Early postoperative indicators of late outcome in acromegalic patients

被引:22
作者
Takahashi, JA
Shimatsu, A
Nakao, K
Hashimoto, N
机构
[1] Kyoto Univ, Grad Sch Med, Dept Neurosurg, Sakyo Ku, Kyoto 6060857, Japan
[2] Kyoto Univ, Grad Sch Med, Dep Med & Clin Sci, Kyoto 6060857, Japan
[3] Kyoto Natl Hosp, Kyoto Clin Res Inst, Kyoto, Japan
关键词
D O I
10.1046/j.1365-2265.2003.01900.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE According to current criteria, normalised serum IGF-1 and glucose-suppressed GH < 1 ng/ml are indicators of biochemical cure in acromegalic patients. We performed a retrospective study to assess whether the attainment of these values in the early postoperative period was predictive of future IGF-1 normalisation and disease inactivity. PATIENTS, MEASUREMENTS AND RESULTS Between 1978 and 1999, 78 acromegalic patients underwent resection for pituitary adenomas. At the end of the mean follow-up period of 7 years, 43 (55.1%) showed normalised IGF-1 levels and no disease activity. In 51 cases, both IGF-1 and glucose-suppressed GH were examined within the first postoperative month. Of this group, all 19 patients who had early glucose-suppressed GH < 1 ng/ml and were treated by surgery alone maintained normal IGF-1 levels throughout the follow-up; four of them demonstrated delayed (i.e. more than 30 days after the operation) IGF-1 normalisation. In 19 patients with early glucose-suppressed GH levels of 1-4 ng/ml, seven of 11 patients with early normalised IGF-1 and two of eight patients with early IGF-1 elevation manifested eventual IGF-1 normalisation. However, none of the 13 patients with early glucose-suppressed GH > 4 ng/ml attained IGF-1 normalisation. Both univariate and multivariate analyses indicated that early glucose-suppressed GH was a significant factor for predicting late normalised IGF-1; the cut-off value was 1.5 ng/ml (sensitivity: 0.97; specificity: 0.75; odds ratio: 90). CONCLUSION The attainment of both normalised IGF-1 and glucose-suppressed GH < 1 ng/ml, even during the early postoperative period, suggests absolute cure in acromegalic patients. However, even in patients who do not meet both criteria within the first postoperative month, glucose-suppressed GH < 1.5 ng/ml, or glucose-suppressed GH < 4 ng/ml coupled with early IGF-1 normalisation indicate the possibility of eventual normalisation of IGF-1 and disease inactivity without adjuvant therapy. These postoperative parameters may be useful for assessing the desirability of further treatment.
引用
收藏
页码:366 / 374
页数:9
相关论文
共 54 条
[1]   Transsphenoidal microsurgery for growth hormone-secreting pituitary adenomas: Initial outcome and long-term results [J].
Abosch, A ;
Tyrrell, JB ;
Lamborn, KR ;
Hannegan, LT ;
Applebury, CB ;
Wilson, CB .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (10) :3411-3418
[2]   PLASMA INSULIN-LIKE GROWTH FACTOR-I/SOMATOMEDIN-C IN ACROMEGALY - CORRELATION WITH THE DEGREE OF GROWTH-HORMONE HYPERSECRETION [J].
BARKAN, AL ;
BEITINS, IZ ;
KELCH, RP .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1988, 67 (01) :69-73
[3]   Pituitary irradiation is ineffective in normalizing plasma insulin-like growth factor I in patients with acromegaly [J].
Barkan, AL ;
Halasz, I ;
Dornfeld, KJ ;
Jaffe, CA ;
Friberg, RD ;
Chandler, WF ;
Sandler, HM .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (10) :3187-3191
[4]   DOES TREATMENT OF ACROMEGALY AFFECT LIFE EXPECTANCY [J].
BATES, AS ;
VANTHOFF, W ;
JONES, JM ;
CLAYTON, RN .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1995, 44 (01) :1-5
[5]   ASSESSMENT OF GH STATUS IN ACROMEGALY USING SERUM GROWTH-HORMONE, SERUM INSULIN-LIKE GROWTH-FACTOR-I AND URINARY GROWTH-HORMONE EXCRETION [J].
BATES, AS ;
EVANS, AJ ;
JONES, P ;
CLAYTON, RN .
CLINICAL ENDOCRINOLOGY, 1995, 42 (04) :417-423
[6]  
BIERMASZ NR, 2000, J CLIN ENDOCRINOLOGY, V85, P2467
[7]  
BIERMASZ NR, 2000, J CLIN ENDOCRINOLOGY, V85, P4569
[8]   The incidence of cerebrovascular accidents in patients with pituitary adenoma [J].
Brada, M ;
Burchell, L ;
Ashley, S ;
Traish, D .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1999, 45 (03) :693-698
[9]  
CLAYTON RN, 1997, J ENDOCRINOL, V155, P23
[10]  
Collins WF., 1979, CLIN MANAGEMENT PITU, P335