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Huntington’s Disease. Kate Leary. Causes. Only caused by: Inherited genetic defect Mutation Defect or mutation is a CAG repeat in the HD gene of chromosome 4 CAG repeat abnormal Huntingtin protein synthesized Abnormal Huntingtin protein leads to premature death of nerve cells.
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Huntington’s Disease Kate Leary
Causes • Only caused by: • Inherited genetic defect • Mutation • Defect or mutation is a CAG repeat in the HD gene of chromosome 4 • CAG repeat abnormal Huntingtin protein synthesized • Abnormal Huntingtin protein leads to premature death of nerve cells
Symptoms • Nervous System • Emotional • Physical • Immune System • Digestive System • Accidents • Death
Nervous System – Emotional • Stubbornness and frustration • Mood swings/changes • Unorganized • Difficulty concentrating • Loss of motivation • Loss of ability to interact • Perceived laziness puts stress on relationships • Depression
Nervous System - Physical • Premature death of nerve cells • Loss of short-term memory • Clumsiness • Stumbling • Difficulty walking • Uncontrollable muscle movements • Difficulty with speech • Difficulty swallowing • Less able to sit/stand stably
Immune System • Uncontrollable muscle movements lead to difficulty swallowing • Weight loss and lack of nutrients as a result • Weakened immune system • PRONE TO INFECTION
Digestive System • Difficulty swallowing from uncontrollable muscle movements • Weight loss • Lack of nutrients • Choking
Accidents • Uncontrollable muscle movements lead to: • Falling • Self-injury • Unable to take care of oneself
Death • Depression may lead to suicide • Death can also be cause by: • Falling • Infection • Self-injury • Choking ** Falling and infection are the most common causes of death in Huntington’s Disease.
Treatment Huntington’s disease is incurable, but you can treat some symptoms. • Medication • Movement • Mental • Therapy • Speech • Physical • Psycho
Medication • Movement disorders • Tetrabenazine • Help suppress involuntary movement • Antipsychotic drugs (Haldol &Clozaril) • Side effect of suppressing movements • Psychiatric disorders • Antidepressants (Lexapro, Prozac, Sarafem, & Zoloft) • Antipsychotic drugs • Suppress violent outbursts • Mood-stabilizing drugs • Prevent highs and lows associated with bipolar disorder
Therapy • Psychotherapy • Talk therapy to help with behavioral issues and learn coping mechanisms • Physical therapy • Help strength, flexibility, balance and coordination to reduce falls • Speech therapy • Strengthen muscles associated with speech, swallowing, and eating
Nutrition • Difficulty swallowing = weight loss • Lots of food and often • 3 large meals OR • Many snacks throughout the day • Eat a healthy, well-balanced diet BUT calorie rich • Soften/blend everything to make swallowing less difficult • Do not drink large amounts of liquids during meals to prevent a fake “full feeling” • Take time eating and sit comfortably
Physiology • # of CAG repeats on chromosome 4 • 11-34 = Normal • 37-121 = Huntington’s Disease • Too many repeats lead to production of abnormal Huntingtin protein • Function of Huntingtin protein not known yet • But function does affect basal ganglia • Basal ganglia • Control over movement of body
Physiology Continued • GABA neurons in basal ganglia • Produce GABA neurotrans- mitters (inhibitors) • Stop some “messages” from travelling through basal ganglia • Huntington’s Disease GABA function • Putamen's inhibitory GABA neurons are destroyed • Lead to disinhibition of thalamus and brainstem • Disinhibition = random, frequent motion
Physiology Continued • Putamen • Part of basal ganglia • Helps control movement of body • Projection to SNpc(substantianigrapars compacta) is necessary for movement
Physiology Continued • Huntington’s Disease Putamen • Projection to SNpc destroyed due to abnormal Huntingtin protein • Increased firing of dopamine neurons • Leads to disinhibition of thalamus and brainstem
Bibliography Board, A.D.A.M. Editorial. "Causes, Incidence, and Risk Factors." Huntington's Disease. U.S. National Library of Medicine, 18 Nov. 0000. Web. 06 June 2012. <http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0001775/>. "Cause of Huntington's Disease." EMedTV. Clinaero. Web. 6 June 2012. <http://nervous-system.emedtv.com/huntington's-disease/cause-of-huntington's-disease.html>. "Effects of Huntington's Disease." What Are the Effects of Huntingtons Disease? Neurological Physiotherapy & Rehabilitation Physiotherapists. Manchester NeuroPhysio. Web. 06 June 2012. <http://www.manchesterneurophysio.co.uk/huntingtons/effects.html>. "Genetics and Physiology of Huntington's Disease." Macalester College. Macalester College. Web. 6 June 2012. <http://www.macalester.edu/psychology/whathap/UBNRP/Huntington/neuro.html>. "Huntington's Disease and Diet." Huntington's Disease and Diet. N.p., n.d. Web. 11 June 2012. <http://huntingtondisease.tripod.com/swallowing/id43.html>. "Huntington Disease." Huntington Disease. WebMD. Web. 06 June 2012. <http://emedicine.medscape.com/article/1150165-overview>. "Huntington's Disease (HD) - Pathophysiology." Huntington's Disease (HD) - Pathophysiology. Web. 06 June 2012. <http://www.mdvu.org/library/disease/hd/hd_path.asp>. Nordqvist, Christian. "What Is Huntington's Disease? What Causes Huntington's Disease?" Medical News Today. MediLexicon International, 02 Aug. 2009. Web. 06 June 2012. <http://www.medicalnewstoday.com/articles/159552.php>. Staff, Mayo Clinic. "Definition." Mayo Clinic. Mayo Foundation for Medical Education and Research, 05 May 2011. Web. 06 June 2012. <http://www.mayoclinic.com/health/huntingtons-disease/ds00401/dsection=treatments-and-drugs>. "Huntington Disease." Huntington Disease. WebMD. Web. 06 June 2012. <http://emedicine.medscape.com/article/1150165-overview>.
Questions • In which chromosome does the Huntington’s Disease causing CAG repeat occur? • What are the most common causes of death in Huntington’s Disease? • What are three types of therapy effective in treating Huntington’s Disease?