Abstract
Purpose
To examine differences in effects according to growth hormone (GH) treatment duration in adult GH-deficient patients.
Methods
In the Italian cohort of the observational Hypopituitary Control and Complications Study, GH-treated adults with GH deficiency (GHD) were grouped by duration of treatment; ≤ 2 years (n = 451), > 2 to ≤ 6 years (n = 387) and > 6 years (n = 395). Between-group differences in demographics, medical history, physical characteristics, insulin-like growth factor-I standard deviation score (IGF-I SDS) and lipid profile at baseline, last study visit and changes from baseline to last study visit were assessed overall, for adult- and childhood-onset GHD and by gender using ANOVA for continuous variables and Chi-squared test for categorical variables.
Results
At baseline, treatment duration groups did not differ significantly for age, gender, body mass index, GHD onset, IGF-I SDS, lipid profile, and quality of life. Mean initial GH dose did not differ significantly according to treatment duration group in any subgroup, except female patients, with highest mean dose seen in the longest duration group. In the longest duration group for patients overall, adult-onset patients and male patients, there were significant decreases in GH dose from baseline to last visit, and in total and low-density lipoprotein (LDL)-cholesterol concentrations. IGF-I SDS increased, to a greater extent, in the longest duration group for patients overall and female patients.
Conclusions
The results show that long-term GH treatment is associated with decreasing GH dose, increased IGF-I, decreased LDL-cholesterol and the presence of surrogate markers that help to give confidence in a diagnosis of GHD.
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Introduction
Growth hormone (GH) deficiency in adult patients is associated with increased risk of mortality, predominantly due to cardiovascular disease [1,2,3,4]. GH-deficient patients frequently have excess body fat, decreased lean body mass and an abnormal lipid profile, and GH treatment is able to reverse these effects [2,3,4,5,6,7,8]. Adult patients diagnosed as having GH deficiency require continuous treatment with GH throughout their lives to maintain the metabolic benefits. However, the effects of such continuous GH treatment may change over time and data are required to evaluate such potential changes.
Data from large observational studies indicate that duration of GH treatment varies widely from a few months to many years. However, only limited data have been published that enable comparison of metabolic and hormonal effects between short-term versus long-term GH treatment [8, 9]. In the observational Hypopituitary Control and Complications Study (HypoCCS) programme, data have been collected for a large number of adult patients with GH deficiency who were treated with GH [10, 11]. Among the 16 countries in Europe and North America that enrolled patients into HypoCCS, Italy was a major contributing country to the database [12]. The present analysis used the Italian cohort of patients in HypoCCS, which included data from patients with various durations of GH treatment. The present analysis was carried out to examine differences in baseline characteristics, efficacy and quality of life between patients who received GH treatment for different durations, to investigate changes in effects during short-term versus long-term treatment.
Methods
Patients and study design
HypoCCS was a multi-national surveillance study designed to examine the safety and efficacy of long-term GH treatment in adult patients with GH deficiency. Patients entered into the study were adults, aged at least 18 years, with onset of GH deficiency either during childhood (CO) or adulthood (AO). Because HypoCCS was a surveillance study, the diagnosis of GH deficiency, entry into the study and all treatment decisions were at the discretion of the attending physician according to local guidelines. The Italian cohort of patients who entered into the present analysis met the criteria for the indication of adult treatment with GH, according to Italian reimbursement rules described in Nota AIFA no. 39.
Other than a diagnosis of GH deficiency, the only inclusion criterion for entry to HypoCCS was that patients had achieved adult height, with closed epiphyses. Exclusion criteria included active malignancy, recent growth of a pituitary adenoma or other intracranial tumour, presence of acute critical illness due to complications following open heart or abdominal surgery, multiple accidental traumas, or acute respiratory failure.
HypoCCS was registered with ClinicalTrials.gov, study number NCT01088399. The clinical study protocol was approved by appropriate institutional review boards and adhered to all applicable regulatory requirements. All patients provided signed informed consent for data collection, electronic processing and publication, in accordance with national laws. The study was performed according to the ethical principles of the Declaration of Helsinki.
Study evaluations
Data collected at baseline and during follow-up included demographics, medical history, height, weight, body mass index (BMI), insulin-like growth factor-I (IGF-I) concentrations, lipid profile and Framingham cardiovascular risk index. Study visits for clinical assessment occurred at approximately 6- to 12-month intervals, although time between visits was flexible, in line with clinical practice.
Peak GH concentration following stimulation testing was determined at local laboratories using commercially available GH assays. IGF-I concentration was measured at a central laboratory (IGF Labor, Universitats Kinderklinik, Giessen, Germany) and values were converted to standard deviation scores (SDS) based on age- and gender-matched reference ranges, using published methods [13]. Concentrations of total cholesterol, low-density lipoprotein (LDL)-cholesterol, high-density lipoprotein (HDL)-cholesterol and triglycerides were assessed locally using the routine procedures of the hospital laboratories. The Framingham cardiovascular index was determined as 10-year risk according to published calculations [14]. The risk score was calculated as the sum of by-gender sub-scores of age, total cholesterol level, HDL-cholesterol level, smoking history and systolic blood pressure determined at each time point. Quality of life was evaluated from the Questions on Life Satisfaction-Hypopituitarism (QLS-H) questionnaire and Z-scores calculated from normative data [15].
