Wk2 - Polycystic Ovarian Syndrome (PCOS) and GI Flashcards

1
Q

What is PCOS?

A
  • one of most common hormonal problems in women during reproductive years

Polycystic = many cysts
- partially formed follicles on ovaries - each contain egg - rarely growth to maturity/be fertilised
- up to 1/3 women may have PCOS ovaries seen on ultrasound

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2
Q

How is PCOS Dx?

A
  1. irregular/absent periods
  2. acne, excess facial/body hair, scalp hair loss, high circulating androgen levels
  3. many small cysts on ovaries
  • don’t need ultrasound if you have 1. and 2.

For women aged <20y, ultrasounds not recommended

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3
Q

Please list the PCOS Sx?

A

Central obesity
- lean PCO ~30%

Irregular menstrual cycle
- periods may be less or more frequent due ot less frequent ovulation

Amenorrhoea
- some don’t menstruate - some cases… for many years

Excessive facial/body hair
Acne
Scalp hair loss
Reduced fertility - related to less frequent/absent ovulation
Sleep apnoea
Mental Health

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4
Q

What are the long-term health risks of PCOS?

A

~15y: clincial hyperandrogenism and Oligo-Anovulation

~25-30y: infertility, hyperandrogenism, pregnancy complication

~45y: hyperandrogenism, glucose intolerance

~55y: CV event, T2DM, endometrial cancer

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5
Q

What is PCOS associated with?

A
  • ~80% insulin resistance, risk of T2DM, esp. if overweight
  • CVD
  • pregnancy complications
  • blood lipid abnormalities
  • endometrial cancer
  • anxiety/depression
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6
Q

Why does PCOS increase risk for diabetes?

A

PCOS increases androgen levels = visceral adipose accumulation leading to increased inflammatory cytokines = insulin resistance and diabetes

  • too much insulin = inflammation causing weight gain, leading to T2DM and heart disease
  • high insulin is Sx of PCOS - impairs ovulation and causes ovaries to make excess testosterone
  • oral contraceptives -vely interfere with glycaemic control and insulin resistance
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7
Q

What is the prevalence of insulin resistance in obese and lean PCOS?

A

70-95% obese PCOS
30-75% lean PCOS

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8
Q

How is PCOS managed?

A

long-term management required
Includes:
* lifestyle mods - increase PA and healthy diet
* weight reduction - 5-10% loss provide significant health benefits
* med Tx - hormones or meds
* psychology - improve emotional health (mood, self confidence or body image)

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9
Q

What medications are used to manage PCOS?

A

Birth Control - regulate menstrual cycle, reduce excess hair growth, acne and prevent thickening of womb lining

Spirolactone - blocks hormones such as testosterone to reduce hair growth/scalp loss

Insulin sensitising meds (metformin) - improve insulin resistance, regulate menstrual cycles, ovulation and fertility, assist weight loss

Infertility meds - clomiphene citrate/aromatase inhibitors - stimulate ovulation

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10
Q

How is PCOS developed/caused?

A

Cause generally unknown

Genetics, hormones, lifestyle

Hypothalamic pituitary axis (HPA) imbalance

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11
Q

What is the prevalence of PCOS?

A

8-13% women of reproductive age
~50% cases unDx

Affects 1 in 10 women

50% with PCOS develop T2DM/pre-diabetes before 40y

4.3bill cost

3x increased risk of PCOS developing endometrial cancer

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12
Q

What are the risk factors of PCOS?

A

Family Hx - mum, aunt, sis with PCOS = 50% more likely

Race - more common in Asians, Aboriginal/TSI and African backgrounds

Others risks dependent on AGE…
* before birth (small gestational age)
*childhoold/prepuberty - early onset obesity, increased androgens during puberty onset, premature/pubarche, hyperinsulinaemai
* adolescence - obese, irregular menstrual/ olioamenorrhoea, polycystic ovarian morphology, high androgen levels, unwanted hair growth

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13
Q

What are the potential benefits of Ex?

