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Journal of Clinical Endocrinology & Metabolism Vol. 70, No. 4 859-864
doi:10.1210/jcem-70-4-859
Copyright © 1990 by the Endocrine Society.
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Prevalence of {alpha}-Subunit Hypersecretion in Patients with Pituitary Tumors: Clinically Nonfunctioning and Somatotroph Adenomas*

DANIEL S. OPPENHEIM, ARNOLD R. KANA, JANGBIR S. SANGHA and ANNE KLIBANSKI

Neuroendocrine Unit and the General Clinical Research Center, Massachusetts General Hospital Boston, Massachusetts 02114

Address requests for reprints to: Anne Klibanski, M.D., Massachusetts General Hospital, Boston, Massachusetts 02114.

Hypersecretion of the pituitary glycoprotein hormone {alpha}-subunit has been reported in pituitary adenomas, particularly in clinically nonfunctioning tumors and somatotroph adenomas. However, the prevalence of such hypersecretion has not been precisely defined. Using both a new highly sensitive and specific monoclonal antibody assay and a polyclonal antibody assay, serum levels of free {alpha}-subunit were compared in 63 unselected patients with these tumors, 19 patients with acro-megaly, and 95 normal controls.

In all patients the monoclonal assay detected a significantly greater number of subjects with elevated {alpha}-subunit levels than did the polyclonal assay (21 vs. 14; P < 0.01). Fourteen of the 63 patients with clinically nonfunctioning tumors (22%) had elevated serum {alpha}-subunit levels in the monoclonal assay vs. 11 (17%) in the polyclonal assay. Among the 19 patients with acromegaly, the prevalence was 7 (37%) and 3 (16%) using the monoclonal and polyclonal assays, respectively.Twenty-eight (44%) of the patients with clinically nonfunctioning pituitary adenomas were female. Eleven (39%) of the women were under 45 yr old, as were 10 (29%) of the men.

We conclude that the prevalence of free {alpha}-subunit hypersecretion in patients with clinically nonfunctioning and somatotroph adenomas may be higher than previously recognized, and that a sensitive and specific monoclonal antibody free {alpha}-subunit assay may provide a useful tumor marker in these patients. The prevalence of clinically nonfunctioning pituitary tumors among younger men and women may also have been previously underestimated.

* This work was supported in part by NIH Grants DK-40947, RR-01066, and DK-07028.

Received June 13, 1989.




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