{"id":213160,"date":"2017-08-25T03:41:07","date_gmt":"2017-08-25T07:41:07","guid":{"rendered":"http:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/forget-me-not-triad-city-beat\/"},"modified":"2017-08-25T03:41:07","modified_gmt":"2017-08-25T07:41:07","slug":"forget-me-not-triad-city-beat","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/human-genetics\/forget-me-not-triad-city-beat\/","title":{"rendered":"Forget me not &#8211; Triad City Beat"},"content":{"rendered":"<p><p>    The community room looks like the interior of any    well-appointed modern house from Starmount to Summerfield, with    ocean-blue walls, mahogany-style tables matched with    high-backed chairs, a sleek metallic refrigerator and    comfortable couches.  <\/p>\n<p>    Theres one key difference: The dining room, kitchen, living    area and bathroom are collapsed into one large room with no    dividers. Located on the third floor of a repurposed textile    building across the street from Revolution Mill, the community    room at the Center for Outreach in Alzheimers, Age and    Community Health, or COAACH, functions as a classroom for    families learning how to take care of a loved one developing    Alzheimers disease or dementia.  <\/p>\n<p>    The team wanted it to look like a home, said Donna Bradby, a    publicist at NC A&T University, so you could cook a    healthy meal, sit your loved one down at the table and then do    things like transferring them to the bathroom and helping them    brush their teeth.  <\/p>\n<p>    Bradby gestured toward the full-length mirror at the end of the    room.  <\/p>\n<p>    My aunt, Annie Ruth Ingram, had Alzheimers, Bradby said. We    stood in front of that mirror. She said, Who is that lady? I    said, Oh, Aunt Annie Ruth. Thats you!  <\/p>\n<p>    Annie Ruths husband, Charlie, passed away before she did, and    its not uncommon for spouses to precede loved ones with    Alzheimers in death. Caring for someone suffering from the    disease, which progressively robs people of memory, cognition,    muscle movement and personality, can take a heavy toll.    Caregivers experience high levels of stress and cope with    depression, often neglecting their own health and missing    doctors appointments.  <\/p>\n<p>    Those who take care of people with Alzheimers and other forms    of dementia are twice as likely to report substantial    emotional, financial and physical difficulties as other    caregivers, according to the Alzheimers Association. Two    thirds are women, and 34 percent are age 65 or older. A quarter    of caregivers are considered a sandwich generation, meaning    that theyre also taking care of a child under the age of 18.  <\/p>\n<p>    Research has shown that Alzheimers is twice as likely to    affect African Americans (and 1.5 times more likely to affect    Hispanics) than non-Hispanic whites, but until about 10 years    ago there was little research into why the disease strikes    African Americans with such ferocity.  <\/p>\n<p>    The answer is gradually coming into focus, thanks in part to    the research of Dr. Goldie Byrd, the founding director of    COAACH, which opened in 2014. A recent article by journalist    and novelist Marita Golden in the Washington Post    described the Greensboro center as a kind of ground zero for    innovative, cross-disciplinary and community-based responses to    the disease.  <\/p>\n<p>    A complex interplay of environmental and genetic factors    accounts for why Alzheimers inflicts a disparate toll on    African Americans. An understanding of the interplay can help    people make lifestyle choices that reduce the risk of the    diseases onset, and researchers hope that understanding    genetic factors will lead to the development of drugs to treat    it. Alzheimers medications currently only address symptoms,    without preventing, curing or slowing the disease.  <\/p>\n<p>    On the environmental side of the equation, a series of studies    presented at the 2017 Alzheimers Association International    Conference in London in July added to a growing body of    evidence that racial inequities increase the risk of    Alzheimers and other dementias. Researchers at the University    of Wisconsin found that African Americans were 60 percent more    likely than whites to experience a stressful life event such as    losing a job, the death of a child, combat, or growing up with    a parent who abused drugs, which correlated with deterioration    in cognition later in life. Other studies presented at the    conference found that people born in states with high infant    mortality rates a proxy for harsh early-life conditions     and neighborhoods disadvantaged by poverty, poor housing and    limited educational and employment opportunities were more    likely to experience poorer cognitive function and dementia    late in life.  <\/p>\n<p>    Despite the diseases disparate impact, the science of how    Alzheimers affects African Americans was woefully behind as    recently as 15 years ago. Byrd joined the faculty at NC A&T    as chair of the biology department in 2003, and that year she    completed a sabbatical at the Duke Center for Human Genetics,    where she helped initiate a study on Alzheimers. At the time,    the university had 7,000 blood samples, but less than 50 were    drawn from African-American volunteers.  <\/p>\n<p>    We wanted to increase our knowledge about Alzheimers,    particularly underrepresented groups like African Americans and    Hispanics, Byrd said. These groups had a disproportionate    burden, but there was so little in the literature about    Alzheimers in these groups, particularly Alzheimers    relationship to genetics.  <\/p>\n<p>    As Byrd continued her research at her new post at A&T, the    first challenge was to figure out how to overcome reluctance    among African Americans to participating in studies.  <\/p>\n<p>    We began by going into the community and asking different    stakeholders  lay people, the faith-based communities; we went    to health fairs and barbershops  and we asked people if they    would participate in a study, Byrd recalled. What would the    barriers be? What would the motivations be?  <\/p>\n<p>    Distrust among African Americans due to the legacy of    atrocities like the Tuskegee experiment a project    launched by the US Public Health Service in 1932 in which    researchers studied black men with syphilis without their    informed consent and without treating them for the disease    was an obvious hurdle. And while there are continuing    reasons for African Americans and other underrepresented groups    to distrust the medical establishment, Byrd emphasized that    ethical research coupled with culturally calibrated outreach    can overcome barriers.  <\/p>\n<p>    People struggle with lack of access and the indifference when    theyre treated even in 2017, Byrd said. They notice when    they go to the doctor and they dont see people who look like    them in 2017. There are recent studies that show that people of    color dont get the same level of care.  <\/p>\n<p>    African Americans will participate in studies, she added.    Stereotypically, people think African Americans wont    participate because of these atrocities. There are very good    reasons for there to be hesitation and concern. We have to take    the time to communicate with them to make sure they feel    comfortable. We cant assume people who are mistreated are    going to be at the front of the line unless we as researchers    assure them that theyre safe, that were going to handle them    and their specimens in an honest and respectful way, and we    reassure them they can stop at any time.  <\/p>\n<p>    The family-support component that became a core pillar of the    COAACH center emerged as natural extension of Dr. Byrds    understanding that she needed to design a study that would earn    the trust of African-American volunteers.  <\/p>\n<p>    The person I was working with  we agreed we would create an    environment that specifically targeted African Americans and    engaged them directly in what the study was, that would create    learning opportunities for this community, that would keep them    engaged and keep them in the loop around whats happening with    the research, Byrd said.  <\/p>\n<p>    Although COAACH opened in response to a need to engage African    Americans in Alzheimers research, Byrd and other staff members    emphasize that the programs at the center are open to people of    all races.  <\/p>\n<p>    We created our COAACH center to assure not only African    Americans but people of all races that we were there, and we    werent going to get them into the study and leave, Byrd said.    If people needed information about diabetes, which is linked    to Alzheimers, they could call. If a church was having a    health fair, they could call. We created a support group that    people can attend; they dont have to be African American. They    can attend Lunch & Learn.  <\/p>\n<p>    Through Dr. Byrds efforts, the bank of data on African    Americans with Alzheimers has dramatically expanded. As part    of the Alzheimers Disease Genetics Consortium, which includes    several other institutions, Byrd was part of a study that    dramatically expanded the number of DNA specimens under review.    In 2013, the consortium discovered that a variation in the    ABCA7 gene that had previously been linked to Alzheimers was    found to have a stronger link in African Americans than    non-Hispanic whites.  <\/p>\n<p>    Finding a gene link like ABCA7 gives researchers clues about    what causes Alzheimers because variants might cause it to    dysfunction and affect different populations in different ways.  <\/p>\n<p>    In the hope of learning more about how genetics factors into    the disease, COAACH is recruiting families with more than one    member who has Alzheimers for an ongoing study. The center has    collected samples from people in North Carolina, along with    Virginia and New York.  <\/p>\n<p>    There may be other genes like ABCA7 that are associated with    the disease, Byrd said. There may be [treatments] that are    specific to one population and not to another. Thats important    because if we only did research in one population everything    ends up being generalized. Our hope is there will be therapies    and interventions that are specific to populations and not    generalized. The advantage of doing studies is that well be    much more inclusive and everyone will benefit.  <\/p>\n<p>    There are many studies and clinical trials going on right    now, she continued. We dont have any cure right now. We    dont have anything to slow the disease. There are drugs that    can assist with the symptoms. We are very hopeful that the    pharmaceutical companies working with research institutions    will come up a drug that can halt or slow the disease.  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Read more here:<br \/>\n<a target=\"_blank\" href=\"https:\/\/triad-city-beat.com\/forget-me-not\/\" title=\"Forget me not - Triad City Beat\">Forget me not - Triad City Beat<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> The community room looks like the interior of any well-appointed modern house from Starmount to Summerfield, with ocean-blue walls, mahogany-style tables matched with high-backed chairs, a sleek metallic refrigerator and comfortable couches. Theres one key difference: The dining room, kitchen, living area and bathroom are collapsed into one large room with no dividers.  <a href=\"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/human-genetics\/forget-me-not-triad-city-beat\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[27],"tags":[],"class_list":["post-213160","post","type-post","status-publish","format-standard","hentry","category-human-genetics"],"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/213160"}],"collection":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/comments?post=213160"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/213160\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/media?parent=213160"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/categories?post=213160"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/tags?post=213160"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}