Table of Contents
The brainβs main function in the central nervous system is to make sure that the neuron signals that the brain produces are transferring throughout the entire body. These neuron signals also have a function as they help the body feel pain, sense moods, aid in organ function, and have a bidirectional connection to the brain as the body sends the signals back and forth. When there are unwanted pathogens that start to disrupt the neuron signals and start to affect the brain, it can lead to neurodegenerative disorders causing the entire body to be dysfunctional. In this 2 part series, we will be taking a look into what is Alzheimerβs and how does it affect the brain. In Part 2, we will take a look at what S.H.I.E.L.D. is and how can it help prevent Alzheimerβs disease from progressing further in the brain. By referring patients to qualified and skilled providers who specialized in neurological services. To that end, and when appropriate, we advise our patients to refer to our associated medical providers based on their examination. We find that education is the key to asking valuable questions to our providers. Dr. Alex Jimenez DC provides this information as an educational service only. Disclaimer
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Can my insurance cover it? Yes, in case you are uncertain here is the link to all the insurance providers we cover. If you have any questions, please call Dr. Jimenez at 915-850-0900.
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So Alzheimerβs disease is the most common form of dementia in the elderly that ranges from ages 65 and older. About 5.5 million patients in the U.S. would spend about $300B per year in medical costs while getting treated for Alzheimerβs. Research shows that since Alzheimerβs disease is a progressive neurologic disorder, it will cause brain shrinkage and cause brain cells to die over time. Some of the major risk factors that can cause Alzheimerβs disease to progress in an individual are family history, age, head injury, stroke, high blood pressure, and gender. It turns out that females actually make up about 2/3 of developing Alzheimerβs disease.Β Other research studies have shown that Alzheimerβs disease is classified as preclinical or presymptomatic depending on how severe the cognitive impairment is in a person. Since about 30-40% over the age of 85 have Alzheimerβs disease the current lifespan is about 80 years.
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Since age plays a huge role as a risk factor to aid the progression of Alzheimerβs disease the symptoms can actually range from mild to severe as research found that when there is damage to the brain, Alzheimerβs disease can start in a decade or more before memory loss and other cognitive problems start to appear as it progresses. Even though Alzheimerβs is starting in the preclinical stage, a person may look symptom-free, however, the changes are taking place in the brain and causing cognitive disorders. Some of the symptoms of Alzheimerβs disease actually depends on how severe is the progression and they include:
Stem cells* or HCTP (human cellular tissue products) have been used in both international and nationally affiliated clinics and distribution organizations to help boost the bodyβs own natural healing process. As a form of regenerative cellular treatment, HCTP can help repair and regenerate damaged cells, tissues, and organs back to their original state and function properly in the body. As more and upcoming research finds more information on the beneficial properties of HCTP and its uses, individuals with chronic pain can begin their wellness journey pain-free.
In a normal healthy brain, the brain does shrink naturally while still retaining normal cognitive functions, like memory skills and motor skills. In an Alzheimerβs brain, the brain is shrunk but the cognitive functions are disrupted causing neurodegenerative disorders. Research shows that Alzheimerβs disease causes widespread damage to the brain causing many neurons in the brain to stop functioning, lose connection and eventually die. Not only that but in an Alzheimerβs brain, it will form plaque modules known as amyloid plaque and neurofibrillary tangles in the brain.
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Studies have found that the correlation of the behavioral symptoms of Alzheimerβs disease is due to the accumulation of amyloid plaques and neurofibrillary tangles in the brain causing damage and destruction to memory and cognitive function. Surprisingly, there are actually three tauopathies that can cause neuroinflammation to the brain and cause the start of cognitive decline. All three of these induced tauopathies require decades of tangles and neuroinflammation spreading through the brain eventually leading to dementia, which likely begins early in life, e.g. CTE and playing football as a young adult. These three tauopathies are:
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Other studies have found that the neuropathological alternations in an Alzheimerβs brain can cause lesions to the brain while having an abundance of amyloid plaques and neurofibrillary tangles infesting the brain. This will cause neuronal dysfunction and degeneration to the brain causing cognitive disorders to progress further and causing the individual to have neurological problems as research shows.
