Table 1.

Causes of Hypoaldosteronism and Hormonal Profiles

Causes of HypoaldosteronismHormonal Profiles
DEFECTIVE STIMULATION OF ALDOSTERONE
❖ Congenital keep tablehyporeninemic hypoaldosteronism
❖ Acquired hyporeninemic hypoaldosteronism
Associated with diabetes mellitus
Associated with nephropathy
Glomerulonephritis
Gouty nephritis
Pyelonephritis
Nephropathy associated with multiple myeloma
Nephropathy associated with systemic lupus erythematosa
Mixed cryoglobulinemia
Nephrolithiasis
Analgesic nephropathy
Renal amyloidosis
Iga nephropathy
❖ Associated with autonomic insufficiency
❖ Associated with liver cirrhosis
❖ Associated with sickle cell anemia
❖ Associated with acquired immune deficiency syndrome
❖ Associated with polyneuropathy, organomegaly, endocrinopathy, m protein and skin changes syndrome
❖ Lead poisning
❖ Excess sodium bicarbonate
❖ Sjogren's syndrome
❖ Drugs interfering with renin production
Β-blocker
Prostaglandin synthetase inhibitors
Non-steroidal anti-inflammatory drugs
Calcium channel blocker
❖ Other drugs
Cyclosporin a
Mitomycin c
Cosyntropin
Low plasma renin;
Low plasma and urinary aldosterone
❖ Drugs interfering with angiotensin ii production
Angiotensin ii converting enzyme inhibitors
High plasma renin; low plasma aldosterone; low angiotensin ii
PRIMARY DEFECTS IN ADRENAL SECRETION OF ALDOSTERONE
❖ Combined with defective cortisol synthesis
a.

Congenital causes

Congenital adrenal hypoplasia (dax-1 mutation)
Congenital adrenal hyperplasia
-Cholesterol desmolase deficiency (lipoid adrenal hyperplasia)
-3β-hydroxysteroid dehydrogenase deficiency
-21-hydroxylase deficiency
-11β-hydroxylase deficiency
Adrenoleukodystrophy, adrenomyeloneuropathy
Low plasma renin; low plasma aldosterone; low plasma cortisol
High plasma deoxycorticosteorne
b) Acquired causes
Autoimmune adrenal destruction
-Addison's disease
-Multiple autoimmune endocrinopathy
Infectious adrenal destruction
-Bacterial infection
-Fungal infection
Infiltration of adrenal glands
-Amyloidosis
-Hemochromatosis
-Sarcoidosis
Metastatic or infiltrative malignant disease
Bilateral adrenalectomy
Drug induced
-Mitotane
-Aminoglutethimide
-Torilostane
-Ketoconazole
Low plasma renin; low plasma aldosterone; low plasma cortisol
❖ Isolated deficiency of aldosterone secretion

Congenital causes

-Cyp11b2 (aldosterone syntase) deficiency
-Corticosterone methyloxidase type i (cmo i) deficiency
-Corticosterone methyloxidase type ii (cmo ii) deficiency
High plasma renin; low plasma aldosterone
Normal plasma 18-hydroxycorticosterone/aldosterone ratio
High plasma 18-hydroxycorticosterone/aldosterone ratio

Acquired causes

Critically ill patients associated with hypotension or hypovolemia
-Sepsis
-Pneumonia
-Peritonitis
-Cholangitis
-Liver failure
After removal of mineralocorticoid secreting adrenal tumor
Discontinuation of agents with mineralocorticod activity
Heparin or chlorbutol administration
Low plasma aldosterone concentration; inappropriate elevated plasma renin
DEFECTIVE ALDOSTERONE ACTION
❖ Pseudohypoaldosteronism (pha) type 1
Renal (autosomal dominant pha)
Systemic pha (autosomal recessive pha)
❖ Secondary pseudohypoaldosteronism
Associated with urinary tract infection
Associated with medication that blocks epithelial sodium channel (enac)
-Amiloride
-Triamterene
-Trimethoprim
-Pentamidine
Administration of aldosterone antagonists
-Spironolactone
-Progesterone
-17-hydroxyprogesterone
-Synthetic progestin
Drugs that may lead to aldosterone resistance
-Caludinerin inhibitor (cyclosporin a, tacrolimus)
High plasma renin; high plasma and urinary aldosterone

From: Aldosterone Deficiency and Resistance

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Feingold KR, Anawalt B, Blackman MR, et al., editors.
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