Information about Aids Dementia Complex
| ICD-10 | B22., F02.4 |
|---|---|
| ICD-9 | 042 |
AIDS dementia complex (ADC; also known as HIV dementia, HIV encephalopathy and HIV-associated dementia) has become a common neurological disorder associated with HIV infection and AIDS. It is a metabolic encephalopathy induced by HIV infection and fueled by immune activation of brain macrophages and microglia.[1] These cells are actively infected with HIV and secrete neurotoxins of both host and viral origin. The essential features of ADC are disabling cognitive impairment accompanied by motor dysfunction, speech problems and behavioral change. Cognitive impairment is characterised by mental slowness, trouble with memory and poor concentration. Motor symptoms include a loss of fine motor control leading to clumsiness, poor balance and tremors. Behavioral changes may include apathy, lethargy and diminished emotional responses and spontaneity. Histopathologically, it is identified by the infiltration of monocytes and macrophages into the central nervous system (CNS), gliosis, pallor of myelin sheaths, abnormalities of dendritic processes and neuronal apoptosis.[2][1]
ADC typically occurs after years of HIV infection and is associated with low CD4+ T cell levels and high plasma viral loads. It is sometimes seen as the first sign of the onset of AIDS. Prevalence is between 10-20% in Western countries[4] and has only been seen in 1-2% of India based infections.[5][6] This has to due to with differences in diets, such as consumption of curcumin (in curry) and EGCG or Theaflavins (in teas), both which can pass the blood brain barrier and have neuroprotective effects. With the advent of highly active antiretroviral therapy (HAART), the frequency of ADC has declined in developed countries. HAART may not only prevent or delay the onset of ADC in people with HIV infection, it can also improve mental function in people who already have ADC.
Dementia only exists when neurocognitive impairment in the patient is severe enough to interfere markedly with day-to-day function. That is, the patient is typically unable to work and may not be able to take care of him or herself. Before this, the patient is said to have a mild neurocognitive disorder.
Diagnostic criteria
- Marked acquired impairment of at least two ability domains of cognitive function (e.g. memory, attention): typically, the impairment is in multiple domains, especially in learning, information processing and concentration/attention. The cognitive impairment is ascertained by medical history, mental status examination or neuropsychological testing.
- Cognitive impairments identified in 1. interfere markedly with day-to-day functioning.
- Cognitive impairments identified in 1. are present for at least one month.
- Cognitive impairments identified in 1. do not meet the criteria for delirium, or if delirium is present, dementia was diagnosed when delirium was not present.
- No evidence of another, pre-existing aetiology that could explain the dementia (e.g. another CNS infection, CNS neoplasm, cerebrovascular disease, pre-existing neurological disease, severe substance abuse compatible with CNS disorder.[7]
While the progression of dysfunction is variable, it is regarded as a serious complication and, untreated, can progress to a fatal outcome. Diagnosis is made by neurologists who carefully rule out alternative diagnoses. This routinely requires a careful neurological examination, brain scans (MRI or CT scan) and a lumbar puncture to evaluate the cerebrospinal fluid. No single test is available to confirm the diagnosis, but the constellation of history, laboratory findings, and examination can reliably establish the diagnosis when performed by experienced clinicians. The amount of virus in the brain does not correlate well with the degree of dementia, suggesting that secondary mechanisms are also important in the manifestation of ADC.
Research
AIDS Dementia Complex (ADC) is not a true opportunistic infection. It is one of the few conditions caused directly by HIV itself. But it is not quite as simple as that because the central nervous system can be damaged by a number of other causes:- opportunistic infections - there are many
- Primary cerebral lymphoma or metastasis of other AIDS-related cancers
- direct effects of HIV in the brain
- toxic effects of drug treatments
- malnutrition
ADC stage characteristics
- Stage 0 (Normal) Normal Mental and Motor Function
- Stage 0.5 (Subclinical) Minimal symptoms of cognitive or motor dysfunction characteristic of ADC, or mild signs (snout response, slowed extremity movements), but without impairment of work or capacity to perform activities of daily living (ADL). Gait and strength are normal.
