Quizzes Flashcards

1
Q

What is the commonality between all the MNS disorders?

a. They all exhibit symptoms and measurable impairments attributable to brain dysfunction.
b. They all are a consequence of uncontrolled inflammation.
c. They all have plaques, or proteinaceous aggregates.
d. They all are transmissible from person-to-person.

A

A

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2
Q
A
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3
Q

Which of the following are clinical therapeutic interventions for MNS disorders? ______
a. Increased presence of behavioral therapists at schools.
b. Use of antipsychotic drugs for schizophrenia or antidepressants for mood disorders.
c. Policies and legislations to reduce access to the means of suicide.
d. Better training of teachers and nurses to recognize and identify MNS disorder symptoms.

A

B

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4
Q

There are various ways to treat MNS disorders. These are? ______
a. Targeting the vectors, or vehicles, of MNS disorders.
b. By enacting legislation that protects children from sources of mental or physical sickness.
c. Through the use of antipsychotics.
d. By a combination of therapeutic, psychological, and social interventions.

A

D

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5
Q

To implement and maintain an effective MNS disorders intervention, lawmakers and funding agencies need _______.
a. To be able to recover the costs incurred.
b. Evidence of a positive effect on health and their costs and cost-effectiveness.
c. To familiarize themselves with the problem by hiring affected individuals to lead the efforts.
d. To familiarize themselves with the problem by infecting communities and see the outcome.

A

B

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6
Q

The mortality of MNS disorders is difficult to measure or estimate because _______.
a. MNS disorders result in stillbirths.
b. MNS disorders increase the risk of premature death without being the actual cause of death.
c. MNS disorders are chronic diseases that do not result in death.
d. MNS disorders are overrepresented in certain populations but absent in others.

A

B

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7
Q

MNS disorders are complex because they can be affected and modulated by _______.
a. Age, genetics, religion, and socioeconomic status of the patient.
b. Month of birth, weight, height, and horoscope.
c. All of the above.
d. (a) and (b) only.

A

A

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8
Q

Which of the following attributes of health systems must be considered when analyzing possible interventions for MNS disorders? ______
a. Universality, despite social status.
b. Inclusiveness of MNS disorders in health care packages or insurance schemes.
c. That insurance will pay nurses who are up-to-date and well informed on social events.
d. The age at which must MNS disorders strike, and ensuring this population is covered.

A

B

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9
Q

Which of the following is the BEST definition for MNS disorders? ______
a. A group of diseases with similar etiology.
b. A heterogenous group of clinical manifestations that are affected, and caused, by a complex array of genetic, biological, psychological, and social factors.
c. A group of disorders with unknown etiology.
d. A political term to group all diseases/disorders not covered by governmental health systems.

A

B

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10
Q

Which of the following statements is True for MNS disorders? ______
a. They are grouped together because they all owe their symptoms to a brain disfunction.
b. They are all treated with the same therapeutic regimen.
c. They are exclusive and never co-occur in the same individual.
d. They often are acute and easy to treat.

A

A

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11
Q

What is the monoamine hypothesis when referring to mental illnesses? ______
a. Is a disbalance of proteins in the brain resulting in neurodegeneration.
b. It refers to the unique situation when all monoamine neurotransmitters are in a balanced state, which results in either mania or depression.
c. Is a depletion in the levels of serotonin, norepinephrine, and/or dopamine (single amine neurotransmitters) relative to each other.
d. All of the above.
e. (a) and (b) only.

A

C

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12
Q

Three vehicles, or means, to deliver interventions against MNS disorders are:

A

population
community
healthcare

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13
Q

Under the healthcare platform, there are various levels at which interventions can take place. These are:

A

Self management
primary care / community outreach
hospital care

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14
Q

Three factors that have contributed to a steady increase in MNS disorders in recent times are:

A

aging - people are living longer
population growth - overcrowding - streching resources
lifestyle factors - long work hours, poor nutrition

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15
Q

MNS disorders manifest broadly and differently because they can be modulated by several factors, including: (mention at least 3)

A

Genetic
Biological
Psychological
Social

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16
Q

T/F MNS disorders are a catchall term for diseases and disorders that are usually treated equally.

A

F
MNS - Mental Neurological Substance abuse

heterogenious group of disorders/disease including the above - are not treated equally

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17
Q

T/F Interventions to reduce or prevent MNS disorders have benefits for society (i.e. less injuries due to alcohol or drug use).

A

T

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18
Q

T/F If we want to make a positive change on how we manage and prevent MNS disorders, political will and commitment from development agencies to allocate the necessary resources and provide technical leadership is essential.

A

T

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19
Q

T/F Crude mortality numbers are used to estimate the medical burden of MNS disorders because they are the direct cause of substantial deaths.