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Overall, the brainβs main function in the central nervous system is to transport neuron signals all throughout the body in a bidirectional connection as the neuron signals help keep the body functional and working properly. When neurodegenerative disorders like Alzheimerβs disease start to affect the brain, it can cause amyloid plaques and neurofibrillary tangles to infest the brain and disrupt the neuron signals in the brain. By treating Alzheimerβs disease from progressing further in the brain with whole nutritious food and exercising regularly (both mentally and physically) can help improve brain function as well as improve memory function in older adults.
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Bloom, George S. βAmyloid-Ξ² and Tau: The Trigger and Bullet in Alzheimer Disease Pathogenesis.β JAMA Neurology, U.S. National Library of Medicine, Apr. 2014, pubmed.ncbi.nlm.nih.gov/24493463/.
Kumar, Anil, et al. βAlzheimer Disease.β StatPearls [Internet]., U.S. National Library of Medicine, 11 Aug. 2021, www.ncbi.nlm.nih.gov/books/NBK499922/.
Medical Professionals, NIA. βWhat Are the Signs of Alzheimerβs Disease?β National Institute on Aging, U.S. Department of Health and Human Services, 16 May 2017, www.nia.nih.gov/health/what-are-signs-alzheimers-disease.
Medical Professionals, NIA. βWhat Happens to the Brain in Alzheimerβs Disease?β National Institute on Aging, U.S. Department of Health and Human Services, 16 May 2017, www.nia.nih.gov/health/what-happens-brain-alzheimers-disease.
Paulson, Jennifer B, et al. βAmyloid Plaque and Neurofibrillary Tangle Pathology in a Regulatable Mouse Model of Alzheimerβs Disease.β The American Journal of Pathology, American Society for Investigative Pathology, Sept. 2008, www.ncbi.nlm.nih.gov/pmc/articles/PMC2527075/.
Serrano-Pozo, Alberto, et al. βNeuropathological Alterations in Alzheimer Disease.β Cold Spring Harbor Perspectives in Medicine, Cold Spring Harbor Laboratory Press, Sept. 2011, www.ncbi.nlm.nih.gov/pmc/articles/PMC3234452/.
Staff, Mayo Clinic. βAlzheimerβs Disease.β Mayo Clinic, Mayo Foundation for Medical Education and Research, 19 Feb. 2022, www.mayoclinic.org/diseases-conditions/alzheimers-disease/symptoms-causes/syc-20350447.
Professional Scope of Practice *
The information herein on "How To Detect Alzheimer's In The Brain | Part 1" is not intended to replace a one-on-one relationship with a qualified health care professional or licensed physician and is not medical advice. We encourage you to make healthcare decisions based on your research and partnership with a qualified healthcare professional.
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Our information scope is limited to Chiropractic, musculoskeletal, acupuncture, physical medicines, wellness, contributing etiological viscerosomatic disturbances within clinical presentations, associated somatovisceral reflex clinical dynamics, subluxation complexes, sensitive health issues, and/or functional medicine articles, topics, and discussions.
We provide and present clinical collaboration with specialists from various disciplines. Each specialist is governed by their professional scope of practice and their jurisdiction of licensure. We use functional health & wellness protocols to treat and support care for the injuries or disorders of the musculoskeletal system.
Our videos, posts, topics, subjects, and insights cover clinical matters, issues, and topics that relate to and directly or indirectly support our clinical scope of practice.*
Our office has reasonably attempted to provide supportive citations and has identified the relevant research studies supporting our posts. We provide copies of supporting research studies available to regulatory boards and the public upon request.
We understand that we cover matters that require an additional explanation of how it may assist in a particular care plan or treatment protocol; therefore, to further discuss the subject matter above, please feel free to ask Dr. Alex Jimenez, DC, or contact us at 915-850-0900.
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Dr. Alex Jimenez DC, MSACP, RN*, CCST, IFMCP*, CIFM*, ATN*
email: coach@elpasofunctionalmedicine.com
Licensed as a Doctor of Chiropractic (DC) in Texas & New Mexico*
Texas DC License # TX5807, New Mexico DC License # NM-DC2182
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Compact Status: Multi-State License: Authorized to Practice in 40 States*
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Dr. Alex Jimenez DC, MSACP, RN* CIFM*, IFMCP*, ATN*, CCST
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