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词条 Signs and symptoms of Parkinson's disease
释义

  1. Motor symptoms

     Cardinal symptoms  Other motor symptoms 

  2. Neuropsychiatric

  3. Sleep

  4. Perception

  5. Autonomic

  6. Gastrointestinal

  7. Neuro-ophthalmological

  8. References

Signs and symptoms of Parkinson's disease are varied. Parkinson's disease affects movement, producing motor symptoms.[1] Non-motor symptoms, which include dysautonomia, cognitive and neurobehavioral problems, and sensory and sleep difficulties, are also common.[1] When other diseases mimic Parkinson's disease, they are categorized as parkinsonism.

Motor symptoms

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Four motor symptoms are considered cardinal in PD: slowness of movement (bradykinesia), tremor, rigidity, and postural instability.[1] Typical for PD is an initial asymmetric distribution of these symptoms, where in the course of the disease, a gradual progression to bilateral symptoms develops, although some asymmetry usually persists. Other motor symptoms include gait and posture disturbances such as decreased arm swing, a forward-flexed posture, and the use of small steps when walking; speech and swallowing disturbances; and other symptoms such as a mask-like facial expression or small handwriting are examples of the range of common motor problems that can appear.[1]

Cardinal symptoms

Four symptoms are considered cardinal in PD: bradykinesia, tremor, rigidity, and postural instability also referred to as parkinsonism.[1]

  • Tremor is the most apparent and well-known symptom.[1] It is also the most common; though around 30% of individuals with PD do not have tremor at disease onset, most develop it as the disease progresses.[1] It is usually a rest tremor, maximal when the limb is at rest and disappearing with voluntary movement and sleep.[1] It affects to a greater extent the most distal part of the limb, and at onset typically appears in only a single arm or leg, becoming bilateral later during the course of the disease.[1] Frequency of PD tremor is between 4 and 6 hertz (cycles per second). It is a pronation-supination tremor that is described as "pill-rolling", that is the index finger of the hand tends to get into contact with the thumb, and they perform a circular movement together.[1][11] Such term was given due to the similarity of the movement in PD patients with the former pharmaceutical technique of manually making pills.[2] PD tremor is not improved with alcohol intake, as opposed to essential tremor.[1]
  • Rigidity is a characterized by an increased muscle tone (an excessive and continuous contraction of the muscles) which produces stiffness and resistance to movement in joints.[1] Rigidity may be associated with joint pain, with such pain being a frequent initial manifestation of the disease.[1] When limbs of the person with PD are passively moved by others, a "cogwheel rigidity" is commonly seen.[1] Cogwheel-like or ratchety jerks are characterized by the articulation moving as opposed to the normal fluid movement; when a muscle is externally tried to move, it resists at first, but with enough force, it is partially moved until it resists again, and only with further force, will it be moved.[1][18][3] The combination of tremor and increased tone is considered to be at the origin of cogwheel rigidity.[4]
  • Bradykinesia and akinesia: the former is slowness of movement, while the latter is the absence of it.[1] It is the most characteristic clinical feature of PD, and is associated with difficulties along the whole course of the movement process, from planning to initiation and finally execution of a movement.[1] The performance of sequential and simultaneous movements is also hindered.[1] Bradykinesia is the most disabling symptom in the early stages of the disease.[5] Initial manifestations of bradykinesia are problems when performing daily life tasks requiring fine motor control such as writing, sewing, or getting dressed.[1] Clinical evaluation is based in similar tasks consisting such as alternating movements between both hands or feet.[5] Bradykinesia is not equal for all movements or times. It is modified by the activity or emotional state of the subject to the point of some patients who are barely able to walk being capable of riding a bicycle.[1] Generally, patients have less difficulties when some sort of external cue is provided.[1][6]
... immobile patients who become excited may be able to make quick movements such as catching a ball (or may be able to suddenly run if someone screams "fire"). This phenomenon (kinesia paradoxica) suggests that patients with PD have intact motor programmes, but have difficulties accessing them without an external trigger, such as a loud noise, marching music, or a visual cue requiring them to step over an obstacle.[1]
  • Postural instability: In the late stages, postural instability is typical, which leads to impaired balance and frequent falls, and secondarily to bone fractures.[1] Instability is often absent in the initial stages, especially in younger people.[5] Up to 40% of the patients may experience falls and around 10% may have falls weekly, with the number of falls being related to the severity of PD. It is produced by a failure of postural reflexes, along other disease-related factors such as orthostatic hypotension or cognitive and sensory changes.[1]