A

F
Use YYLs (years of life lost)
YLDs (years lived with diablility)
DALYs (disablility adjusted life years)

to esitmate medical burden beacuse MNS disorders increase risk of death without it being the direct cause

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20
Q

There are various causes for dementia, many treatable. Which of the following is treatable? _____
a. Certain dementias as a result of stroke
b. Kuru
c. Frontal lobe degeneration
d. Brain tumor that has destroyed brain tissue

A

A

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21
Q

The molecular composition of the Alzheimer’s plaques and fibers are _____.
a. Prion protein and microtubules, respectively.
b. Prion protein and tau protein, respectively
c. Amyloid-β and microtubules, respectively.
d. Amyloid-β and and tau protein, respectively.

A

D

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22
Q

What may explain the relatively common occurrence of dementia in young adults with Down syndrome?
_____
a. Increased levels of Amyloid-β due to extra copy of the APP gene.
b. Increased levels of tau protein due to extra copy of the chromosome 18.
c. Increased expression of apolipoprotein in their brains.
d. Increased expression of α-synuclein due to extra copy of the SNCA gene.

A

A

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23
Q

Which of the following are correct comparisons between prion disease and dementia syndromes? _____
a. Both exhibit increased inflammation.
b. Both exhibit dementia as early-on symptoms.
c. Both exhibit pathologically clear proteinaceous aggregates.
d. Both exhibit uncontrolled influx of immune cells.

A

C

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24
Q

Which of the following describes Parkinson’s disease? _____
a. A motor disorder, that is, an excess or deficiency of movement impulse, movement automaticity, and/or muscle tone.
b. A type of metabolic disorder, where disturbances in the sodium concentration of serum alters the electrolytes/osmolality of the nerve cells.
c. A memory disorder, where the main basis for memory, long-term potentiation and long-term depression, is affected.
d. A muscle disorder, where the muscles waste away and hence there is pronounced overall slowness of motion.

A

A

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25
Q

Inflammation negatively affects Alzheimer’s and Parkinson’s pathology because _____.
a. It removes the protein aggregates but, as collateral damage, kills the neurons.
b. It destroys the infected cells, but then the immune cells become infected.
c. It destroys the muscles, resulting in motor problems and eventual paralysis.
d. It destroys the good microbiota of the brain, enhancing the pathology.

A

A

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26
Q

Why inhibitors of cholinesterase alleviate Alzheimer’s and Parkinson’s early symptoms? _____
a. They disassemble the plaques.
b. They prevent accumulation of the prion-like components of these diseases.
c. They increase the neurotransmitter availability, which is affected in these diseases.
d. They help with long-term memory and long-term depression.

A

C

27
Q

Senile plaques, kuru plaques, Lewy bodies, are all examples of _____.
a. Prion proteins
b. Abnormal cellular debris
c. Dementia
d. Hyperphosporylated microtubules

A

B

28
Q

Which of the following are common hallmarks of neurological diseases (infectious and noninfections)?
_____
a. Damaging inflammation, neuronal death, and glutamate toxicity.
b. Glutamate toxicity, protein aggregation, and mitochondrial dysfunction.
c. Neuronal death, gliosis, and inflammation.
d. Impaired clearance of brain wastes, neuronal death, and lymph involvement.

A

C

29
Q

Which of the following are main symptoms in Parkinson’s disease? _____
a. Tremors, abnormal posture and gait.
b. Abnormal gait and memory loss.
c. Memory loss and reduced muscle strength.
d. Reduced muscle strength and memory loss.

A

A

30
Q

T/F Most of the cases of what was previously called “senile dementia” we know now were cases of Alzheimer’s.

A

T

31
Q

T/F The epidemiology of both Alzheimer and Parkinson’s diseases is similar. _____

A

F

Alx - 2x more likely women
african american woman 5x
PD - 3x caucasions

32
Q

T/F Lewy body disease is just one of many synucleinopathies, like Alzheimer’s. _____

A

F

Alz is not a synucleinopathy, it is an amylodosis and tauopathy

33
Q

T/F All of the neurodegenerative diseases mentioned in class are pathologically defined by intracellular or extracellular protein aggregates. _____

A

T

34
Q

T/F In Parkinson’s disease, tau tangles disrupts the cellular transport machinery while amyloid plaques are involved in dissemination/spread of the disease. _____

A

F

(should say) in Alz

35
Q

The mainstay Parkinson’s treatment that can also be used as diagnostic: _______________

A

Levadopa / DA presursor

36
Q

All dementias can be classified into two broad types, these are:________________and_________________.

A

cortical and subcortical

37
Q

Specific anatomical part of the brain affected in Parkinson’s disease (looks dark to the eye): __________________.

A

AD producing neurons in the substantra nigra

38
Q

Oligomers and plaques of ____________________ drive the inflammation in Alzheimer’s.

