager, MD, PhD, who directs the Program in Translational NeuroPsychiatric Genomics at the Ann Romney Center for Neurologic Diseases at BWH, the researchers are designing a clinical risk tool that can help pinpoint patients who are most vulnerable to Alzheimer's disease. This tool -- which is being developed for both men and women -- will incorporate genetic risk factors as well as a host of other clinical characteristics known to affect memory decline and the sex differences therein. "Alzheimer's disease is one of the greatest public health challenges of our time," said Goldstein. "Going forward, it is imperative that we understand how to retain memory function throughout life, and that we incorporate these sex differences into future research and therapeutic discovery strategies." This study was supported by the National Institute of Mental Health (R01MH090291 to J. Goldstein). Additional support was provided by ORWH-NICHD BIRCWH K12 HD051959 to author E. Jacobs. The Harvard Clinical and Translational Science Center (NIH UL1RR025758) also provided support for serologic acquisition and evaluations. Brigham and Women's Hospital (BWH) is a 793-bed nonprofit teaching affiliate of Harvard Medical School and a founding member of Partners HealthCare. BWH has more than 4.2 million annual patient visits and nearly 46,000 inpatient stays, is the largest birthing center in Massachusetts and employs nearly 16,000 people. The Brigham's medical preeminence dates back to 1832, and today that rich history in clinical care is coupled with its national leadership in patient care, quality improvement and patient safety initiatives, and its dedication to research, innovation, community engagement and educating and training the next generation of health care professionals. Through investigation and discovery conducted at its Brigham Research Institute (BRI), BWH is an international leader in basic, clinical and translational research on human diseases, more than 3,000 researchers, including physician-investigators and renowned biomedical scientists and faculty supported by nearly $666 million in funding. For the last 25 years, BWH ranked second in research funding from the National Institutes of Health (NIH) among independent hospitals. BWH is also home to major landmark epidemiologic population studies, including the Nurses' and Physicians' Health Studies and the Women's Health Initiative as well as the TIMI Study Group, one of the premier cardiovascular clinical trials groups. For more information, resources and to follow us on social media, please visit BWH's online newsroom.
Shulman J.M.,Baylor College of Medicine |
Shulman J.M.,The Texas Institute |
Imboywa S.,Program in Translational NeuroPsychiatric Genomics |
Imboywa S.,Brigham and Women's Hospital |
And 29 more authors.
Human Molecular Genetics | Year: 2014
Using a Drosophila model of Alzheimer's disease (AD), we systematically evaluated 67 candidate genes based on AD-associated genomic loci (P < 10-4) from published human genome-wide association studies (GWAS). Genetic manipulation of 87 homologous fly genes was tested for modulation of neurotoxicity caused by human Tau, which forms neurofibrillary tangle pathology in AD. RNA interference (RNAi) targeting 9 genes enhanced Tau neurotoxicity, and in most cases reciprocal activation of gene expression suppressed Tau toxicity. Our screen implicates cindr, the fly ortholog of the human CD2AP AD susceptibility gene, as a modulator of Tau-mediated disease mechanisms. Importantly, we also identify the fly orthologs of FERMT2 and CELF1 as Tau modifiers, and these loci have been independently validated as AD susceptibility loci in the latest GWAS meta-analysis. Both CD2AP and FERMT2 have been previously implicated with roles in cell adhesion, and our screen additionally identifies a fly homolog of the human integrin adhesion receptors, ITGAM and ITGA9, as a modifier of Tau neurotoxicity. Our results highlight cell adhesion pathways as important in Tau toxicity and AD susceptibility and demonstrate the power of model organism genetic screens for the functional follow-up of human GWAS. © The Author 2013. Published by Oxford University Press. All rights reserved.