Other motor symptoms

Other motor symptoms include:

  • Gait and posture disturbances:
    • Shuffling gait[1] is characterized by short steps, with feet barely leaving the ground. Small obstacles tend to cause the patient to trip.
    • Decreased arm-swing[1]
    • Turning 'en bloc, rather than the usual twisting of the neck and trunk and pivoting on the toes, is when PD patients keep their necks and trunks rigid, requiring multiple small steps to accomplish a turn.
    • Camptocormia[1] is a stooped, forward-flexed posture. In severe forms, the head and upper shoulders may be bent at a right angle relative to the trunk.[7]
    • Festination[1] is a combination of stooped posture, imbalance, and short steps. It leads to a gait that gets progressively faster and faster, often ending in a fall.
    • Gait freezing, also called motor blocks, is a manifestation of akinesia.[1] Gait freezing is characterized by a sudden inability to move the lower extremities which usually lasts less than 10 seconds.[1] It may worsen in tight, cluttered spaces, when attempting to initiate gait or turning around, or when approaching a destination.[1] Freezing improves with treatment and also with behavioral techniques such as marching to command or following a given rhythm.[1]
    • Dystonia[1] is abnormal, sustained, sometimes painful twisting muscle contractions, often affecting the foot and ankle (mainly toe flexion and foot inversion), which often interferes with gait.
    • Scoliosis is abnormal curvature of the spine.[1]
  • Speech and swallowing disturbances:
    • Hypophonia[1] (soft speech)
    • Monotonic speech - quality tends to be soft, hoarse, and monotonous[1]
    • Festinating speech - excessively rapid, soft, poorly intelligible speech
    • Drooling is most likely caused by a weak, infrequent swallow.[1]
    • Dysphagia is an impaired ability to swallow, which in the case of PD is probably related to an inability to initiate the swallowing reflex or by a too long laryngeal or oesophageal movement.[1] It can lead to aspiration pneumonia.
    • Dysarthria is a form of speech disorder.[1]
  • Other motor symptoms and signs:
    • Fatigue
    • Hypomimia[1] (a mask-like face)
    • Difficulty rolling in bed or rising from a seated position[1]
    • Micrographia[1] (small, cramped handwriting)
    • Impaired fine-motor dexterity and motor coordination[1]
    • Impaired gross-motor coordination
    • Akathisia (an unpleasant desire to move, often related to medication)
    • Reemergence of primitive reflexes[1]
    • Glabellar reflex

Neuropsychiatric

Example of reported prevalences of mood problems in PD patients with dementia[1][8]
Mood problem Prevalence
Depression 58%
Apathy 54%
Anxiety 49%

Parkinson's disease causes neuropsychiatric disturbances, which mainly include cognition, mood, and behavior problems, and can be as disabling as motor symptoms.[1]

In most cases, motor symptoms predominate at early PD stages, while cognitive disturbances (such as dementia) emerge later.[9] The onset of parkinsonism in PD relative to dementia is used as an arbitrary criterion to clinically distinguish Parkinson's disease dementia (PDD) and dementia with Lewy bodies (DLB) using a ‘one-year rule’.[9] Dementia onset within 12-months of or at the same time as motor dysfunctions qualified as DLB, whereas in PDD, parkinsonism had to precede dementia by at least one year.[9]

Cognitive disturbances occur even in the initial stages of the disease in some cases.[61] A very high proportion of sufferers have mild cognitive impairment as the disease advances.[1] Most common deficits in nondemented patients are:

  • Executive dysfunction, which translates into impaired set shifting, poor problem solving, and fluctuations in attention among other difficulties[61]
  • Slowed cognitive speed (bradyphrenia)[61]
  • Memory problems can occur, specifically in recalling learned information, with an important improvement with cues. Recognition is less impaired than free recall, pointing towards a retrieving more than to an encoding problem.[61]
  • Regarding language, patients are found to have problems in verbal fluency tests.[10]
  • Visuospatial skills difficulties, which are seen when the person with PD is for example asked to perform tests of facial recognition and perception of line orientation.[10]

Deficits tend to aggravate with time, developing in many cases into dementia. A person with PD has a six-fold increased risk of suffering it,[1] and the overall rate in people with the disease is around 30%.[10] Moreover, prevalence of dementia increases in relation to disease duration, going up to 80%.[10] Dementia has been associated with a reduced quality of life in disease sufferers and caregivers, increased mortality, and a higher probability of moving to a nursing home.[10]

Cognitive problems and dementia are usually accompanied by behavior and mood alterations, although these kinds of changes are also more common in those patients without cognitive impairment than in the general population. Most frequent mood difficulties include:[1]

  • Depression[1] Depression is well recognized in PD, having been identified as "melancholia" by James Parkinson in his original report of the disease in 1817. Estimated prevalence rates of depression vary widely according to the population sampled and methodology used, although depressive symptoms, irrespective of classically defined DSM criteria for depression, are present in 35% of patients[11] There is an increased risk for any individual with depression to go on to develop Parkinson's disease at a later date.[12][13][14] It is increasingly thought to be a consequence of the disease rather than an emotional reaction to disability, although ample evidence shows that the relationship between depression and PD is bidirectional.[15][16] General risk factors for depression are actually stronger markers for depression in PD patients than PD specific factors.[17] Since Parkinson's affects many areas of the brain that control mood (specifically the frontal lobe as well as those areas that produce serotonin, norepinephrine and dopamine), depression may result.[18] Depression is one of the most common neuropsychiatric conditions found in patients who have PD, and it is associated with more rapid progression of physical symptoms and a greater decline in cognitive skills. Depression in patients with PD was found to be more predictive of overall disability than was the motor disability from the PD. An interesting finding is that although a high rate of depression is seen in patients with PD, the incidence of suicide is lower in this group of patients.[19] Many of the symptoms of PD may overlap with those of depression, making diagnosis a difficult issue.[20]
  • Apathy[1]
  • Anxiety[1] is seen; 70% of individuals with PD diagnosed with pre-existing depression go on to develop anxiety. About 90% of PD patients with pre-existing anxiety subsequently develop depression, apathy, or abulia.
Obsessive–compulsive behaviors such as craving, binge eating, hypersexuality, pathological gambling, punding, or others, can also appear in PD, and have been related to a dopamine dysregulation syndrome associated with the medications for the disease.[1]Psychotic symptoms are common in PD, generally associated with dopamine therapy. Symptoms of psychosis, or impaired reality testing, are either hallucinations, typically visual, less commonly auditory, and rarely in other domains including tactile, gustatory, or olfactory, or delusions, that is, irrational beliefs. Hallucinations are generally stereotyped and without emotional content. Initially, patients usually have insight so that the hallucinations are benign in terms of their immediate impact, but have poor prognostic implications, with increased risk of dementia, worsened psychotic symptoms, and mortality. Delusions occur in about 5-10% of treated patients, and are considerably more disruptive, being paranoid in nature, of spousal infidelity or family abandonment. Psychosis is an independent risk factor for nursing-home placement.[21]

Hallucinations can occur in parkinsonian syndromes for a variety of reasons. An overlap exists between PD and dementia with Lewy bodies, so that where Lewy bodies are present in the visual cortex, hallucinations may result. Hallucinations can also be brought about by excessive dopaminergic stimulation. Most hallucinations are visual in nature, often formed as familiar people or animals, and are generally not threatening in nature. Some patients find them comforting; however, their caregivers often find this part of the disease most disturbing, and the occurrence of hallucinations is a major risk factor for hospitalisation. Treatment options consist of modifying the dosage of dopaminergic drugs taken each day, adding an antipsychotic drug such as quetiapine, or offering caregivers a psychosocial intervention to help them cope with the hallucinations.

