This study was designed to examine the clinical characteristics of adult-onset growth hormone deficiency (AO-GHD) in patients aged over 65 years in comparison with patients aged less than 65 years. In addition, the effects of 12 months of GH replacement therapy on body composition, carbohydrate metabolism, blood pressure, serum lipids and quality of life were compared between patients aged over 65 years and patients under 45 years, 45–55 years and 55–65 years of age. The investigation was an observational study of patients enrolled in KIMS (Pharmacia International Metabolic Database). Baseline clinical characteristics were qualitatively similar, and scores from the Assessment of Quality of Life in GH-deficient Adults questionnaire (QoL-AGHDA) were indistinguishable between patients aged over 65 years and younger patients. Improvements in QoL-AGHDA scores were similar in all age groups during GH replacement therapy. Significant reductions in total and low-density lipoprotein cholesterol levels were observed in all groups and tended to be greater in patients aged over 65 years. Waist circumference and waist:hip ratio were not influenced by GH replacement therapy in women aged over 65 years, which was in contrast to the reductions observed in younger male and female patients and the decrease in waist circumference observed in men aged over 65 years. The similarities and differences in response to GH replacement therapy between patients aged over 65 years and those aged less than 65 years remained evident when the latter group was stratified by age. In conclusion, older patients with AO-GHD who receive GH replacement therapy achieve beneficial effects equivalent to those seen in younger patients in all age groups and require lower doses of GH.

The clinical features of growth hormone (GH) deficiency in hypopituitary adults and favourable responses to GH replacement therapy are now well recognized [1, 2, 3, 4, 5, 6, 7]. Normal ageing is associated with a progressive decline in spontaneous GH secretion, which appears to be, at least in part, related to an augmentation of somatostatinergic tone as acute GH responsiveness in elderly individuals is increased following administration of arginine [8, 9]. Furthermore, it has been suggested that some clinical features of ageing are similar to those of pathological GH deficiency (GHD) and might be directly attributable to this physiological relative GHD [10, 11, 12, 13]. Consequently, a number of studies have examined the effect of GH or GH-releasing hormone therapy on various clinical parameters in normal elderly people [14, 15, 16, 17, 18, 19, 20, 21, 22]. Generally, the effects of GH replacement therapy in these studies have only been of marginal benefit. The findings have raised three important questions regarding the clinical status of older hypopituitary patients. First, is it possible to diagnose GHD in older patients with pituitary disease in comparison with age-matched controls? Second, do older patients with GHD manifest phenotypic abnormalities that are distinct from those of normal ageing? Third, do older GH-deficient patients demonstrate beneficial effects from GH replacement therapy? Dealing with these in turn, it has been clearly documented that GH responses to both insulin-induced hypoglycaemia and intravenous arginine are decreased in elderly hypopituitary patients compared with age-matched controls [23, 24]. Furthermore, it has been shown that total and regional fat mass are increased in elderly hypopituitary patients compared with elderly control individuals [25]. More recently, preliminary studies, including data from KIMS (Pharmacia International Metabolic Database), have demonstrated improvements in the quality of life, body composition and lipoprotein profiles in hypopituitary adults aged over 60 years when given GH replacement therapy in comparison with normal elderly individuals [26, 27, 28]. These improvements are qualitatively similar to those observed in younger patients, but a detailed comparison with the responses stratified by age has not previously been reported. The aim of the present study, therefore, was to compare the clinical characteristics of all patients with adult-onset GHD (AO-GHD) aged over 65 years enrolled in KIMS with younger patients with AO-GHD. In addition, the effects of 12 months of GH replacement therapy on body composition, carbohydrate metabolism, blood pressure, serum lipids and quality of life were compared between patients aged over 65 years and patients aged less than 45 years, 45–55 years, and 55–65 years.

KIMS Outcomes Research Database

KIMS is a pharmacoepidemiological survey of adult GH-deficient patients treated with GH replacement therapy. At present, more than 8,000 patients from 26 countries are enrolled in KIMS. Following enrolment, patients are seen in local clinics at a frequency determined by the treating physician, with one visit per year being mandatory. At each visit, data are collected on specific case record forms and entered into a central database. Quality of data collection is monitored by clinical research representatives according to Good Clinical Practice Guidelines and the accuracy of data entry into the database is monitored by internal audit.


The analysis of baseline characteristics used information from 170 patients (103 men) with AO-GHD aged over 65 years commencing GH therapy at the time of enrolment into KIMS. Data were available for the effects of 12 months of GH therapy in 135 (83 men) of these patients. None of the patients had a previous history of acromegaly or Cushing’s disease. The data were compared with 1,395 patients (711 men) with AO-GHD aged less than 65 years enrolled in KIMS. Patients aged less than 65 years had not received GH therapy for at least 6 months before enrolment into the study and there was no previous history of acromegaly or Cushing’s disease. Patients were subdivided further into age groups of less than 45 years (n = 578), 45–55 years (n = 464) and 55–65 years (n = 353) of which 12-month treatment data were available for 476, 370 and 276 patients, respectively. GH replacement therapy was initiated at a maximum dose of 0.125 IU/kg/week (0.042 mg/kg/week) with a subsequent increase to a maximum of 0.25 IU/kg/week (0.083 mg/kg/week) based on individual responses. Within this maximum dosing guideline, the majority of patients were managed by dose titration against clinical response and serum insulin-like growth factor I (IGF-I) measurement. The aetiology and severity of GHD (peak GH and IGF-I standard deviation score [SDS]) in patients aged over and less than 65 years are provided in table 1.


Serum concentrations of IGF-I were measured by an HCl-extraction radioimmunoassay. Intra- and interassay coefficients of variation were less than 9% in the concentration range 125–1,046 µg/l.

Serum levels of total cholesterol were measured as described by Lie et al. [29], high-density lipoprotein (HDL) cholesterol was measured according to the method of Lopez-Virella et al. [30], and triglyceride levels were estimated by a hydrogen peroxide generation colorimetric method [31]. Serum low-density lipoprotein (LDL) cholesterol concentrations were calculated according to the Friedewald formula [32]. All serum IGF-I and lipid analyses were conducted in a single laboratory.

Blood pressure was measured supine after 5 min of rest. Waist and hip circumference measurements were conducted according to the KIMS guideline circulated to all participating clinics. Quality of life was assessed by the Assessment of Quality of Life in GH-deficient Adults questionnaire (QoL-AGHDA), a disease-sensitive, needs-based quality of life questionnaire which was developed specifically for adult GHD [33]. It has shown excellent reliability and cross-cultural comparability and has proven to be a sensitive means of monitoring changes in quality of life during long-term GH replacement therapy [7]. A higher QoL-AGHDA score, to a maximum of 25, indicates a poorer quality of life.

Statistical Analysis

Data analyses were performed using SAS (the Statistical Analysis System developed by the SAS Institute, USA). The significance of the effects of GH therapy was determined within each group by paired t tests, and between the groups by unpaired t tests if the data were normally distributed, and using Wilcoxon rank sum tests if they were not. Comparisons of proportions of various aetiologies and numbers of additional hormone deficiencies were performed using the Fischer exact and χ2 tests. Significance was accepted at p values of <0.05.

Baseline Characteristics

Details of aetiology, estimated duration of hypopituitarism, the number of additional pituitary hormone deficiencies, peak GH response to provocative stimulation, and baseline IGF-I SDS are provided in table 1. Adenoma was more common in patients aged over 65 years and craniopharyngioma was more common in younger patients. The diagnosis of GHD was made by insulin tolerance test in 55 and 51%, by arginine testing in 14 and 14%, by glucagon testing in 5 and 9%, and by other methods in 26 and 26% of patients aged over and less than 65 years, respectively. Mean peak serum GH level in response to provocative testing was significantly lower in female patients aged over 65 years compared with younger patients (p < 0.001), but mean peak serum GH concentrations in male patients older and younger than 65 years of age were similar. Peak serum GH levels were less than 3 ng/ml in 93 and 94% of patients aged less than and over 65 years, respectively. Serum IGF-I SDS was significantly higher in female patients aged over 65 years compared with younger patients, but the values in male patients were similar between the age groups. The duration of pituitary disease tended to be longer in patients aged over 65 years (p = 0.051).

Details of baseline waist:hip ratio, lipoprotein profiles, glycated haemoglobin (HbA1c), systolic and diastolic blood pressure, prevalence of hypertension and diabetes mellitus, and QoL-AGHDA scores are provided in tables 2 and 3. Prevalence of diagnosed hypertension was significantly higher in women aged over 65 years compared with younger women (p < 0.0001), but there was no significant difference between older and younger men. Similarly, the prevalence of diabetes mellitus was significantly higher in older women compared with the younger female patients (p < 0.002) with no significant difference between older and younger men. Older female patients demonstrated an increased body mass index and waist:hip ratio compared with the younger female patients. Mean levels of HbA1c were significantly higher in patients aged over 65 years compared with younger patients. Total and LDL-cholesterol were increased, and HDL-cholesterol was decreased in female patients aged over 65 years compared with younger women, but these differences were not evident in the male patients. As expected, systolic blood pressure was significantly higher in older male and female patients, but diastolic blood pressure was higher in the older male patients only. QoL- AGHDA scores were higher in the female patients than in the male patients, but were similar between the age groups.

