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

被引:262
作者
Ayuk, J
Clayton, RN
Holder, G
Sheppard, MC
Stewart, PM [1 ]
Bates, AS
机构
[1] Univ Birmingham, Queen Elizabeth Hosp, Div Med Sci, Birmingham B15 2TH, W Midlands, England
[2] Univ Keele, Dept Postgrad Med, Stoke On Trent ST4 7QB, Staffs, England
[3] Birmingham Heartlands & Solihull Natl Hlth Serv T, Dept Endocrinol & Diabet, Birmingham B9 5SS, W Midlands, England
[4] Univ Hosp Birmingham NHS Trust, Reg Endocrine Lab, Dept Clin Biochem, Birmingham B29 6JD, W Midlands, England
关键词
D O I
10.1210/jc.2003-031584
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 mug/liter, compared with those with levels less than 2 mug/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 mug/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.
引用
收藏
页码:1613 / 1617
页数:5
相关论文
共 36 条
[1]   EPIDEMIOLOGY OF ACROMEGALY IN THE NEWCASTLE REGION [J].
ALEXANDER, L ;
APPLETON, D ;
HALL, R ;
ROSS, WM ;
WILKINSON, R .
CLINICAL ENDOCRINOLOGY, 1980, 12 (01) :71-79
[2]   Long-term safety and efficacy of depot long-acting somatostatin analogs for the treatment of acromegaly [J].
Ayuk, J ;
Stewart, SE ;
Stewart, PM ;
Sheppard, MC .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (09) :4142-4146
[3]  
BATES AS, 1993, Q J MED, V86, P293
[4]   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
[5]   Long-term outcome and mortality after transsphenoidal adenomectomy for acromegaly [J].
Beauregard, C ;
Truong, U ;
Hardy, J ;
Serri, O .
CLINICAL ENDOCRINOLOGY, 2003, 58 (01) :86-91
[6]   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 [J].
Bevan, JS ;
Atkin, SL ;
Atkinson, AB ;
Bouloux, PM ;
Hanna, F ;
Harris, PE ;
James, RA ;
McConnell, M ;
Roberts, GA ;
Scanlon, MF ;
Stewart, PM ;
Teasdale, E ;
Turner, HE ;
Wass, JAH ;
Wardlaw, JM .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (10) :4554-4563
[7]   Cerebrovascular mortality in patients with pituitary adenoma [J].
Brada, M ;
Ashley, S ;
Ford, D ;
Traish, D ;
Burchell, L ;
Rajan, B .
CLINICAL ENDOCRINOLOGY, 2002, 57 (06) :713-717
[8]  
Clark PM, 1998, CLIN ENDOCRINOL, V49, P287
[9]   High prevalence of cardiac valve disease in acromegaly: An observational, analytical, case-control study [J].
Colao, A ;
Spinelli, L ;
Marzullo, P ;
Pivonello, R ;
Petretta, M ;
Di Somma, C ;
Vitale, G ;
Bonaduce, D ;
Lombardi, G .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2003, 88 (07) :3196-3201
[10]   Long-term effects of depot long-acting somatostatin analog octreotide on hormone levels and tumor mass in acromegaly [J].
Colao, A ;
Ferone, D ;
Marzullo, P ;
Cappabianca, P ;
Cirillo, S ;
Boerlin, V ;
Lancranjan, I ;
Lombardi, G .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (06) :2779-2786