Sleep

Sleep problems can be worsened by medications for PD, but they are a core feature of the disease.[1] Some common symptoms are:

  • Excessive daytime somnolence[1]
  • Insomnia, characterized mostly by sleep fragmentation[1]
  • Disturbances in rapid eye movement sleep: disturbingly vivid dreams, and rapid eye movement behavior disorder, characterized by acting out of dream content:[1] It appears in a third of the patients and it is a risk factor for PD in the overall population.[1]

Perception

  • Impaired proprioception (the awareness of bodily position in three-dimensional space)
  • Reduction or loss of sense of smell (hyposmia or anosmia)[1] may be an early marker of the disease.[1]
  • Paresthesias[1]

Autonomic

  • Orthostatic hypotension[1] leading to dizziness and fainting
  • Oily skin[22]
  • Urinary incontinence[1] (typically in later disease progression) and nocturia (getting up in the night to pass urine)
  • Altered sexual function[1] is characterized by profound impairment of sexual arousal, behavior, orgasm, and drive, and is found in mid- and late PD.
  • Excessive sweating[1]

Gastrointestinal

Parkinson's Disease causes constipation and gastric dysmotility that is severe enough to endanger comfort and even health.[23] A factor in this is the appearance of Lewy bodies and Lewy neurites even before these affect the functioning of the substantia nigra in the neurons in the enteric nervous system that control gut functions.[24]

Neuro-ophthalmological

PD is related to different ophthalmological abnormalities produced by the neurological changes.[1][25] Among them are:

  • Decreased blink rate[1]
  • Irritation of the eye surface[1]
  • Alteration in the tear film[1]
  • Visual hallucinations[1]
  • Decreased eye convergence[1]
  • Blepharospasm[1]
  • Abnormalities in ocular pursuit, ocular fixation[26] and saccadic movements[1]
  • Difficulties to open the eyelids[1] This can have particular relevance when driving. People with Parkinson's have been shown to be less accurate in spotting landmarks and roadsigns whilst driving.[27]
  • Limitations in the upward gaze[1]
  • Blurred vision[25]
  • Diplopia (double vision), produced by a reduced eye convergence.[25]

References

1. ^1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 69 70 71 72 73 74 {{cite journal |author=Jankovic J |title=Parkinson's disease: clinical features and diagnosis |journal=J. Neurol. Neurosurg. Psychiatry |volume=79 |issue=4 |pages=368–76 |date=April 2008 |pmid=18344392 |url=http://jnnp.bmj.com/content/79/4/368.full|doi=10.1136/jnnp.2007.131045}}
2. ^1 {{cite book |vauthors=Cooper G, Eichhorn G, Rodnitzky RL |chapter=Parkinson's disease |editor=Conn PM| title=Neuroscience in medicine|publisher=Humana Press|location=Totowa |year=2008 |pages= 508–512|isbn=978-1-60327-454-8}}
3. ^{{cite book |vauthors=Banich MT, Compton RJ |chapter=Motor control | title=Cognitive neuroscience|publisher=Wadsworth, Cengage learning|location=Belmont, CA|year=2011 |pages= 108–44|isbn=978-0-8400-3298-0}}
4. ^{{cite book |vauthors=Fung VS, Thompson PD |chapter=Rigidity and spasticity |veditors=Tolosa E, Jankovic JJ | title=Parkinson's disease and movement disorders|publisher=Lippincott Williams & Wilkins |location=Hagerstown, MD |year=2007 |pages= 504–13|isbn=978-0-7817-7881-7}}
5. ^1 2 3 {{cite journal |vauthors=Samii A, Nutt JG, Ransom BR |title=Parkinson's disease |journal=Lancet |volume=363 |issue=9423 |pages=1783–93 |date=May 2004 |pmid=15172778 |doi=10.1016/S0140-6736(04)16305-8 }}
6. ^{{cite journal |vauthors=Rodriguez-Oroz MC, Jahanshahi M, Krack P, etal |title=Initial clinical manifestations of Parkinson's disease: features and pathophysiological mechanisms |journal=Lancet Neurol |volume=8 |issue=12 |pages=1128–39 |date=December 2009 |pmid=19909911 |doi=10.1016/S1474-4422(09)70293-5 |url=}}
7. ^{{cite journal |vauthors=Lepoutre A, Devos D, Blanchard-Dauphin A, etal |title=A specific clinical pattern of camptocormia in Parkinson's disease |journal=J. Neurol. Neurosurg. Psychiatry |volume=77 |issue=11 |pages=1229–34 |year=2006 |pmid=16735399 |doi=10.1136/jnnp.2005.083998 |pmc=2077366}}
8. ^{{cite journal |vauthors=Aarsland D, Brønnick K, Ehrt U, etal |title=Neuropsychiatric symptoms in patients with Parkinson's disease and dementia: frequency, profile and associated care giver stress |journal=Journal of Neurology, Neurosurgery, and Psychiatry |volume=78 |issue=1 |pages=36–42 |date=January 2007 |pmid=16820421 |pmc=2117797 |doi=10.1136/jnnp.2005.083113}}
9. ^1 2 {{cite journal|last1=Saeed|first1=U|last2=Compagnone|first2=J|last3=Aviv|first3=RI|last4=Strafella|first4=AP|last5=Black|first5=SE|last6=Lang|first6=AE|last7=Masellis|first7=M|title=Imaging biomarkers in Parkinson's disease and Parkinsonian syndromes: current and emerging concepts.|journal=Translational Neurodegeneration|date=2017|volume=6|issue=8|pages=8|pmid=28360997|pmc=5370489|doi=10.1186/s40035-017-0076-6}}
10. ^1 2 3 4 5 6 7 8 {{cite journal |vauthors=Caballol N, Martí MJ, Tolosa E |title=Cognitive dysfunction and dementia in Parkinson disease |journal=Mov. Disord. |volume=22 |issue= Suppl 17|pages=S358–66 |date=September 2007 |pmid=18175397 |doi=10.1002/mds.21677 |url=}}
11. ^{{Cite journal|pmid = 17987654|title = A systematic review of prevalence studies of depression in Parkinson's disease.|last = Reinders|first = JS|date = Jan 2008|journal = Movement Disorders|doi = 10.1002/mds.21803|volume=23|issue = 2|pages=183–9; quiz 313}}
12. ^{{cite journal |author = Lieberman A|title = Depression in Parkinson's disease -- a review|journal = Acta Neurologica Scandinavica|volume = 113|issue = 1|pages = 1–8|date = January 2006|pmid = 16367891|doi = 10.1111/j.1600-0404.2006.00536.x}}
13. ^{{cite journal |vauthors=Ishihara L, Brayne C |title=A systematic review of depression and mental illness preceding Parkinson's disease |journal=Acta Neurologica Scandinavica |volume=113 |issue=4 |pages=211–20 |date=April 2006 |pmid=16542159 |doi=10.1111/j.1600-0404.2006.00579.x}}
