Laboratory Monitoring for Parathyroid Disorders
For parathyroid monitoring, measure serum calcium (corrected for albumin), intact parathyroid hormone (iPTH), serum phosphate, and 25-hydroxyvitamin D simultaneously, with monitoring frequency and additional tests determined by the specific clinical context (primary vs. secondary hyperparathyroidism, post-surgical monitoring, or chronic kidney disease). 1, 2, 3
Core Laboratory Panel
The essential tests for parathyroid monitoring include:
- Serum calcium (total calcium corrected for albumin) - This is the primary screening parameter and must be measured simultaneously with PTH for accurate interpretation 2, 3
- Intact parathyroid hormone (iPTH) using immunoradiometric assay (IRMA) or immunochemiluminometric assay (ICMA) - Required to distinguish primary from secondary hyperparathyroidism 3
- Serum phosphate - Typically low or low-normal in primary hyperparathyroidism, helps assess metabolic bone disease 2, 3
- 25-hydroxyvitamin D - Essential because vitamin D deficiency can complicate PTH interpretation and coexist with hyperparathyroidism 2, 3
Additional Essential Tests
Beyond the core panel, these tests provide critical information:
- Serum creatinine and blood urea nitrogen to assess kidney function, as hypercalcemia can cause kidney damage and chronic kidney disease causes secondary hyperparathyroidism 2, 3
- Serum albumin to correct total calcium values for accurate interpretation 3
- 1,25-dihydroxyvitamin D in select cases to further evaluate vitamin D metabolism 1, 3
- Alkaline phosphatase for additional information about bone turnover, though its predictive power is less established 3
Urine Studies
For comprehensive evaluation, particularly in primary hyperparathyroidism:
- 24-hour urine collection for calcium, creatinine, oxalate, uric acid, citrate, sodium, and potassium helps evaluate complications and metabolic abnormalities 3
- Random spot urine calcium/creatinine ratio to assess for hypercalciuria 2
- Urine calcium >400 mg/day on 24-hour collection identifies patients at increased risk for kidney stones and bone complications 3
Monitoring Frequency by Clinical Context
Secondary Hyperparathyroidism in Chronic Kidney Disease
For patients on dialysis or with CKD, monitoring frequency depends on disease stage and treatment status:
- When initiating or adjusting therapy: Measure serum calcium and phosphorus at least every 2 weeks for 1 month, then monthly for 3 months 3
- Once target levels are achieved: Monitor every 3 months 3
- For patients on cinacalcet: Measure iPTH no earlier than 12 hours after the most recent dose 4
- More frequent monitoring is needed in advanced CKD stages 3
Post-Bariatric Surgery
- Regular monitoring of PTH is recommended to evaluate for calcium and vitamin D deficiency 1
- PTH concentration >6.9 pmol/L (65 pg/mL) indicates calcium or vitamin D deficiency 1
Post-Thyroid Surgery
- Measure PTH 4 hours after surgery to predict postoperative hypoparathyroidism 1
- PTH concentration >1.6 pmol/L (15 pg/mL) measured ≥5 minutes after surgery indicates no need for intensive calcium monitoring 1
Primary Hyperparathyroidism
- Once maintenance dose is established: Monitor serum calcium approximately monthly 4
- For patients not on treatment: Monitor every 2 months 4
Critical Technical Considerations
PTH Assay Variability
Be aware that PTH assay differences can significantly affect clinical interpretation:
- Different assay generations measure different PTH fragments and isoforms in addition to biologically active PTH 1
- Lack of standardization leads to remarkable differences in PTH concentrations between laboratories 1
- Use assay-specific reference ranges for PTH measurement 2, 3
- Use the same PTH assay for all measurements in the same patient to ensure adequate trend evaluation 1
Sample Collection and Handling
- Collect blood in EDTA tubes for PTH measurement, as PTH is most stable in EDTA plasma 5
- Obtain blood samples in the morning after an overnight fast for optimal standardization 6
- Measure calcium on the same sample as PTH for correct interpretation 6
Common Pitfalls and How to Avoid Them
Vitamin D Status
Not assessing vitamin D status when interpreting PTH levels can lead to misdiagnosis:
- Vitamin D deficiency can suppress urine calcium excretion in primary hyperparathyroidism, potentially masking hypercalciuria 5
- Vitamin D deficiency can complicate interpretation of PTH levels and coexist with hyperparathyroidism 2, 3
- Low 25-hydroxyvitamin D is an expected finding in primary hyperparathyroidism, decreasing as serum calcium levels increase 7
Biotin Interference
Biotin supplements can interfere with PTH assays:
- Can cause falsely elevated or decreased results depending on the assay design 2, 3
- Patients should be asked about biotin supplementation before PTH testing 2
Interpreting PTH in Context
PTH must always be interpreted in relation to serum calcium:
- In primary hyperparathyroidism, PTH is elevated or inappropriately normal relative to the calcium level 1
- Normal or even low-normal PTH can still indicate primary hyperparathyroidism when calcium is elevated 7
- 10% of patients with surgically proven primary hyperparathyroidism had no high PTH values 7
Timing of Measurements
For patients on cinacalcet, timing matters:
- iPTH levels should be measured no earlier than 12 hours after the most recent dose 4
- This ensures accurate assessment of treatment effect 4
When to Consider Specialist Referral
Referral to a nephrologist and/or endocrinologist should be considered for: