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An acromegalic patient with recurrent urolithiasis

Endocrinologia Japonica
|December 1, 1985
PubMed

Insights

Acromegaly, a condition caused by excess growth hormone (GH), can lead to elevated vitamin D levels and kidney stones. Treating the underlying cause improved these metabolic abnormalities.

Area of Science:

  • Endocrinology
  • Nephrology
  • Metabolic Disorders

Background:

  • Acromegaly is characterized by excessive growth hormone (GH) production, leading to various systemic complications.
  • Urolithiasis, or kidney stones, is a known complication, often linked to hypercalciuria.

Observation:

  • A patient with acromegaly presented with abdominal pain and hematuria due to urolithiasis.
  • Investigations revealed hypercalciuria and elevated serum 1,25-dihydroxyvitamin D (1,25-(OH)2D) levels, ruling out hyperparathyroidism.
  • Serum calcium and parathyroid hormone (PTH) levels were within normal limits.

Findings:

  • Selective adenomectomy to treat the acromegaly normalized 1,25-(OH)2D levels and resolved hypercalciuria and urolithiasis.
  • Pre-operative 1,25-(OH)2D levels were significantly elevated (55.0 and 73.0 pg/ml) compared to the normal range (27.2-53.8 pg/ml).
  • Post-operative 1,25-(OH)2D levels decreased to 23.0 pg/ml.

Implications:

  • Growth hormone (GH) may stimulate vitamin D activation in the kidneys in acromegaly patients.
  • This increased vitamin D activation enhances intestinal calcium absorption and urinary calcium excretion.
  • Targeting GH excess can effectively manage vitamin D-related metabolic disturbances and urolithiasis in acromegaly.

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