Response to GH Replacement Therapy

Maintenance doses of GH at 12 months in the various age groups are shown in figure 1. The dose of GH was significantly lower in male and female patients aged over 65 years compared with the younger age categories, and the differential was greater in women (fig. 1).

Serum IGF-I SD scores are shown in figure 2. Mean IGF-I SDS was higher in female patients aged over 65 years than in younger female patients; in male patients, serum IGF-I SDS was higher in male patients aged 45–65 years compared with patients aged less than 45 years and over 65 years (fig. 2).

Waist Circumference

Waist circumference decreased in all age groups in both sexes (p < 0.001), but there were no differences in the degree of change in the waist circumference between the age groups (fig. 3).

Fasting Plasma Glucose and HbA1c

Mean fasting plasma glucose levels increased slightly in patients aged less than 65 years, but no significant increment was evident in older male and female patients (fig. 4). A parallel increment in HbA1c concentrations was seen in patients aged less than 65 years (fig. 4).

Systolic and Diastolic Blood Pressure

There was no significant change in systolic blood pressure in either sex across the age groups (fig. 5). In contrast, diastolic blood pressure fell significantly in women aged younger than 45 years (p < 0.003) and in men aged over 65 years (p < 0.05) compared with baseline data (fig. 6). Furthermore, the reduction in diastolic blood pressure was significantly greater in male patients aged over 65 years than in males aged less than 55 years and in females aged less than 55 years compared with women over 65 years (fig. 6).

Serum Lipoproteins

Serum total and LDL-cholesterol levels decreased during the 12 months of GH replacement therapy in both male and female patients in all age groups (p < 0.002). The decrease in LDL-cholesterol was significantly greater in men aged over 65 years compared with younger male patients, whereas in females, there were no significant changes across the age groups (fig. 7). There were no significant changes in levels of triglycerides or HDL-cholesterol in any group.

Quality of Life

QoL-AGHDA scores improved significantly from baseline (fig. 8) for both sexes in all age groups (females aged over 65 years, p < 0.001; females aged less than 65 years, p < 0.0001; males aged over 65 years and less than 65 years, p < 0.0001). However, there were no significant differences between the age groups for either sex (fig. 8).

The results of this analysis of KIMS data confirm our previous publication which examined the baseline characteristics and the response to 6 months of GH replacement therapy in elderly patients [27], and are concordant with the findings of previous single-centre studies [26, 28]. This study extends these findings by expanding the number of patients aged over 65 years and by stratifying the younger patients by age group as well as examining the response to GH replacement therapy over a 12-month period. Baseline clinical characteristics were qualitatively similar between the age groups and QoL-AGHDA scores in particular demonstrated a similar degree of impairment. However, older females, when compared with males, demonstrated a greater relative degree of adverse change in cardiovascular risk factors than younger patients of the same sex. All subgroups of patients had an equivalent degree of severe GHD on dynamic testing, as would be expected given the high prevalence of structural pituitary disease and severity of hypopituitarism. Although normal ageing is associated with a decline in spontaneous GH secretion, it is well established that it is possible to diagnose GHD by dynamic testing in older patients using similar criteria to those used in younger patients [23, 24].

The data for the dose of GH used and maintenance IGF-I concentration SDS are consistent with a dose-titration approach to GH replacement therapy. Favourable changes in waist circumference occurred in all groups and were of similar magnitude. The latter finding is in agreement with the previous demonstration of abnormal body fat and distribution in older hypopituitary adults compared with age-matched controls [25]. Furthermore, reductions in serum LDL-cholesterol levels were evident in all age groups, with the largest reduction in older male patients. These responses to GH therapy are more impressive than in our original report and are probably a reflection of the increased numbers of patients studied and, possibly, the longer duration of therapy [27]. We have again demonstrated that older patients experience a similar improvement in quality of life during GH replacement therapy and have extended this observation by confirming similar benefits gained in all stratified age groups of patients aged under 65 years.

GH replacement therapy is now widely used in GH-deficient adults, the majority of whom are middle aged at the start of therapy. This study provides unequivocal evidence that older GH-deficient adults obtain similar benefits to those observed in younger patients and argues for the use of GH therapy across the entire adult age range in patients with severe GHD. By inference, it is clear that the withdrawal of GH therapy in the ageing GH-deficient adult on the basis of an erroneous comparison with age-related physiological reduction in GH secretion in health is inappropriate.

We are grateful to our colleagues on the KIMS Strategic Scientific Committee and International Board and to the KIMS Investigators for their major contributions.

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