Data analysis and statistics
Data were analysed for patients in Italy who were followed in HypoCCS from 1995 to December 2012. Duration of GH treatment for these patients ranged from < 1 to > 16 years. For the present analysis, the patients were divided into three groups based on duration of therapy: group A received GH treatment for ≤ 2 years (n = 451), group B received GH for > 2 to ≤ 6 years (n = 387) and group C received GH for > 6 years (n = 395). The following parameters were evaluated: demographics, GH deficiency diagnosis, BMI, lipid profile, GH dose, IGF-I SDS, Framingham cardiovascular risk and quality of life. Data are shown as mean ± standard deviation or with 95% confidence intervals (CI) for continuous variables, and number of patients (percentage of total patient number) for categorical variables. Baseline variables and changes from baseline to last available visit on GH treatment were compared across treatment duration groups. Differences between the duration of treatment groups were assessed using ANOVA for continuous variables and Chi-squared tests for categorical variables, with P < 0.05 considered statistically significant. All analyses of differences between duration groups were repeated for subgroups based on the onset of GH deficiency (AO and CO), and gender (male and female). The effect of age at last visit was assessed for continuous variables using logistic regression with group C as the reference group, assessing effect of age and its interaction with treatment duration groups. No adjustments for multiplicity were made due to the ad hoc nature of the analysis.
Results
There were no statistically significant differences between the duration-of-treatment groups for mean baseline age, proportion of males, BMI, onset of GH deficiency, lipid profile, IGF-I SDS or quality of life (Table 1). These parameters did not differ significantly when the groups were compared within individual subgroups of AO, CO, male and female patients. Peak GH following GH-releasing hormone (GHRH) + arginine tests did not differ significantly between duration groups overall or for any individual subgroup.
There was a significant difference between the groups in the type of stimulation test used for diagnosis of GH deficiency (Table 2). In group C, with the longest duration of GH treatment, the GHRH + arginine test was used more frequently, and tests using either GHRH or arginine alone and the insulin tolerance test were used less frequently than for the other groups. The difference was significant overall and in AO, but not CO, patients and in male, but not female, patients.
The difference between groups for the cause of GH deficiency, as reported by the investigator, was statistically significant for AO patients, although not for patients overall or for CO patients (Table 3); there was also no significant difference when analysed by gender. For the AO patients, there was a higher proportion with a diagnosis of craniopharyngioma and a lower proportion with idiopathic GH deficiency in group C with the longest treatment duration in the study.
There was no statistical difference between the groups for mean GH dose at start of treatment, except in female patients where mean dose increased with increasing treatment duration (Table 4). Mean GH dose at the last study visit also did not differ significantly between groups, again, except for female patients where those with longest duration had a higher mean dose than those with shortest duration. The mean change in dose from baseline to last visit was significantly different for patients overall and in AO, but not CO, and in male, but not female, patients. The largest decrease in all subgroups was seen in the group with the longest duration of treatment. GH dose at last visit was significantly affected by age (P < 0.001), but the interaction was not significant (P = 0.063) indicating that the age effect was similar in each group.
The increase in mean BMI from baseline to last visit differed significantly by treatment duration, increasing more in patients with the longest duration of treatment (Table 5). BMI at last visit was not significantly affected by age at last visit, either as a direct effect (P = 0.093) or interaction (P = 0.953). The significant difference between the groups for increase in mean BMI was seen overall and in CO patients, but not AO patients or in the by-gender analysis. The increase in mean IGF-I SDS at last visit was greater in group C with the longest duration of treatment. The difference between the groups for IGF-I SDS increase was significant overall and for female patients, but not for the other categories. Age at last visit had an effect on IGF-I SDS at last visit (P = 0.003), while the interaction with group effect was not significant (P = 0.300).
There was a decrease from baseline to last visit in mean total cholesterol and in mean LDL-cholesterol concentrations in group C with the longest duration of treatment; for both concentrations, 95% CI excluded 0, indicating a significant effect, for patients overall and AO and male patients (Table 5). The interaction of age at last visit with treatment duration difference was significant for total cholesterol (P < 0.001) and LDL-cholesterol (P = 0.017) concentrations at last visit, indicating that the effect of age differed between the groups. Changes in triglyceride concentrations were very variable, with wide 95% CI, and showed little effect of GH treatment duration except for CO patients where the longest duration group showed an increase in concentration. There was a significant interaction of age with treatment duration on triglyceride concentrations at last visit (P = 0.019). No significant between-group differences were seen for changes in HDL-cholesterol concentration.