A

amyloid

39
Q

What are the two types of GBS? _____
a. Axonal and demyelinating
b. Demyelinating and somatic
c. Somatic and axonal
d. None of the above; there is only one (1) type

A

A

40
Q

Which of the following would be the most accurate definition of molecular mimicry in disease? _____
a. An evolved resemblance between an organism and another living or non-living object.
b. Similarities between the antigens of a microbe and a host.
c. When a pathogen sheds its outer coat to copycat the cells of its host.
d. Is one cause of dementia, as the brain can’t differentiate between what’s real and what’s not.

A

B

41
Q

What can be affected in diseases of motor neurons? _____
a. Sensory neurons
b. Microglia
c. Neuromuscular junctions
d. Basal ganglia

A

C

42
Q

In MS, the pathology is driven by an humoral and cellular response towards ______.
a. Oligodendrocytes
b. Schwan cells
c. Microglia
d. BMECs

A

A

43
Q

In MS, there are _____________ as well as ______________ epidemiological oddities. _____
a. Geographical; dietary
b. Geographical; temperature
c. Temperature; dietary
d. Dietary; age

A

A

44
Q

T/F In developed countries, MS is the most common peripheral nervous system (PNS) disease that arises in young adults and causes permanent disability.

A

F

MS is the most common CNS disease not PNS

45
Q

T/F The pathology in GBS is driven by a cellular response towards motor neuron axons. _____

A

F

driven by humoral effects not cellular rxn.

46
Q

T/F GBS occurs when the autoreactive antibodies bind to the myelin sheath on the central nervous system (CNS) nerves.

A

F

GBS is a PNS, not CNS, syndrome

47
Q

T/F MS can strike at any age, but most cases are in people over 40.

A

F

cases are mostly 20-40 yrs old

48
Q

T/F A temporary remission from GBS symptoms occurs when women are pregnant.

A

F

pregnancy is protective

49
Q
A
50
Q
A

the main reason MS is permanent is because the immune response is generated against self-antigens.

51
Q

Which of the following is NOT a player in the Gut-Brain axis? _____
a. The microbiota
b. The vagus nerve
c. The stomach
d. Bacterial metabolites

A

C

52
Q

Mental illnesses can be classified into the following categories: _____
a. Mood disorders, cognition disorders, and behavioral disorders.
b. Depression, anxiety, and psychosis.
c. Neurodegenerative, primary, and secondary.
d. Anxiety, eating, and behavioral disorders.

A

A

53
Q

Which of the following statements BEST describe the gut-brain axis? _____
a. A direct bidirectional communication between the central and the enteric nervous system.
b. A one-way link between the gut and the brain.
c. A two-way link between the gut and the enteric nervous system.
d. A bidirectional link between the gut and the brain mediated by several signals.

A

D

54
Q

Which of the following is an example of a microbe influencing behavior? ______
a. C. jejuni gastrointestinal infection driving GBS
b. Brain infections by biofilm-forming bacteria promoting Alzheimer’s disease
c. Rabies infection turning the infected aggressive
d. Herpes virus infection increasing the risk for Multiple sclerosis.

A

C

55
Q

How is the “hygiene hypothesis” related to the gut microbiota? ______
a. The human microbiota is necessary to train the immune system, and this period of immune training is disrupted by the extremely clean household environments.
b. The lack of exposure to microbes early in life increases the risk for autoimmune diseases like as asthma.
c. The constant, low grade exposure to antibiotics or hormones (like from dairy or cattle industry) changes the ratio of “bad” and “good” gut microbes, which throws the immune system off, promoting aberrant reactions.
d. All of the above.
e. (a) and (b) only.

A

D

56
Q

T/F Mental illnesses are considered disorders rather than diseases because the causative agent is unknown.

A

T

57
Q

T/F There are three (3) mediators between the gut and the brain: hormones, cytokines, and neuroreactive compounds.

A

T

58
Q

T/F A small change in the gut microbiota can affect the brain, but small changes in the brain does not affect the gut microbiota.

A

F

changes in brain can influence gut (ex. stress)

59
Q

T/F The “monoamine hypothesis” states that a disbalance in the levels of serotonin, norepinephrine (or epinephrine), and dopamine is behind mental illnesses.

A

T

60
Q

T/F The gut-brain axis is an unidirectional communication between the PNS and the gut.

A

F

bidirectional between CNS and GI tract

61
Q

Three (3) types of bacterial metabolites that can affect brain’s function: ____________________,
__________________, and ______________________.

A

Neurotransmiters
Short Chain Fatty Acids
tytophtophan metabolites

62
Q

Three (3) mental diseases/disorders where there is a clear correlation with gut dysbiosis:
____________________, __________________, and ______________________.

A

Depression/Anxiety
Autism
Obesity

63
Q

Four (4) ways by which the gut-brain axis can affect health and disease: ______________________,
______________________, ______________________, and ____________________.

A

inflamation - leaky gut
stress - high cortosisol
high cortosisl - inflamation
gut dysbiolsis - inflamation

64
Q
A