Determinants of clinical outcome and survival in acromegaly
- 1 July 1994
- journal article
- Published by Wiley in Clinical Endocrinology
- Vol. 41 (1) , 95-102
- https://doi.org/10.1111/j.1365-2265.1994.tb03789.x
Abstract
Summary: OBJECTIVE The extent to which treatment modifies the excess in morbidity and mortality in acromegaly remains uncertain. This study investigates the determinants of final outcome following therapy for acromegaly. DESIGN A retrospective analysis of patients treated at the Departments of Endocrinology and Neurosurgery, Auckland Hospital, New Zealand.PATIENTS One hundred and fifty‐one patients (63 females and 88 males) with acromegaly or gigantism treated between the years 1964 and 1989. The mean duration of follow‐up was 12 years (median 11 years).MEASUREMENTS Patients had their age, estimated duration of symptoms preceding diagnosis, serum GH at diagnosis, presence of diabetes mellitus, cardiovascular disease, hypertension and/or osteoarthritis at diagnosis and the last known serum GH documented. The final outcome at the time of study was graded under three classes: dead (n = 32), those with major complications (n =47) and those with minor/no complications (n = 67).RESULTS The mean age at diagnosis of acromegaly was 41 years and the average estimated duration of symptoms prior to diagnosis was 7 years, with older patients showing longer duration of symptoms preceding diagnosis (P= 0.0002). Final outcome (dead, alive with major complications, alive and well) was significantly worse in those with older age at diagnosis (P= 0.008), longer duration of symptoms before diagnosis (P= 0.03) and higher GH at last follow‐up (P=0.0001). In multivariate analysis, survival was significantly Influenced by the last known GH (P = 0.0001), presence of hypertension (P = 0.02) or cardiac disease (P = 0.03) at diagnosis, and duration of symptoms prior to diagnosis (P = 0.04). Survival In the acromegalic group, irrespective of treatment, was reduced by an average of 10 years compared with the non‐acromegalic population.CONCLUSIONS Acromegaly has a significant adverse effect on well‐being and survival. The predominant determinant of outcome is the final serum GH level following treatment.Keywords
This publication has 20 references indexed in Scilit:
- Inter‐relations between growth hormone, insulin, insulin‐like growth factor‐l (IGF‐I), IGF‐binding protein‐1 (IGFBP‐1) and sex hormone‐binding globulin in acromegalyClinical Endocrinology, 1991
- Sequelae to Acromegaly: Reversibility with Treatment of the Primary DiseaseHormone and Metabolic Research, 1990
- Evaluation of selective transsphenoidal adenomectomy by endocrinological testing and somatomedin-C measurement in acromegalyJournal of Neurosurgery, 1989
- Epidemiology and Long‐term Survival in Acromegaly: A Study of 166 Cases Diagnosed between 1955 and 1984Acta Medica Scandinavica, 1988
- ACROMEGALYClinical Endocrinology, 1987
- STUDIES OF INSULIN‐LIKE GROWTH FACTOR ‐I AND ‐II BY SPECIFIC RADIOLIGAND ASSAYS IN UMBILICAL CORD BLOODClinical Endocrinology, 1983
- EPIDEMIOLOGY OF ACROMEGALY IN THE NEWCASTLE REGIONClinical Endocrinology, 1980
- Nonparametric Estimation from Incomplete ObservationsJournal of the American Statistical Association, 1958
- Nonparametric Estimation from Incomplete ObservationsJournal of the American Statistical Association, 1958