A
  • insulin resistance
  • ovulation/reproductive health
  • conception
  • hirsutism/acne
  • cardiometabolic risk
  • mental health
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14
Q

What evidence is there of the potential benefit of Ex for PCOS?

A
  • 3M of supervised Ex improved insulin resistance despite weight maintenance
  • unlikely Ex elicits meaningful changes in HOMA-IR
  • benefits women with higher insulin resistance more
  • Ex w/wo diet = resumption of ovulation in overweight women by resetting HPA
  • Ex training improve rates (2x) clinical pregnancy and live births
  • equally effective as current drug Tx
  • Ex decreases hyperandrogenism - limited studies on hirsutism and acne
  • Improve CRF and waist circumference
  • SBP, lipid profiles unchanged
  • improve QoL, reduces Sx of depression/anxiety
    *RT effective = improves BGL, testosterone, sex hormone-binding globulin, strength, FFM
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15
Q

A patient asks “How will Ex benefit my health?”, what do you say?

A
  • increases occurrence of ovulation/conception
  • decreases cardiometabolic risk
  • improves mental health
  • decreases risk of diabetes
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16
Q

Please provide some Ex recommendations?

A

Lifestyle! increase PA and encourage healthy diet

  • encourage/advise prevention of weight gain/modest weight-loss, prevention of weight-regain
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17
Q

What would you tell someone with PCOS on whether training will improve chance of pregnancy?

A
  • lead to resumption in ovulation and increased rate of clinical pregnancy and live births
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18
Q

Provide a summary for PCOS.

A
  • common endocrine condition affecting up to 18% reproductive-aged women
  • associated with adverse reproductive, metabolic and psychological feature
  • benefits cardiometabolic comorbidities
  • evidence accumulating for Ex benefits on reproductive issues
  • PA guidelines
19
Q

What is the Gut-Brain Axis?

A

Bidirectional link between CNS and ENS
* involves in/direct pathways between cognitive/emotional centres with GI functions
* complex crosstalk between endocrine (HPA), immune (cytokine/chemokines) and ANS
*neuro-immuno-endocrine mediators of GBA allow brain to influence GI function (immune/epithelial cells, enteric neurons, smooth muscle cells)
* Cells of GI under influence of gut microbiota (important in GBA)

20
Q

Define gut microbiota.

A

Microbiome = all microorganisms in or on host and their genetic material
* approx 150x greater than human genome
* in gut, approx 10^14 microorganisms - ~10fold more cells than human body
* disruptions = alergies, autoimmune diseases, metabolic disorder nad neurpsychiatric disorders

Regular PA = modify intestinal microbiome, improve diversity and enhance no. of beneficial bacteria

21
Q

Provide some GI conditions.

A

STRUCTURAL
* IBD - ulcerative colitis // Crohn’s disease
* Gatroesophageal Reflux Disease (GORD)

FUNCTIONAL
* IBS // functional dyspepsia

  • Coeliac Disease
  • diverticulitis
  • Chronic Pancreatitis
    *Peptic Ulcer Disease
  • Lactose Intolerance
  • Eosinophilic GI Disorder (EGID)
22
Q

What is the difference between structural and functional GI conditions?

A

Structural:
Sx include nausea, abdominal pain, change in bowel habits with ABNORMAL physiology of 1 or more sections of GI tract
e.g. GORD, IBD, haemorrhoids, cancer

Functional:
Sx include nausea, abdombinal pain, change in bowel habits with NORMAL presentation of GI tract.
e.g. IBS, functional dyspepsia/dysphasia

23
Q

What is IBD?

A

Umbrella term for autoimmune disorder that leads to chronic inflammation of digestive tract.
2 main IBDs:
* ulcerative colitis - causes long-lasting inflammation and ulcers in innermost lining of large intestine and rectum
* Crohn’s Disease - inflammation of lining of digestive tract, often spread deep into affected tissues

24
Q

What happens when you have IBD?