14. ^{{Cite journal|pmid = 25995056|title = Depression and subsequent risk of Parkinson disease: A nationwide cohort study.|last = Gustafsson|first = H|date = June 2015|journal = Neurology|doi = 10.1212/WNL.0000000000001684|volume=84|issue = 24|pmc=4478031|pages=2422–9}}
15. ^{{cite journal | author = McDonald W | last2 = Richard | first2 = IH | last3 = Delong | first3 = MR| title = Prevalence, Etiology, and Treatment of Depression in Parkinson's Disease | journal = Biol Psychiatry| volume = 54 | issue = 3| pages = 363–375 | year = 2003| pmid = 12893111| doi = 10.1016/S0006-3223(03)00530-4}}
16. ^{{Cite journal|title = Parkinson disease: Depression—risk factor or early symptom in Parkinson disease?|journal = Nature Reviews Neurology|pages = 432–433|volume = 11|issue = 8|doi = 10.1038/nrneurol.2015.126|pmid = 26215622|first = Albert F.|last = Leentjens|year=2015}}
17. ^{{Cite journal|title = Modeling depression in Parkinson disease Disease-specific and nonspecific risk factors|url = http://www.neurology.org/content/81/12/1036|journal = Neurology|date = 2013-09-17|issn = 0028-3878|pmc = 3795592|pmid = 23946309|pages = 1036–1043|volume = 81|issue = 12|doi = 10.1212/WNL.0b013e3182a4a503|first = Albert F. G.|last = Leentjens|first2 = Anja J. H.|last2 = Moonen|first3 = Kathy|last3 = Dujardin|first4 = Laura|last4 = Marsh|first5 = Pablo|last5 = Martinez-Martin|first6 = Irene H.|last6 = Richard|first7 = Sergio E.|last7 = Starkstein|first8 = Sebastian|last8 = Köhler}}
18. ^Menza, Matthew Combating Depression in Parkinson's Disease. Parkinson's Disease Foundation News & Review. Spring 2009.
19. ^Menza MA. Psychiatric symptoms associated with Parkinson disease. Drug Benefit Trends. 2010;22:58-60.
20. ^{{cite book | chapter=Non-motor features of Parkinson’s disease|editor=The National Collaborating Centre for Chronic Conditions | title=Parkinson's Disease | chapter-url=http://guidance.nice.org.uk/CG35/Guidance/pdf/English | publisher=Royal College of Physicians|location=London | year=2006 | isbn=978-1-86016-283-1 | pages=113–33 }}
21. ^{{cite journal |author=Friedman JH |title=Parkinson's disease psychosis 2010: A review article |journal=Parkinsonism Relat Disord |volume= 16|issue= 9|pages= 553–60|date=June 2010 |pmid=20538500 |doi=10.1016/j.parkreldis.2010.05.004 |url=}}
22. ^{{cite journal |vauthors=Gupta AK, Bluhm R |title=Seborrheic dermatitis |journal=Journal of the European Academy of Dermatology and Venereology |volume=18 |issue=1 |pages=13–26; quiz 19–20 |date=January 2004 |pmid=14678527 |doi=10.1111/j.1468-3083.2004.00693.x}}
23. ^{{cite journal |author=Pfeiffer RF |title=Gastrointestinal dysfunction in Parkinson's disease |journal=Lancet Neurology |volume=2 |issue=2 |pages=107–16 |date=February 2003 |pmid=12849267 |doi=10.1016/S1474-4422(03)00307-7}}
24. ^{{cite journal |vauthors=Lebouvier T, Chaumette T, Paillusson S, etal |title=The second brain and Parkinson's disease |journal=The European Journal of Neuroscience |volume=30 |issue=5 |pages=735–41 |date=September 2009 |pmid=19712093 |doi=10.1111/j.1460-9568.2009.06873.x}}
25. ^1 2 {{cite journal |author=Armstrong RA |title=Visual signs and symptoms of Parkinson's disease |journal=Clin Exp Optom |volume=91 |issue=2 |pages=129–38 |date=March 2008 |pmid=18271776 |doi=10.1111/j.1444-0938.2007.00211.x |url=}}
26. ^{{cite journal | pmid = 22490323 | doi=10.1001/archneurol.2012.70 | volume=69 | issue=8 | title=Pervasive ocular tremor in patients with Parkinson disease | year=2012 | author=Gitchel GT, Wetzel PA, Baron MS | journal=Arch Neurol | pages=1011–7}}
27. ^{{cite journal|author=Uc EY|last2=Rizzo|first2=M|last3=Anderson|first3=SW|last4=Sparks|first4=J|last5=Rodnitzky|first5=RL|last6=Dawson|first6=JD|title= Impaired visual search in drivers with Parkinson's disease|journal=Annals of Neurology|year=2006 | pages= 407–13|pmid=16969860|issue=4|doi= 10.1002/ana.20958|volume= 60}}

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