- Stage 1 (Mild) Evidence of functional intellectual or motor impairment characteristic of ADC, but able to perform all but the more demanding aspects of work or ADL. Can walk without assistance.
- Stage 2 (Moderate) Cannot work or maintain the more demanding aspects of daily life, but able to perform basic activities of self care. Ambulatory, but may require a single prop.
- Stage 3 (Severe) Major intellectual incapacity - cannot follow news or personal events, cannot sustain complex conversation, considerable slowing of all output. And/or motor disability - cannot walk unassisted, requiring walker or personal support, usually with slowing and clumsiness of arms as well.
- Stage 4 (End Stage) Nearly vegetative. Intellectual and social comprehension and responses are at a rudimentary level. Nearly or absolutely mute. Paraparetic or paraplegic with double incontinence
References and notes
1. ^ Gray, F., Adle-Biassette, H., Chrétien, F., Lorin de la Grandmaison, G., Force, G., Keohane, C. (2001). "Neuropathology and neurodegeneration in human immunodeficiency virus infection. Pathogenesis of HIV-induced lesions of the brain, correlations with HIV-associated disorders and modifications according to treatments". Clin. Neuropathol. 20 (4): 146-155. PubMed .
2. ^ Adle-Biassette, H., Lévy, Y., Colombel, M., Poron, F., Natchev, S., Keohane, C. and Gray, F. (1995). "Neuronal apoptosis in HIV infection in adults". Neuropathol. Appl. Neurobiol. 21 (3): 218-227. PubMed .
3. ^ Gray, F., Adle-Biassette, H., Chrétien, F., Lorin de la Grandmaison, G., Force, G., Keohane, C. (2001). "Neuropathology and neurodegeneration in human immunodeficiency virus infection. Pathogenesis of HIV-induced lesions of the brain, correlations with HIV-associated disorders and modifications according to treatments". Clin. Neuropathol. 20 (4): 146-155. PubMed .
4. ^ Grant, I., Sacktor, H., and McArthur, J. (2005). "HIV neurocognitive disorders", in H. E. Gendelman, I. Grant, I. Everall, S. A. Lipton, and S. Swindells. (ed.): The Neurology of AIDS, 2nd, London, UK: Oxford University Press, 357-373. ISBN 0-19-852610-5 .
5. ^ Satishchandra, P., Nalini, A., Gourie-Devi, M., Khanna, N., Santosh, V., Ravi, V., Desai, A., Chandramuki, A., Jayakumar, P. N., and Shankar, S. K. (2000). "Profile of neurologic disorders associated with HIV/AIDS from Bangalore, south India (1989-96)". Indian J. Med. Res. 11: 14-23. PubMed .
6. ^ Wadia, R. S., Pujari, S. N., Kothari, S., Udhar, M., Kulkarni, S., Bhagat, S., and Nanivadekar, A. (2001). "Neurological manifestations of HIV disease". J. Assoc. Physicians India 49: 343-348. PubMed .
7. ^ Grant, I., Atkinson, J. (1995). "Psychiatric aspects of acquired immune deficiency syndrome.", in Kaplan, H.I. and Sadock, B.J. (ed.): Comprehensive textbook of psychiatry, VI, Baltimore, MD: Williams and Wilkins, (Vol.2, Sect. 29.2) 1644-1669. ISBN 0-683-04532-6.
8. ^ Okamoto, Shu-ichi; Y.Kang, C. W.Brechtel, E.Siviglia, R.Russo, A.Clemente, A.Harrop, S.McKercher, M.Kaul, and S.A.Lipton (16 August 2007). "HIV/gp120 decreases adult neural progenitor cell proliferation via checkpoint kinase-mediated cell-cycle withdrawal and G1 arrest". Cell Stem Cell 1: 230-236. Retrieved on 2007-09-24.2007&rft.volume=1&rft.aulast=Okamoto&rft.aufirst=Shu-ichi&rft.pages=230-236&rft_id=http%3A%2F%2Fwww.cellstemcell.com%2Fcontent%2Farticle%2Ffulltext%3Fuid%3DPIIS1934590907000768">
2. ^ Adle-Biassette, H., Lévy, Y., Colombel, M., Poron, F., Natchev, S., Keohane, C. and Gray, F. (1995). "Neuronal apoptosis in HIV infection in adults". Neuropathol. Appl. Neurobiol. 21 (3): 218-227. PubMed .