A
  • involve severe diarrhea, abdominal pain, fatigue and weight loss
  • Dx in young adulthood ~25y, life-long disease
  • lead to comorbidities - rhumatoid arthritis, dermatological inflammation (rashes, eye disease) and lung conditions - emphysema

No known cause!

25
What is GORD?
* occurs when stomach acid frequently flows back into esophagus * acid reflux irritates esophagus lining * mild acid reflux occuring at least 2x/wk. Mod-sev = 1x/wk * can be managed with lifestyle and OTC meds * some require strong meds or surgery
26
What is ROME?
Use to categorise conditions. Adults: 8 domains and 22 sub-domains 5 most common subdomains: IBS, functional dyspepsia, functional constipation, function diarrhea & functional bloating/distention
27
What is IBS?
AKA nervous stomach, irritable colon * muscles of large intestine contract more often than normal * manage with diet, lifestyle and stress * abdominal pain relieved with bowel movement * more-sev Sx Tx with meds and couselling * IBS doesn't change bowel tissue or increase risk of colorectal cancer
28
Whatis Functional Dyspepsia?
* unexplained fullness after meals, unable to finish normal-sized meal, epigastric pain/burning * pain in uppder abdomen with bloating, belching and nausea * no obvious cause! * common / long-lasting * current Tx generally unsatisfactory due to lack of pathophysiological basis * when FD patients have postprandial fullness/early satiety - subclassed as postprandial distress syndrome (PDS) * with epigatsric burning/pain - subclassed as epigastric pain syndrome (EPS)
29
What is a low FODMAP diet?
"Fermented Oligosaccharides, Disaccharides, Monosaccharides And Polyols" * short-chain carbs not absorbed properly in gut * when in small intestine = move slowly, attracting water * when in large instine, fermented by gut bacteria, producing gas Extra gas + water = instestinal wall stretch and expand --> people with IBS causes exaggerated sensations of pain and discomfort
30
What is Coeliac disease?
Immune reaction in SI to eating gluten - a protein in wheat, barley and rye - over time, reaction damages SI lining, causes malabsorption - altered gut microbiota -may be responsible Causes: diarrhea, fatigue, weight loss, bloating and anaemia No CURE!! - follow strict GF diet to manage Sx and promote intestinal healing 1y after GF diet - more likely Dx with metabolic syndrome People with Celiac disease on GF diet rep high Tx burden (comparable with end-stage renal disease), up to 30% rep -ve Sx (GI upset) and sleep disturbances
31
What is diverticulitis?
* small, bulging pouches that can form lining of digestive system * commonly found in lower colon * common esp. >40y * when pouch/es become inflammed = diverticulitis Sx: * severe abdominal pain, fever, nausea and change in bowel habits Mild = Tx with rest, diet and antibiotics Sev/recurring = may requir surgery
32
What is the prevalence of GI conditions in AUS?
* 30% of adults >50 y havev GI complaint * IBD ~ 0.3% = 61,000 * 28,000 Crohn’s Disease * 33,000 Ulcerative Colitis * GORD ~ 15% * IBS ~ 20%, 2x more in women/younger individuals. * Coeliac Disease ~ 1.3% (1 in 70) // 80% remain unDx * Incidence 4-5fold over past 50y * Diverticular Disease - 5% in 40y/younger, 65% by 85y
33
What are the comorbidities of having GI tract condition?
Inflammatory Conditions – A ‘Flare-Up’ * reappearance of Sx * prescribe corticosteroids - reduce immune system to fight inflammation * usually avoid Ex during flare-up – dependant Sx * Mod Ex +vely modulates intestinal immune system while sev Ex is immunosuppressive Mental Health * High levels of poor mental health * Very prevalent in IBS, UC and FD Attributed to... * general psych stress of suffering from chronic/debilitating disease * derangement of GBA involving dysbiosis (microbial imbalance) impacting neurocognitive function.
34
What the hazards of Ex and general GI health?
