Blood Tests for Initial Evaluation of Pituitary Macroadenoma
For the initial evaluation of a pituitary macroadenoma, routine endocrine evaluation of all anterior pituitary axes is strongly recommended to assess for hypopituitarism and rule out hormone hypersecretion. 1
Comprehensive Pituitary Axis Testing
Growth Hormone (GH) Axis: Measure insulin-like growth factor 1 (IGF-1) to assess GH deficiency (present in 61-100% of patients) and to rule out clinically silent GH-secreting tumors 1
Gonadal Axis: Test luteinizing hormone (LH), follicle-stimulating hormone (FSH), testosterone in men, and estradiol in premenopausal women to identify central hypogonadism (present in 36-96% of patients) 1
Adrenal Axis: Measure morning cortisol and ACTH to detect adrenal insufficiency (present in 17-62% of patients), which requires replacement before surgery 1
Thyroid Axis: Test thyroid-stimulating hormone (TSH) and free T4 to identify central hypothyroidism (present in 8-81% of patients) 1
Prolactin: Measure serum prolactin to rule out hyperprolactinemia (present in 25-65% of patients) and to distinguish true nonfunctioning adenomas from prolactinomas 1
Clinical Significance and Rationale
The prevalence of overall hypopituitarism in patients with nonfunctioning pituitary macroadenomas ranges from 37% to 85%, with panhypopituitarism evident in 6% to 29% of patients 1
Identifying and treating adrenal insufficiency and significant hypothyroidism preoperatively is essential to reduce perioperative morbidity and mortality 1
Hyperprolactinemia in patients with macroadenomas may represent stalk effect rather than a true prolactinoma; levels typically remain below 200 ng/mL in nonfunctioning adenomas with stalk effect 1
Some apparently nonfunctioning adenomas may show immunostaining for hormones (particularly GH) despite lack of clinical symptoms, highlighting the importance of comprehensive testing 1
Important Considerations
Cutoff values to initiate thyroid and adrenal replacement might differ in patients with panhypopituitarism versus those with isolated deficiencies 1
Diabetes insipidus is uncommon at initial presentation (reported in only about 7% of patients), but should be considered if polyuria and polydipsia are present 1
No clinical evidence supports routine biomarker testing (e.g., α-subunit or chromogranin A) or genetic testing in patients with sporadic nonfunctioning pituitary adenomas 1
Mixed hormone-secreting tumors can occur, so comprehensive testing is necessary even when one hormone excess has been identified 2, 3