3. ^ Gray, F., Adle-Biassette, H., Chrétien, F., Lorin de la Grandmaison, G., Force, G., Keohane, C. (2001). "Neuropathology and neurodegeneration in human immunodeficiency virus infection. Pathogenesis of HIV-induced lesions of the brain, correlations with HIV-associated disorders and modifications according to treatments". Clin. Neuropathol. 20 (4): 146-155. PubMed .
4. ^ Grant, I., Sacktor, H., and McArthur, J. (2005). "HIV neurocognitive disorders", in H. E. Gendelman, I. Grant, I. Everall, S. A. Lipton, and S. Swindells. (ed.): The Neurology of AIDS, 2nd, London, UK: Oxford University Press, 357-373. ISBN 0-19-852610-5 .
5. ^ Satishchandra, P., Nalini, A., Gourie-Devi, M., Khanna, N., Santosh, V., Ravi, V., Desai, A., Chandramuki, A., Jayakumar, P. N., and Shankar, S. K. (2000). "Profile of neurologic disorders associated with HIV/AIDS from Bangalore, south India (1989-96)". Indian J. Med. Res. 11: 14-23. PubMed .
6. ^ Wadia, R. S., Pujari, S. N., Kothari, S., Udhar, M., Kulkarni, S., Bhagat, S., and Nanivadekar, A. (2001). "Neurological manifestations of HIV disease". J. Assoc. Physicians India 49: 343-348. PubMed .
7. ^ Grant, I., Atkinson, J. (1995). "Psychiatric aspects of acquired immune deficiency syndrome.", in Kaplan, H.I. and Sadock, B.J. (ed.): Comprehensive textbook of psychiatry, VI, Baltimore, MD: Williams and Wilkins, (Vol.2, Sect. 29.2) 1644-1669. ISBN 0-683-04532-6.
8. ^ Okamoto, Shu-ichi; Y.Kang, C. W.Brechtel, E.Siviglia, R.Russo, A.Clemente, A.Harrop, S.McKercher, M.Kaul, and S.A.Lipton (16 August 2007). "HIV/gp120 decreases adult neural progenitor cell proliferation via checkpoint kinase-mediated cell-cycle withdrawal and G1 arrest". Cell Stem Cell 1: 230-236. Retrieved on 2007-09-24.2007&rft.volume=1&rft.aulast=Okamoto&rft.aufirst=Shu-ichi&rft.pages=230-236&rft_id=http%3A%2F%2Fwww.cellstemcell.com%2Fcontent%2Farticle%2Ffulltext%3Fuid%3DPIIS1934590907000768">
External links
- Price, R.W. (1998). AIDS Dementia Complex. University of California San Francisco. Retrieved on 2006-04-06.
For other uses of "ICD", see ICD (disambiguation).
The International Statistical Classification of Diseases and Related Health Problems (most commonly known by the abbreviation ICD
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Chapter Blocks Title
I Certain infectious and parasitic diseases
II Neoplasms
III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
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Chapter Blocks Title
I Certain infectious and parasitic diseases
II Neoplasms
III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
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The International Statistical Classification of Diseases and Related Health Problems (most commonly known by the abbreviation ICD
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See also
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- Human immunodeficiency virus 1
- Human immunodeficiency virus 2
Classification & external resources
ICD-10 B20-B24
ICD-9 042 - 044
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An infection is the detrimental colonization of a host organism by a foreign species. In an infection, the infecting organism seeks to utilize the host's resources to multiply (usually at the expense of the host).
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Acquired immunodeficiency syndrome (AIDS)
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The Red ribbon is a symbol for solidarity with HIV-positive people and those living with AIDS.
ICD-10 B 24.
