Alzheimer's Disease Research Paper

Superior Essays
Down Syndrome and Alzheimer’s Disease
Leah McCarvill
Post University Abstract
Down syndrome and Alzheimer’s disease has been studied to see if there is a biological connection. It has been noted that individual’s with Down syndrome commonly have Alzheimer’s disease later in life. The biological evidence found to connect Down Syndrome and Alzheimer’s disease will be discussed. The correlation between the genetics and biological evidence between the general population and the Down Syndrome population have been the object of many studies which have led to the importance of early detection and treatment for individuals with Down Syndrome.

Down syndrome and Alzheimer’s disease
Down syndrome and Alzheimer’s disease has been studied
…show more content…
The biological evidence found to connect Down Syndrome and Alzheimer’s disease will be discussed.
Down Syndrome
The genes that carry the codes which are responsible for one’s inherited traits are grouped in long rod-like structures called chromosomes. Most cells contain 23 pairs of chromosomes. One inherits half of the pair of 23 chromosomes from each parent. In individuals born with Down syndrome only a full or partial copy of the chromosome 21. The additional genetic material causes alterations in the course of development. These alteration causes specific characteristics that are associated with Down syndrome. There are several common physical traits of Down syndrome can include; “low muscle tone, small stature, an upward slant to the eyes, and a single deep crease across the center of the palm” (Ndss, 2012). As with many inherited traits not every individual will have all of these traits in the same degree or not at all. There are three types of Down syndrome. Trisomy 21 or nondisjunction which is the result of an embryo having three
…show more content…
The evidence of the uncommonly high diagnosis of Alzheimer’s disease in individuals with Down syndrome appears to the main trigger for these studies. This trigger is noted in the study published in Alzheimer's & Dementia: Translational Research & Clinical Interventions “Down syndrome (DS) is associated with an increased rate of Alzheimer's-like dementia, prevalent in up to 55% of individuals in their forties and 77% of age >60 years. Neuritic plaques and neurofibrillary tangles consistent with Alzheimer's disease (AD) have been identified in nearly all DS adults examined of age >40 years.” (Matthews et al., 2016). The connection between Down syndrome and Alzheimer’s disease it seems can be found in the exact cause of Down syndrome. It is hypothesized that due to the third copy of chromosome 21 in all cells particularly the amyloid precursor protein (APP) could be part of the connection to Alzheimer’s disease being so prevalent in individuals with Down syndrome even though scientists are not clear on all of the functions of APP. It is noted in an article on the Alzheimer’s Association website “One of the brain’s APP processing pathways produces beta-amyloid, a fragment that’s the chief component of plaques and a prime suspect in Alzheimer’s related brain changes.” (Alzheimer’s Association, 2016). The third copy of chromosome 21 appears to be the main focus of most

Related Documents

  • Improved Essays

    Trisomy 21 Research Paper

    • 1600 Words
    • 7 Pages

    Describe trisomy 21. Trisomy 21 is a genetic disorder commonly known as Down syndrome. It is caused by the presence of all or part of an extra 21st chromosome. IT is the most common chromosomal abnormality associated with intellectual disability. One in 730 live births results in trisomy 21.…

    • 1600 Words
    • 7 Pages
    Improved Essays
  • Improved Essays

    Charles J. Epstein was a highly regarded geneticist who made tremendous contributions to the medical field during his lifetime. He was born on September 3, 1933 in Philadelphia, Pennsylvania to Jacob C. Epstein and Frieda Epstein, Jewish immigrants from the Ukraine. During his high school years at Central High School, he excelled at academics and enjoyed track and field, and played the cello. After completing high school he went on to Harvard College where he graduated summa cum laude and received a chemistry degree. He married his girlfriend and fellow Harvard student, Lois Barth, despite being warned to wait until after they had both completed medical school.…

    • 954 Words
    • 4 Pages
    Improved Essays
  • Improved Essays

    He first described the condition as “Mongolism,” but was later changed to Down syndrome. Trisomy 21 is an abnormality in chromosome 21. What causes the condition is the added chromosome to human chromosome 21. This chromosome is very important as it contains about 300 genes that create our body. The extra genetic material completely changes the normal development of a human, causing Down syndrome.…

    • 652 Words
    • 3 Pages
    Improved Essays
  • Improved Essays

    As one ages, new and more difficult physical and mental health problems arise. Among those issues are diseases such as arthritis, dementia, and osteoporosis. In particular, Dementia is a syndrome that results in the loss of memory and other intellectual capabilities occurring most often as one ages, “affecting 1.4 million people and their families” (LBD Association). Lewy Body Dementia is the second most common type of dementia following Alzheimer's. The disease causes degeneration of the brain thus resulting in a decline in cognitive thinking, reasoning and muscle movement.…

    • 1682 Words
    • 7 Pages
    Improved Essays
  • Improved Essays

    Dementia Assessment Paper

    • 2376 Words
    • 10 Pages

    Traditional assessment tools for the diagnosis of dementia are usually not suitable when evaluating individuals with intellectual and developmental disabilities (IDD). In addition, the majority of healthcare providers is not armed with the training and experience needed to care for that population holistically. This paper centers on: the progressive changes that occur with dementia especially for individuals with Down Syndrome (DS); the various types of dementia and a focus on Alzheimer’s disease (AD); assessments specifically for the IDD population; and the importance of creating a support system for the individual their advocates; most importantly the need for an interdisciplinary team to have the necessary tools to provide the right care for this population. Intellectual and Developmental Disabilities (IDD) formally referred to as Mental Retardation is a condition,…

