Abstract
PurposePostoperative assessment of acromegaly activity is typically performed at least 3 months after neurosurgery (NS). Few studies have evaluated the use of early postoperative growth hormone (GH) levels as a test to predict short- and long-term remission of acromegaly. Our objective was to evaluate the diagnostic performance of serum random GH on a postoperative day one (D1-rGH) and two (D2-rGH), particularly in predicting long-term disease persistence.Materials and methodsForty-one subjects with acromegaly who were undergoing NS were enrolled (mean age ± SD 47.4 ± 13.1 years at diagnosis; women 54%; macroadenomas 71%). The final assessment of disease activity was performed one year after NS. ROC curves were used to evaluate the diagnostic performance of D1-rGH and D2-rGH.ResultsAfter a 1-year follow-up, the overall remission rate was 55%. ROC analysis identified an optimal D1-rGH cut-off value of 2.1 ng/mL for diagnosing long-term disease persistence (55.6% SE; 90.9% SP). The cut-off point became 2.5 ng/mL after maximizing specificity for disease persistence (yielding a 100% positive predictive value) and 0.3 ng/mL after maximizing sensitivity for disease remission. The optimal D2-rGH cut-off value was 0.6 ng/mL (81.8% SE; 50% SP); the cut-off point became 2.9 ng/mL after maximizing specificity and 0.1 ng/mL after maximizing sensitivity, with no clinical utility.ConclusionsD1-rGH could be a highly specific test for the early diagnosis of long-term acromegaly persistence, which is predicted by a value > 2.5 ng/mL with a great degree of certainty. The diagnostic performance of D2-rGH was insufficient. Further research is required to validate these preliminary results prior to modifying the postoperative management of acromegaly.
Highlights
Neurosurgery (NS) is considered the first choice to cure acromegaly
All surgical procedures were performed by a single neurosurgeon dedicated to pituitary surgery (FZ), using a 3D endoscopic endonasal approach; only one patient needed a combined transcranial and endonasal approach due to a “supergiant” growth hormone (GH)-secreting pituitary adenoma [10]
All patients were affected by a GH-secreting pituitary adenoma (71% macroadenomas) with a median diameter of 12 mm (8 − 21)
Summary
Neurosurgery (NS) is considered the first choice to cure acromegaly. The remission rate is variable (56 − 72%) depending on the clinical center and operator [1]. Technical progress has improved surgical outcomes to achieve a post-NS remission rate of 60 − 85% in the largest cohorts [3, 4]. Re-evaluation of the disease state after NS is typically performed by measuring IGF1 and nadir GH after an oral glucose tolerance test (OGTT) at least 12 weeks post-intervention due to the long half-life of IGF1 [2, 5]. The American Association of Clinical Endocrinologists (AACE) guidelines for acromegaly recommend that “a fasting GH level be measured early postoperatively” to predict
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