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Classification & external resources
The Red ribbon is a symbol for solidarity with HIV-positive people and those living with AIDS.
ICD-10 B 24.
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Encephalopathy literally means disease of the brain. In medical jargon it can refer to a wide variety of disorders with very different etiologies, prognoses and implications.
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- Human immunodeficiency virus 1
- Human immunodeficiency virus 2
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ICD-10 B20-B24
ICD-9 042 - 044
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In animals, the brain or encephalon (Greek for "in the skull"), is the control center of the central nervous system, responsible for behavior. The brain is located in the head, protected by the skull and close to the primary sensory apparatus of vision, hearing,
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Macrophages (Greek: "big eaters", from makros "large" + phagein "eat") are cells within the tissues that originate from specific white blood cells called monocytes.
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Microglia are a type of glial cell that act as the immune cells of the Central nervous system (CNS). Microglia, the smallest of the glial cells, can act as phagocytes, cleaning up CNS debris. Most serve as representatives of the immune system in the brain and spinal cord.
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A neurotoxin is a toxin that acts specifically on nerve cells – neurons – usually by interacting with membrane proteins such as ion channels. Many of the venoms and other toxins that organisms use in defense against vertebrates are neurotoxins.
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In psychology, memory is an organism's ability to store, retain, and subsequently retrieve information. Traditional studies of memory began in the realms of philosophy, including techniques of artificially enhancing the memory.
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Fatigue
Classifications and external resources
ICD-10 R 53.
ICD-9 780.7
DiseasesDB 30079
MedlinePlus 003088
MeSH D005221 The word fatigue
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Classifications and external resources
ICD-10 R 53.
ICD-9 780.7
DiseasesDB 30079
MedlinePlus 003088
MeSH D005221 The word fatigue
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Histopathology (from the Greek histos (tissue) and pathos (suffering)) refers to the microscopic examination of tissue in order to study the manifestations of disease.
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A monocyte is a leukocyte, part of the human body's immune system that protects against blood-borne pathogens and moves quickly (aprox. 8-12 hours) to sites of infection in the tissues. Monocytes are usually identified in stained smears by their large bilobate nucleus.
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Macrophages (Greek: "big eaters", from makros "large" + phagein "eat") are cells within the tissues that originate from specific white blood cells called monocytes.
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The central nervous system (CNS) represents the largest part of the nervous system, including the brain and the spinal cord. Together with the peripheral nervous system, it has a fundamental role in the control of behavior.
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Gliosis is a proliferation of astrocytes in damaged areas of the central nervous system (CNS). Astrocytes are relatively large glial cells and have various functions, including accumulating in areas where neurons have been damaged.
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Myelin is an electrically insulating phospholipid layer that surrounds the axons of many neurons. It is an outgrowth of glial cells: Schwann cells supply the myelin for peripheral neurons while oligodendrocytes supply it to those of the central nervous system.
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Dendritic cells (DCs) are immune cells and form part of the mammalian immune system. Their main function is to process antigen material and present it on the surface to other cells of the immune system, thus functioning as antigen-presenting cells.
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Apoptosis (pronounced ă-pŏp-tŏ’sĭs, apo tō' sis) is a form of programmed cell death in multicellular organisms. It is one of the main types of programmed cell death (PCD), and involves an orchestrated series of biochemical events leading to a
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Curcumin is the principal curcuminoid of the Indian curry spice turmeric, the other two curcuminoids being demethoxycurcumin and Bis-demethoxycurcumin.The curcuminoids are polyphenols and are responsible for the yellow color of turmeric.
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Epigallocatechin gallate (EGCG) is a type of catechin and is the most abundant catechin in tea.
According to one researcher[1] epigallocatechin-3-gallate is an antioxidant that helps protect the skin from UV radiation-induced damage and tumor formation.
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According to one researcher[1] epigallocatechin-3-gallate is an antioxidant that helps protect the skin from UV radiation-induced damage and tumor formation.
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Antiretroviral drugs are medications for the treatment of infection by retroviruses, primarily HIV. Different classes of antiretroviral drugs act at different stages of the HIV life cycle.
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