    • 2376 Words
    • 10 Pages
    Improved Essays
  • Great Essays

    This occurs when a pair of the twenty first chromosome in the egg or sperm does not properly divide, resulting in the child having three copies of chromosome 21 instead of just two. The extra copy of chromosome 21 is reproduced in every cell of the unborn child’s body. This type of Down Syndrome is more common than any other type. It is the cause behind 95% of all people with Down syndrome (“Facts about Down Syndrome”).…

    • 1829 Words
    • 8 Pages
    Great Essays
  • Improved Essays

    Causes Of Down Syndrome

    • 1530 Words
    • 7 Pages

    Down Syndrome affects physical growth, facial characteristics, and intellect. Also known as Trisomy 21, it is a genetic mutation in which a person is born with an extra chromosome. These chromosomes are rod-like structures where genetic materials are stored and grouped. The nucleus of each cell in the human body contains 23 chromosomes, half, being inherited from each parent. The added chromosome changes the systematic development, affecting not only physical traits but mental as well.…

    • 1530 Words
    • 7 Pages
    Improved Essays
  • Improved Essays

    As I said, chromosome 21 is one of the smallest chromosomes in the human body and represents approximately 1.5% of the DNA in cells. It was also the second human chromosome to be fully sequenced, after chromosome 22. Some of the genes located on chromosome 21 include APP, CBS, and HLCS; which stands for amyloid beta precursor protein, cystathionine-beta-synthase, and holocarboxylase synthetase, respectively. These, and other genes, are typically related to proteins and enzymes. One of these, DSCR1, is typically overexpressed in the brains of children with down syndrome and can lead to neurofibrillary tangles, such as those associated with Alzheimer’s disease.…

    • 771 Words
    • 4 Pages
    Improved Essays
  • Great Essays

    Trisomy 21

    • 1700 Words
    • 7 Pages

    An irregularly shaped mouth and a protruding tongue. Body size and shape is also different among people with Down syndrome. As a child, they often grow slowly and are shorter than average as an adult. They have a short, wide neck possibly with excess fat and skin. Weak muscles throughout their body, short stocky arms and legs, small hands/feet and some also have a wide space between the big toe and second toe.…

    • 1700 Words
    • 7 Pages
    Great Essays
  • Improved Essays

    This research paper will discuss what these diseases are, how rare they are, and what characteristics are common with these diseases. Down Syndrome Down syndrome is a chromosomal condition that can’t be cured. It occurs when a child is born with a partial or full copy of chromosome 21. This extra genetic material changes learning and development courses. Some ways to identify if a child has it are: a single,…

    • 1085 Words
    • 5 Pages
    Improved Essays
  • Decent Essays

    Trisomy is a cell that has three copies of one chromosome instead of having the normal two copies. Trisomy 21 is known as the congenital disorder Down syndrome. This occurs when each cell has three copies of chromosome twenty one rather than having a pair. Commonly, Down syndrome is caused by nondisjunction. Nondisjunction is "an error in which homologous chromosomes or sister chromatids fail to separate normally during meiosis or mitosis" (Huether,McCance pp.42).…

    • 285 Words
    • 2 Pages
    Decent Essays
  • Improved Essays

    Genetics Down Syndrome

    • 1457 Words
    • 6 Pages

    Genetics To Down Syndrome Genetics describes the makeup of our cells, genes, chromosomes, and phenotypes. When there is alter in a gene or a duplication of a chromosome, it can lead to a certain diseases. One of the main diseases known today from a duplication of a chromosome is Down syndrome. John Down first put a name to Down syndrome in 1866, but artifacts from Mexico and Saxon documented some cases of Down syndrome in individuals, and also some were found in paintings of the Renaissance in Europe. (Fisher & Hernandez, 1996)…

    • 1457 Words
    • 6 Pages
    Improved Essays
  • Improved Essays

    Down’s syndrome is a very common genetic disorder in babies in today’s society. A genetic disorder is a condition that is caused by an absent, an inactive gene or by a chromosomal abnormality (Dictionary, 2016). Down’s syndrome is caused by an extra chromosome 21 in the genome in an individual. The extra chromosome causes moderate intellectual disability.…

    • 908 Words
    • 4 Pages
    Improved Essays
  • Improved Essays

    Down Syndrome is a mental disability that occurs due to an error in cell division. Although it has not yet been discovered why the extra chromosome twenty-one is created, doctors have noticed that…

    • 675 Words
    • 3 Pages
    Improved Essays
  • Great Essays

    Though it is known that the older a woman is upon giving birth the higher the risk for having a baby with down syndrome, those over the age of thirty five are noted as being more likely, though there are pre-natal screenings available to detect the possibility of the disability CDC, 2014). Most often the cell error occurs during the formation of the egg or sperm, though it can happen less often after fertilization as the embryo is growing (NIH, 2014). In about four percent of cases this is attributed to the father providing an extra chromosome twenty one, where most often in more than ninety percent of cases it is the mother who provides the extra chromosome twenty-one (NIH, 2014). There are three types of chromosome changes which lead to down syndrome: Complete trisomy twenty one, this is where all the persons cells have a complete extra copy; Mosaic trisomy twenty-one, this is where only some cells have the different chromosome; and Translocation trisomy, where only a part of the extra copy of the cell is found in the persons cells (NIH,…

    • 1513 Words
    • 7 Pages
    Great Essays