Sx: nausea, heartburn, diarrhoea, GI bleeding common (20-40%) during Ex, esp. HIIT aerobic endurance activities (esp. long-distance running & triathlon) Sx: * transient, no long term consequences * progressive leading to cessation of Ex or decrease intensity. * Serious Sx limit Ex performance/participation Mechanisms of Ex causing GI Sx not well known: * decreased GI blood flow * increased GI motility * increased mechanical bouncing * altered neuroendocrine modulation
35
What are some GI health hazards from Ex based on evidence?
Single bout of long high intensity = gut damage/gut permeability damaged exacerbated in hot environments GI bleeding most serious Repeated GI bleeding = * iron deficiency and anaemia * endotoxaemia * malabsorption * GI inflammation Dehydration exacerbates condition
36
What are the benefits of Ex on general GI health?
* decrease risk of colon cancer * retrospective and prospective studies indicate Ex benefits disease course and QoL - reduces GI bleeding - inhibit appetite - functional capacity - general wellbeing by +ve mood changes - sleep - BMD
37
Explain the relationship between PA and IBD?
People with Crohn's Disease completed less mod-vig Ex than controls - long disease duration, low BMI, low VitD3 and inflammation evidenced by elevated serum C-reactive protein associated with low PA - Italisn study - 21% with IBD regularly Ex - Ex rates fluctuate with patient's disease activity
38
Why are some patients with IBD hesitant to seek Ex options and what is another main concern?
Ongoing GI Sx (e.g. diarrhea), may be hesitant Ex outside of home or in areas without bathroom access Sx exacerbation is another main concern. * 79% rep IBD limited participation * abdominal/joint pain, fatigue, flare-ups and increased fecal urgency * in healthy patients, strenuous, HIIT reduces blood flow to digestive system, can be exacerbated by hypovolaemia due to dehydration --> may be responsible of ischaemic colitis in HIIT endurance athletes (e.g marathoners and triathletes)
39
Was Ex responsive for IBD patients -- esp. British patient study?
72% rep Ex improved Sx 23% rep Ex exacerbated IBD symptoms: - 41% rep fatigue - 12% rep increased toilet needs - 17% rep abdominal pain - increase joint pain, IBD Sx and increased Rx time
40
What evidence of prospective studies demonstrate little danger of Sx exacerbation in people with IBD?
* 30mins cycling at 50% peak capacity and HIIT = similar increases in inflammatory markers between IBD and controls * all inflammatory markers returned to baseline within 60mins after Ex session * transient nature of elevations suggest little danger of Sx exacerbation Limited data suggest even HIIT is safe in selected IBD patients.
41
Explain the relationship between PA and GORD.
Cross-sectional Ex (>30mins, 3x/wk) -vely correlated with GORD No studies investigating an Ex intervention
42
Explain the relationship between PA and IBS.
Bowel movements more frequent and colon transit more rapid in PA individuals than sedentary * Systematic review of 14 RCT found * Ex is safe * GI Sx, QOL, anxiety, and IBS-related comorbidities = improvements with Ex compared to usual care * More research needed
43
Explain the relationship between PA and coeliac disease.
* 50% od low PA levels * metabolic bone disease = frequent co-morbidity * ~75% new Dx patients have low BMD and 40% greater risk of fractures * promote weight-bearing and resistance Ex
44
A client asks whether Ex will improve his Crohn's disease Sx. What would you say?
* People who are inactive will have more GI symptoms associated with their condition *Likely due to increased inflammation when people are sedentary * Unfortunately, there is little high level evidence for benefits of Ex on Crohns’s Disease * It is likely that the ‘right amount’ of exercise will create an anti-inflammatory environment that will improve GI symptoms and quality of life