Growth hormone and pituitary radiotherapy, but not serum insulin-like growth factor-I concentrations, predict excess mortality in patients with acromegaly.

Increased mortality in patients with acromegaly has been confirmed in a number of retrospective studies, but causative factors and relationship to serum IGF-I remain uncertain. The West Midlands Pituitary database contains details of 419 patients (241 female) with acromegaly. Serum IGF-I data from the Regional Endocrine Laboratory were available for 360 patients (86%). At diagnosis, mean age was 47 yr (range, 12-84) and mean duration of follow-up was 13 yr (0.5-48). Sixty-one percent were treated by surgery and 39% by nonsurgical means. Radiotherapy was used alone or as adjuvant therapy in 50%. All patients were registered with the Office of National Statistics to obtain information on deaths. At the date of analysis (31 December 2001), 95 of the 419 patients had died (43 males), giving a standardized mortality ratio of 1.26 [confidence interval (CI), 1.03-1.54; P = 0.046]. After controlling for age and sex, data indicated that mortality was increased in subjects with posttreatment GH levels more than 2 micro g/liter, compared with those with levels less than 2 micro g/liter [ratio of mortality rates (RR), 1.55 (range, 0.97-2.50); P = 0.068]. By contrast, a much smaller increase was observed for subjects with elevated posttreatment IGF-I levels compared with those with normal levels [RR, 1.20 (range, 0.71-2.03); P = 0.50]. Treatment with radiotherapy was associated with increased mortality [RR, 1.67 (range, 1.09-2.56); P = 0.018], with cerebrovascular disease the predominant cause of death [standardized mortality ratio, 4.42 (range, 2.71-7.22); P = 0.005]. These results confirm the increased mortality in acromegaly and suggest that reduction of GH levels to less than 2 micro g/liter is beneficial in terms of improving long-term outcome. The sole use of IGF-I as a marker for effective treatment of acromegaly is not justified by this data. This study also highlights the potential deleterious effect of radiotherapy.

[1]  D. Bonaduce,et al.  High prevalence of cardiac valve disease in acromegaly: an observational, analytical, case-control study. , 2003, The Journal of clinical endocrinology and metabolism.

[2]  J. Hardy,et al.  Long‐term outcome and mortality after transsphenoidal adenomectomy for acromegaly , 2003, Clinical endocrinology.

[3]  S. Ashley,et al.  Cerebrovascular mortality in patients with pituitary adenoma , 2002, Clinical endocrinology.

[4]  P M Stewart,et al.  Primary medical therapy for acromegaly: an open, prospective, multicenter study of the effects of subcutaneous and intramuscular slow-release octreotide on growth hormone, insulin-like growth factor-I, and tumor size. , 2002, The Journal of clinical endocrinology and metabolism.

[5]  P. Chanson,et al.  Guidelines for acromegaly management. , 2002, The Journal of clinical endocrinology and metabolism.

[6]  P. Stewart,et al.  Long-term safety and efficacy of depot long-acting somatostatin analogs for the treatment of acromegaly. , 2002, The Journal of clinical endocrinology and metabolism.

[7]  A. Barkan,et al.  Acromegaly with apparently normal GH secretion: implications for diagnosis and follow-up. , 2002, The Journal of clinical endocrinology and metabolism.

[8]  J. A. Scarlett,et al.  Long-term treatment of acromegaly with pegvisomant, a growth hormone receptor antagonist , 2001, The Lancet.

[9]  P. Cappabianca,et al.  Long-term effects of depot long-acting somatostatin analog octreotide on hormone levels and tumor mass in acromegaly. , 2001, The Journal of clinical endocrinology and metabolism.

[10]  J. Jenkins,et al.  Predictors of the outcome of surgical treatment in acromegaly and the value of the mean growth hormone day curve in assessing postoperative disease activity. , 2001, The Journal of clinical endocrinology and metabolism.

[11]  K. Wheatley,et al.  Association between premature mortality and hypopituitarism , 2001, The Lancet.

[12]  S. Yakar,et al.  The somatomedin hypothesis: 2001. , 2001, Endocrine reviews.

[13]  K. Wheatley,et al.  Association between premature mortality and hypopituitarism. West Midlands Prospective Hypopituitary Study Group. , 2001, Lancet.

