Muscle Dysfunction - Lecture 34 Flashcards

1
Q

How are sarcopenia and dynapenia different?

A

Dynapenia relates to muscle strength while sarcopenia relates to muscle mass

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2
Q

Which one takes more affect through aging? Dynapenia or Sarcopenia?

A

Dynapenia as neuromuscular changes counts for 90% of lost muscle strength.

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3
Q

Acute Muscle Soreness

A

Pain during or immediately after exercise

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4
Q

What are symptoms of acute muscle soreness

A
  • Accumulation of metabolic by-products (H+)
  • Tissue edema
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5
Q

What is tissue edema?

A

fluid shifting from blood plasma into tissues

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6
Q

DOMS (Delayed Onset Muscle Soreness)

A

24-48 hours post exercise and can last up to 3 days

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7
Q

Symptoms of DOMS

A
  • Tenderness
  • Range of motion limitation
  • Fatigue
  • Short terms losses in strength
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8
Q

What is DOMS caused by?

A

Inflammatory response to micro tears caused by High intensity resistance EX. (Not lactate buildup)

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9
Q

Who is DOMS most common among?

A

New exercisers or new stimulus

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10
Q

Misconception of DOMS

A

Need DOMS to occur for adaptation

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11
Q

Alleviating Symptoms for DOMS

A
  • Gentle Movement
  • Massage
  • Foam Rolling
  • Heat/Cold
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12
Q

How is DOMS preventable

A

Warm-up/Cool down & slow progression + hydration

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13
Q

Rhabdomyolysis

A

Striated Muscle Breakdown (Skeletal muscle)

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14
Q

What is Rhabdo Caused by?

A
  • Heavy strength training without rest
  • Injury/trauma
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15
Q

Symptoms of Rhabdo

A
  • Weakness
  • Dark Urine colour (proteins found in urine)
  • Muscle Swelling
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16
Q

Seriousness of Rhabdo

A

Can cause kidney failure & death

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17
Q

What is Rhabdomyolysis characterized as

A

Break down of muscle tissue

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18
Q

What happens internally during rhabdo?

A
  • Toxic components in circulation end up in kidneys
  • Myoglobin and proteins enter bloodstream
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19
Q

What’s an indicator of rhabdomyolysis

A

High levels of Creatine Kinase in the blood

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20
Q

Treatments for Rhabdomyolysis

A
  • IV Fluid
  • PT
  • Dialysis (if kidneys start to fail)
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21
Q

Relationship of Crossfit and Rhabdo

A

Culture that is glorifying a life threatening condition

22
Q

Fibromyalgia

A

Chronic Muscle Disorder

23
Q

How is Fibromyalgia characterized?

A
  • Widespread Pain
  • Fatigue, sleep disturbance
  • Cognitive issues
24
Q

Symptoms of Fibromyalgia

A
  • Migraine
  • IBS
  • Jaw Pain
  • Anxiety & Depression
25
Q

What happens when symptoms start for Fibromyalgia? (Symptom Onset)

A

Start to feel these “flare-ups” and they’re usually triggered by physical and psychological stressors

26
Q

Cause of Fibromyalgia

A

Repetition of nerve stimulation alters how brain senses pain

  • Amplifies pain
27
Q

What are some risk factors of getting Fibromyalgia?

A
  • Female
  • Family History
  • Osteoarthritis
28
Q

How is fibromyalgia diagnosed?

A

Diagnosis of exclusion

(Rules out everything it’s not and left with what it can be)

29
Q

What is a key factor in diagnosing fibromyalgia

A

Widespread pain in 4/5 areas of the body

  • Upper & Lower Left to Right Regions
  • Axial Region
30
Q

Treatment for Fibromyalgia

A

Mainly alleviation techniques

  • Stress reduction and exercise (restore functional ability)
31
Q

Muscle Dystrophy

A

A group of muscle diseases that are genetically inherited causing progressive muscle weakness

32
Q

Duchenne Muscular Dystrophy (DMD)

A
  • Most common form of muscle dystrophy
  • Inherited from mother
33
Q

What does DMD do internally?

A

Alters dystrophin protein expression (a protein used for building muscle)

34
Q

What happens when dystrophin is low?

A

Can’t replace and build new muscle fibres; fat accumulates

35
Q

Risk Factors of DMD

A
  • Males mostly
  • 2-6 years of age detected
  • Causes lung and heart issues
36
Q

Symptoms of DMD

A
  • Progressive muscle atrophy
  • Falls
  • Calf muscle hypertrophy
  • Cognitive impairment
  • Development Delay
37
Q

Diagnosis of DMD

A
  • 10-20X CK in blood
  • Genetic testing
  • Muscle biopsy
  • EKG
38
Q

Gower sign

A

An indicator where putting hands on knees before standing up

39
Q

Treatment for DMD

A

Maintaining what you have

  • Steroids
  • PT
  • Exercise
  • Mobility Aids
  • Cardiomyopathy
40
Q

What’s the end result of DMD

A

Wheelchair at 12 years
Life expectancy: 25-30

41
Q

ALS (Amyotrophic Lateral Scleorosis)

A

Neuromuscular disorder that affects motor neurons

42
Q

Damages in Upper motor neurons corresponds to…

A

Stiffness/spasticity

43
Q

Damage in Lower motor neurons corresponds to…

A

Atrophy/twitching

44
Q

Overtime effects of having ALS

A

Muscle atrophy & weakness along with loss of independence

45
Q

Prognosis (eventual death) of ALS is caused by what and on average how long?

A

Respiratory (3-5 years after diagnosis)

46
Q

Is ALS genetically inherited?

A

No; 90-95% are random

47
Q

Symptoms of ALS

A
  • Muscle weakness
  • Atrophy
  • Shortness of Breath
  • Frequent Chest Infections
  • Excess Saliva production
  • Stiffness
48
Q

When is ALS usually detected

A

55-75 among Caucasians

49
Q

Diagnosis of ALS

A
  • Neurological Exam
  • EMG Studies
  • Nerve conduction studies
50
Q

Treatment of ALS

A

Maintaining and maximizing what you have left

  • PT
  • Speech Therapy
  • Assistive devices
  • Pharmocotherapy