Disorders of Calcium Metabolism Flashcards
Calcium distribution
- Bones & teeth (~99%)
- ICF (~1%)
- ECF (<1%)
Calcium Sensor Receptor activation effects
Parathyroid Cell -PTH Secretion Parafollicular C-Cell -Calcitonin Secretion Renal Tubular Cell -Calcium Excretion
Primary Hyperparathyroidism Classification
- Adenoma85%
- Hyperplasia15%
- Carcinoma< 1%
Primary Hyperparathyroidism Clinical Features
-Asymptomatic (> 50%)
-Skeletal Disease
-Kidney Disease
-Gastrointestinal Disease
-Psychiatric Disease
-Band Keratopathy
(Bones Stones Groans Moans)
Signs of Hyperparathyroidism
- Brown Tumor (Osteoclastoma)
- Osteitis Fibrosa Cystica
- Chondrocalcinosis
- Band Keratopathy
Lab findings in Primary Hyperparathyroidism
Inc Serum Calcium
Dec Serum Phosphate
Inc Serum PTH
Genetic causes of Primary Hyperparathyroidism
Sporadic90% Familial10% -Familial HPT -MEN I -MEN IIA
MEN 1 features & mutation
- Pituitary tumors
- Pancreatic Islet Tumors
- Parathyroid Hyperplasia
- Germline Mutation: Menin Gene
MEN 2a features & mutation
- Medullary Thyroid Carcinoma
- Pheochromocytoma
- Parathyroid Hyperplasia
- Germline mutation: RetGene (GDNF receptor)
Primary Hyperparathyroidism Treatment
- Surgery
- CalcimimeticDrug (Cinacalcet)
- Anti-ResorptiveBone Drug (Bisphosphonate, Denosumab)
Most common causes of hypercalcemia
- Primary Hyperparathyroidism
2. Hypercalcemia of malignancy
WHEN DO you find increased PTH
FHH & primary hyperparathyridism
Hypercalcemia of Malignancy Mediators
PTH Related Peptide (PTH-RP)
Lab findings in Hypercalcemia of Malignancy
Inc Serum Calcium
Low Serum PTH
Inc Serum PTH-RP
Familial Hypocalciuric Hypercalcemia lab findings
Inc Serum Calcium (mild)
High Serum PTH (mild)
Low Urinary Calcium (defective receptor/excretion in kidney)
Low Urine Calcium / Creatinine Clearance Ratio
Hypocalcemia Causes
Vitamin D Deficiency Hypoparathyroidism (only one w/ low PTH) Pseudohypoparathyroidism Hypomagnesemia Hypoproteinemia**
Corrected Serum Total Calcium method
Add 0.8 mg/dl to total Calcium for every 1 g/L Albumin is < 4.0 g/L
Hypocalcemia Clinical Features
Paresthesias Muscle Cramps Muscle Weakness Chvostek’s Sign Trousseau’s Sign
Major Storage Form of Vitamin D
25 OH Vitamin D
Vitamin D Disorders
- Acquired Vitamin D Deficiency (Intake probs, no sun)
- Acquired 1,25 (OH)2 Vitamin D Deficiency (Renal Disease Hypoparathyroidism)
- Congenital 1 Alpha Hydroxylase Deficiency “Vitamin D Dependent Rickets Type 1”
- Congenital Vitamin D Receptor Deficiency “Vitamin D Dependent Rickets Type 2”
Nutritional Vitamin D Deficiency Lab findings
Low Serum Calcium low Serum Phosphate highSerum Alkaline Phosphatase high Serum PTH low Serum 25 (OH) Vitamin D low urine Calcium
Clinical features of Vit D deficicny
Osteomalacia –Pseudofracture
Hypoparathyroidism Laboratory Features
Low Serum Calcium
High Serum Phosphate
Low Serum PTH
Pseudohypoparathyroidism Causes
Inactivating mutation of the GS alpha subunit or other downstream PTH response element
Pseudohypoparathyroidism Laboratory Features
- low Serum Calcium
- high Serum Phosphate
- high Serum PTH
- Short 4th + 5th Metacarpals (Albright’s Hereditary Osteodystrophy)