Endocrine Regulation of Male Fertility Flashcards

1
Q

What are the cells of the male reproductive system and what do they do? [3]

A
  1. spermatocytes
    • develop into sperm
  2. Leydig cells
    • secrete testosterone to promote sperm development
  3. Sertoli cells
    • blood-testis barrier
    • remove damaged spermatocytes
    • secrete androgen binding protein
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2
Q

What are the 2 molecules that most circulating testosterone is bound to? [2]

A
  1. sex-hormone binding globulin (SHBG)
  2. albumin
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3
Q

List the effects of testosterone on the body under the following headings:

  1. growth [5]
  2. adults [5]
  3. fertility [3]
  4. other effects [2]
A
  1. Growth
    • Sex organs
    • Skeletal muscle
    • Epiphyseal plates
    • Larynx growth
    • Secondary characteristics
  2. Adult
    • Muscle mass
    • Mood
    • Bone mass
    • Libido
    • Body shape
  3. Fertility
    • Libido
    • Erectile function
    • Spermatogenesis
  4. Other effects
    • Erythropoiesis
    • Behaviour
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4
Q

How is male gonadal function controlled? [8]

A
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5
Q

What are the clinical features of hypogonadism in children/young adults? [4]

A
  1. Slow growth in teens
  2. No puberty growth spurt
  3. Small testes & phallus
  4. Lack of secondary sexual development
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6
Q

What are the clinical features of hypogonadism in adults? [11]

A
  1. Depression/low mood
  2. Poor libido
  3. Erectile problems
  4. Poor muscle bulk/power
  5. Poor energy
  6. Sparse body/facial hair
  7. Gynaecomastia
  8. Gynoid weight gain
  9. Great head hair
  10. Short phallus
  11. Small testes - abnormal consistency
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7
Q

What are the tests used to investigate hypogonadism? [5]

A
  1. Sex steroid deficiency
  2. Testosterone
  3. LH & FSH
  4. Fertility
  5. Semen analysis
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8
Q

When is a semen analysis usually done and what are the normal figures? [5]

A
  1. 1-3 days after last ejaculation
  2. 2-5ml volume
  3. 20 x 106 sperm/ml
  4. 50% progressive motility
  5. ≥30% normal morphology
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9
Q

What are the general biochemical abnormalities associated with hypogonadotrophic hypogonadism? [7]

A
  1. Low testosterone
  2. Low LH +/- FSH
  3. +/- Increased prolactin
  4. +/- Decreased cortisol
  5. +/- Decreased IGF-1/GH
  6. +/- Decreased TSH
  7. +/- Increased Na+
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10
Q

What are the causes of hypopituitarism? [6]

A
  1. Pituitary tumour
  2. Pituitary surgery/radiotherapy
  3. Head injury
  4. Kallmann’s syndrome
    • Isolated LH & FSH deficiency
  5. Cerebellar ataxia
  6. Genetic syndromes
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11
Q

Describe the pathogenesis of Kallmann’s Syndrome and what conditions is it associated with? [4]

A
  1. Failure of cell migration of GnRH cells to hypothalamus from olfactory placode
  2. Associated with aplasia/hypoplasia of olfactory lobes — giving anosmia or hyposmia
  3. Also may be associated with deafness, renal agenesis, cleft lip/palate
  4. May have micropenis ± cryptorchidism
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12
Q

Describe the genetic basis of Kallmann’s Syndrome [5]

A
  1. Familial with variable penetration
  2. X-linked - absence of KAL gene (KAL1)
  3. Autosomal dominant (KAL2)
  4. Autosomal recessive (KAL3)
  5. Other genetic causes of IHH exist (e.g. Kisspeptin/GPR54 mutations)
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13
Q

What are the signs and symptoms of Kallmann’s Syndrome in…

  1. childhood? [2]
  2. adolescence? [4]
  3. adults? [4]
A
  1. Signs & Symptoms in Childhood:
    • Poor growth
    • Undescended testes
  2. Signs & Symptoms in Adolescence:
    • Poor growth
    • Small testes
    • Micropenis
    • Delayed/absent puberty features
  3. Signs & Symptoms in Adults:
    • Slow, but adequate growth
    • Small testes
    • Small phallus
    • Hypogonadal features
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14
Q

What are the causes of primary gonadal failure? [5]

A
  1. Klinefelter’s syndrome
    • Due to chromosome defects
  2. Complex genetic syndromes
  3. Cryptorchidism
  4. Adult Leydig Cell Failure & Seminiferous Tubule Failure
    • Can be caused by:
      • Trauma
      • Chemotherapy
      • Radiotherapy
      • Multisystem disorders
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15
Q

Describe the clinical pathogenesis of Klinefelter’s Syndrome [4]

A
  1. XXY (but other sex chromosome variations exist)
  2. Clinically manifests at puberty
  3. Increased ↑LH & FSH
    • but seminiferous tubules regress & Leydig cells don’t function normally
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16
Q

The clinical presentation of Klinefelter’s Syndrome is widely variable. What are the typical presenting features? [6]

A
  1. Delayed puberty
  2. Suboptimal genital development
  3. Reduced secondary male sexual characteristics
  4. Persistent gynaecomastia
  5. Azoospermia
  6. Behavioural issues/learning difficulties
17
Q

What are the management options for Klinefelter’s syndrome? [3]

A
  1. Androgen replacement +/-
  2. Psychological support +/-
  3. Fertility counselling
18
Q

What are the treatment options for hypogonadism? [5]

A
  1. Androgen replacement therapy
    • can be administered orally, IM or topical
  2. Fertility treatment
    • hCG
    • Recombinant LH & FSH
    • GnRH pumps
19
Q

What are the side effects of androgen replacement treatment? [6]

A
  1. Mood issues (aggression/behaviour change)
  2. Libido issues
  3. Increased haematocrit
  4. Possible prostate effects
  5. Acne, sweating
  6. Gynecomastia