[14]  F. Casanueva,et al.  Criteria for cure of acromegaly: a consensus statement. , 2000, The Journal of clinical endocrinology and metabolism.

[15]  S. Wardlaw,et al.  Evaluation of disease status with sensitive measures of growth hormone secretion in 60 postoperative patients with acromegaly. , 1998, The Journal of clinical endocrinology and metabolism.

[16]  P. Black,et al.  Long-term mortality after transsphenoidal surgery and adjunctive therapy for acromegaly. , 1998, The Journal of clinical endocrinology and metabolism.

[17]  Clark,et al.  Defining the normal cortisol response to the short Synacthen test: implications for the investigation of hypothalamic‐pituitary disorders , 1998, Clinical endocrinology.

[18]  R. McNally,et al.  Mortality and Cancer Incidence in Acromegaly: A Retrospective Cohort Study , 1998 .

[19]  S. Melmed,et al.  Journal of Clinical Endocrinology and Metabolism Printed in U.S.A. Copyright © 1998 by The Endocrine Society Current Treatment Guidelines for Acromegaly* , 2022 .

[20]  S. Shalet,et al.  Hypothalamic dysfunction in "cured" acromegaly is treatment modality dependent. , 1998, The Journal of clinical endocrinology and metabolism.

[21]  S. Orme,et al.  Mortality and cancer incidence in acromegaly: a retrospective cohort study. United Kingdom Acromegaly Study Group. , 1998, The Journal of clinical endocrinology and metabolism.

[22]  S. Mohan,et al.  Insulin-like growth factor-binding proteins in serum and other biological fluids: regulation and functions. , 1997, Endocrine reviews.

[23]  W. Heiss,et al.  Sleep apnoea in treated acromegaly: relative frequency and predisposing factors , 1996, Clinical endocrinology.

[24]  M. Wabitsch,et al.  The role of growth hormone/insulin-like growth factors in adipocyte differentiation. , 1995, Metabolism: clinical and experimental.

[25]  R. Clayton,et al.  Assessment of GH status in acromegaly using serum growth hormone, serum insulin‐like growth factor‐I and urinary growth hormone excretion , 1995, Clinical endocrinology.

[26]  P. Wrightson,et al.  Determinants of clinical outcome and survival in acromegaly , 1994, Clinical endocrinology.

[27]  A. Barkan,et al.  Persistence of rapid growth hormone (GH) pulsatility after successful removal of GH-producing pituitary tumors. , 1994, The Journal of clinical endocrinology and metabolism.

[28]  R. Clayton,et al.  An audit of outcome of treatment in acromegaly. , 1993, The Quarterly journal of medicine.

[29]  A. Barkan Acromegaly , 1890, Trends in Endocrinology & Metabolism.

[30]  J. Fraumeni,et al.  Acromegaly and gastrointestinal cancer , 1991, Cancer.

[31]  K. Ho,et al.  Contrasting effects of oral and transdermal routes of estrogen replacement therapy on 24-hour growth hormone (GH) secretion, insulin-like growth factor I, and GH-binding protein in postmenopausal women. , 1991, The Journal of clinical endocrinology and metabolism.

[32]  M. J. Dauncey,et al.  Variations in somatomedin-C/insulin-like growth factor-I associated with environmental temperature and nutrition. , 1990, Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme.

[33]  J. Flickinger,et al.  Incidence of cerebral infarction after radiotherapy for pituitary adenoma , 1989, Cancer.

[34]  R. Clayton,et al.  DOES GROWTH HORMONE RELEASING FACTOR DESENSITIZE THE SOMATOTROPH? INTERPRETATION OF RESPONSES OF GROWTH HORMONE DURING AND AFTER 10‐HOUR INFUSION OF GRF 1–29 AMIDE IN MAN , 1986, Clinical endocrinology.

[35]  D. Appleton,et al.  EPIDEMIOLOGY OF ACROMEGALY IN THE NEWCASTLE REGION , 1980, Clinical endocrinology.

[36]  C. Lowy,et al.  MORTALITY IN ACROMEGALY1 , 1970 .

[37]  C. Lowy,et al.  Mortality in acromegaly. , 1970, The Quarterly journal of medicine.