Trigger 3: Treatments and Diagnosis of Gordon's syndrome Flashcards

1
Q

patients with Gordon are suggested to…

A

have a low salt diet or take thiazide diuretics

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2
Q

surveillance includes..

A

routine electrolyte and BP measurement

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3
Q

Treatments aim to

A

keep BP low and electrolytes balanced

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4
Q

preventative

A

low salt diet

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5
Q

name 4 potential treatments for GS

A

1) Thiazide diuretics
2) Loop diuretics
3) SPAK inhibitors
4) WNK inhibitors

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6
Q

Thiazide diuretics: name two

A

chlorothalidone and metolazone

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7
Q

Thiazide diuretics basic mechanism

A
  • antagonist of the NCC Na/Cl transporter

- prevents the 10% sodium reabsorption which usually occurs in the DCT- preventing water absorption and lowering BP

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8
Q

Thiazide diuretics increase renal excretion of

A

sodium, potassium and hydrogen ion (metabolic alkalosis)

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9
Q

TDs decrease renal excretion of

A

Calcium

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10
Q

How to TDs work on a molecular basis

A

TDs compete for the chloride binding site on the Na/Cl cotransporter- inhibiting its ability to transport ions

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11
Q

Why do TDs decrease the renal excretion of calcium?

A

Inhibition of Na/Cl cotransporters lowers intracellular NA, which in turns results in lowering of intracellular calcium mediated by Na/Ca exchange expression basolateral membrane
- this facilitates the diffusion of calcium through calcium ion channels expressed on the lumen membrane

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12
Q

limitations of TDs

A

patients with WNK4 mutations respond better than those with WNK1 mutations
- cant take if urinanry problem, serve kidney or liver disease, addison disease

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13
Q

Loop diuretics

A

Inhibits NKCC2 symporters (LoH)

  • reducing osmotic force to drive reabsorption of water in the collecting duct
  • can cause hypokalaemia
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14
Q

Name two treatments in development

A

SPAK inhibitors and WNK inhibitors

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15
Q

SPAK inhibitors

A

SPAK kinases up regulate chloride influx through phosphorylation of NCC and NKCC2. In SPAK-knockout mice are hypotensive.

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16
Q

why could SPAK inhibitors be beneficial

A
  • would inhibit Cl- influx through both NCC and NKCC2

- wold avoid the side effect of hypokalaemia caused by T and L diuretics

17
Q

WNK inhibitors are

A

in clinical trials

18
Q

WNK inhibitors

A

would work by inhibiting the whole WNK-OSR-1/SPAK NCC cascade- reducing activation of NACL cotransporters, decreasing uptake of water and reducing BP.

19
Q

what is the proband

A
  • a particular subject being studied or reported on.
  • on pedigrees, the proband is noted with a square (male) or circle (female) shaded accordingly.
  • the proband is the first affected family member who seeks medical attention for a genetic disorder
20
Q

key diagnostic features (6)

A
  • hyperkalemia
  • normal GFR
  • hypertension
  • metabolic acidosis
  • hyperchloremia
  • suppressed plasma renin levels
  • low aldosterone
21
Q

genetic diagnosis

A

identification of heterozygous pathogenic variants.

22
Q

identification of heterozygous pathogenic variants… in which genes

A

CUL3, WNK1 or WNK4 or balletic pathogenic variants in KLHL3

23
Q

formal diagnostic criteria for PHAII

A

none published

24
Q

PHAII clinical feature manifest generally

A

in adolescence or adulthood

25
Q

Hypertension…

A

> 140/90

26
Q

metabolic acidosis

A

serum conc of bicarbonate ranging from 14-24mmol/l

27
Q

Hyperchloremia

A

serum conc of chloride ranging from 105 to 117 mol/L

28
Q

most PHAII cases are attributed to which pathogenic varianat

A

KLHL3 (41/86

29
Q

individuals with heterozygous CUL3 pathogenic variant tend to have ..

A

more severe hyperkalemia and metabolic acidosis, earlier development of hypertension and greater likelihood of growth impairment

30
Q

clinical manifestations tend to be milder in individuals with with heterozygous..

A

WNK1 or WNK4 pathogenic variants

31
Q

Biallelic

A

mutations in both alleles (not necessarily the same mutation)

32
Q

Individuals with balletic KLHL3 pathogenic variants

A

have more severe phenotypes than individuals with heterozygous pathogen variants in KLHL3

33
Q

Thiazide diuretics target

A

NCC cotransporters

34
Q

lopp diuretics target

A

NKCC1/2 cotransporters

35
Q

Gitelman syndrome caused by mutation in which cotransporter

A

NCC

36
Q

PHAII mutations on KLHL3 occur at

A

R528H

37
Q

PHAII mutations on CUL3 at

A

exon 9 deletion

38
Q

PHAII mutations on Wnk4 at

A

D561A