TY - JOUR
T1 - Gender and age in the biochemical assessment of cure of acromegaly
AU - Freda, Pamela U.
AU - Landman, Rita E.
AU - Sundeen, Robert E.
AU - Post, Kalmon D.
N1 - Funding Information:
Supported by NIH grant K08 DK02561 to PUF and RR-00645 to Columbia GCRC.
PY - 2001
Y1 - 2001
N2 - The principal biochemical criteria for cure in acromegaly are normalization of both glucose-suppressed GH levels and IGF-I levels. As we have reported previously, measurement of GH by highly sensitive assay in conjunction with IGF-I levels has led to a re-appraisal of "normal" GH suppression criteria during an OGTT in subjects with acromegaly. In some patients with active acromegaly, glucose-suppressed GH levels as measured by highly sensitive assay are much lower than could previously be appreciated with less sensitive GH assays and some other patients in apparent remission have subtle abnormalities of GH suppression. A question to arise is whether gender differences in glucose-suppressed GH levels as found by others in young healthy subjects should be considered in our interpretation of OGTT criteria for cure in acromegaly. Therefore, we have evaluated parameters of GH secretion in a larger number of subjects from our cohort of postoperative patients with acromegaly and in healthy subjects in order to determine if gender or age associated differences in these parameters exist. Ninety-two subjects with acromegaly (49 men, 43 women) and 46 age-matched healthy subjects (26 men, 20 women) were evaluated with baseline GH and IGF-I levels and nadir GH levels after a 100 g. OGTT. GH was assayed by highly sensitive IRMA (DSL). Basal GH levels were higher in female than in male healthy subjects, but the fall in GH from baseline (% suppression) was also greater in females resulting in no significant difference in mean nadir GH levels in female vs. male healthy subjects (0.09 vs. 0.08 μg/L). In the subjects with acromegaly, there were no significant gender differences in basal, % GH suppression or nadir GH levels. Basal and nadir GH levels correlated significantly only in subjects with active disease (r = 0.84, p < .0001). Similarly, IGF-I levels correlated significantly with basal (r = 0.573, p = .0012), and nadir (r = .702, p < .0001) GH levels only in subjects with active disease. Gender differences in IGF-I levels were not apparent in any group of subjects. As expected, IGF-I levels declined with age in those groups of subjects with normal IGF-I levels. Nadir GH levels did not vary with age. In conclusion, we have not found significant gender or age-related differences in nadir GH levels and thus our data does not support separate OGTT criteria for cure in men and women with acromegaly.
AB - The principal biochemical criteria for cure in acromegaly are normalization of both glucose-suppressed GH levels and IGF-I levels. As we have reported previously, measurement of GH by highly sensitive assay in conjunction with IGF-I levels has led to a re-appraisal of "normal" GH suppression criteria during an OGTT in subjects with acromegaly. In some patients with active acromegaly, glucose-suppressed GH levels as measured by highly sensitive assay are much lower than could previously be appreciated with less sensitive GH assays and some other patients in apparent remission have subtle abnormalities of GH suppression. A question to arise is whether gender differences in glucose-suppressed GH levels as found by others in young healthy subjects should be considered in our interpretation of OGTT criteria for cure in acromegaly. Therefore, we have evaluated parameters of GH secretion in a larger number of subjects from our cohort of postoperative patients with acromegaly and in healthy subjects in order to determine if gender or age associated differences in these parameters exist. Ninety-two subjects with acromegaly (49 men, 43 women) and 46 age-matched healthy subjects (26 men, 20 women) were evaluated with baseline GH and IGF-I levels and nadir GH levels after a 100 g. OGTT. GH was assayed by highly sensitive IRMA (DSL). Basal GH levels were higher in female than in male healthy subjects, but the fall in GH from baseline (% suppression) was also greater in females resulting in no significant difference in mean nadir GH levels in female vs. male healthy subjects (0.09 vs. 0.08 μg/L). In the subjects with acromegaly, there were no significant gender differences in basal, % GH suppression or nadir GH levels. Basal and nadir GH levels correlated significantly only in subjects with active disease (r = 0.84, p < .0001). Similarly, IGF-I levels correlated significantly with basal (r = 0.573, p = .0012), and nadir (r = .702, p < .0001) GH levels only in subjects with active disease. Gender differences in IGF-I levels were not apparent in any group of subjects. As expected, IGF-I levels declined with age in those groups of subjects with normal IGF-I levels. Nadir GH levels did not vary with age. In conclusion, we have not found significant gender or age-related differences in nadir GH levels and thus our data does not support separate OGTT criteria for cure in men and women with acromegaly.
KW - Acromegaly
KW - Growth hormone
KW - IGF-I
UR - http://www.scopus.com/inward/record.url?scp=0035557856&partnerID=8YFLogxK
U2 - 10.1023/A:1015314906972
DO - 10.1023/A:1015314906972
M3 - Article
C2 - 12138989
AN - SCOPUS:0035557856
SN - 1386-341X
VL - 4
SP - 163
EP - 171
JO - Pituitary
JF - Pituitary
IS - 3
ER -