The mean Framingham cardiovascular risk index increased to a greater extent in the groups with longer duration of GH treatment, with no overlap of 95% CI values for group A (shortest duration) and group C (longest duration), for patients overall and AO and male patients. At last study visit (Table 5), there was a significant effect of treatment duration for patients overall and by category of AO and CO GH deficiency and in male patients, though not in female patients. There was no significant effect of age at last visit on change in Framingham cardiovascular risk at last visit (P = 0.593) and interaction of age with GH treatment duration was not significant (P = 0.064).
The QLS-H questionnaire was completed by only a limited number of patients. At baseline, the mean and 95% CI for the quality of life Z-score was below 0 for each group [group A − 1.20 (95% CI − 1.49 to − 0.90); group B −1.07 (95% CI − 1.33 to − 0.81); group C − 1.16 (95% CI − 1.42 to − 0.90)], with no significant difference between the treatment duration groups (P = 0.777). There were insufficient numbers of patients with available data to evaluate changes from baseline.
Discussion
Patients with GH deficiency, whether starting during adulthood or with onset during childhood and continuing in adulthood, require GH treatment throughout life to correct metabolic abnormalities. Our analysis of metabolic parameters in adult patients with GH deficiency in Italy showed effects of duration of GH treatment on IGF-I SDS, BMI, lipids and Framingham cardiovascular risk. The analysis also indicated differences in the GH stimulation tests used and the diagnosed cause of the GH deficiency.
In Italy, the GHRH + arginine test was used for approximately 70% of patients, in contrast to the global data from HypoCCS where the test was used in less than a quarter of the patients [11]. In Italy, a higher proportion of patients in the longest GH treatment duration group received the GHRH + arginine test, whereas a lower proportion of patients received other tests. This could indicate that physicians were more confident about long-term GH replacement for patients diagnosed as GH-deficient using the more sensitive and accurate GHRH + arginine test [16]. This was particularly noticeable for AO patients and was consistent with the less-frequent diagnosis of idiopathic GH deficiency and more-frequent diagnosis of craniopharyngioma in the AO patients in the longest duration of treatment group. However, it may also relate to changes over time in GH stimulation tests and diagnoses that were observed previously for patients entered into HypoCCS between 1996 and 2005 [11].
GH dose for patients overall was not significantly different between treatment duration groups at the start of treatment, but was decreased from baseline to last study visit to a greater extent in the group with the longest treatment duration. In the patients with the longest GH treatment duration, the 95% CI did not include zero, indicating a significant decrease in dose. Because the aim was to assess changes according to duration of GH treatment, the whole cohort including all three groups was not analysed; however, a previous analysis of the patients, on the basis of severity of GH deficiency, indicated that the dose increased over the first 5 years and then fluctuated [12], suggesting that for the whole cohort the dose decrease in the longer duration group was balanced by an increase in the shorter duration group. Mean doses in female patients were higher than in male patients at treatment start and last visit, with no overlap in 95% CI for the two longer duration groups, and in female patients no significant difference was seen between groups for change to last visit. This was consistent with the need for a higher GH dose in female patients and indicated that endocrinologists in Italy involved in HypoCCS were aware of the pathophysiological issue that female patients tend to be more resistant to GH than male patients [17,18,19,20]. Mean doses in patients with CO GH deficiency were higher than in those with AO GH deficiency, consistent with the requirement of a higher dose in patients at a younger age to optimise body proportions [21]. GH dose in overall patients with the longest duration of treatment significantly decreased from baseline to last visit, as indicated by 95% CI values that did not include 0. This reduction in dose could reflect a decreased requirement based on the physiological decrease of IGF-I with age [22, 23]. A significant direct effect of age at last visit was observed for GH dose at last visit, suggesting that the decrease in dose could possibly be more evident in patients with longer term treatment.
IGF-I SDS was increased to a greater extent in patients with longer duration of GH treatment overall, although this was associated more with female and CO patients reflecting their higher GH doses. Decreasing IGF-I with ageing has been shown in some studies to be associated with increased atherosclerosis and cardiovascular disease events [24,25,26], and it was reported that this was related to components of the metabolic syndrome [26]. An increase in BMI in the patients with the longest duration of treatment was observed, with a significant difference between duration groups. This was seen for patients overall, but was particularly apparent in patients with CO GH deficiency. While BMI generally tends to increase with age in the general population [27,28,29], no significant effect of age at last visit or interaction with duration of treatment was found; however, adult GH-deficient patients have a higher BMI at a younger age with no change with increasing age [29] and when treated with GH, an increased BMI was only seen after 7 years or more [9].
Significant decreases in total and LDL-cholesterol concentrations occurred in the group of patients with the longest duration of GH treatment; this may indicate persistent effects of GH treatment on these parameters. The 95% CI values for decreases in both total cholesterol and LDL-cholesterol excluded 0 in the group with the longest duration of GH treatment for patients overall, AO patients and male patients. GH treatment of adult patients has been shown in several studies to decrease total and LDL-cholesterol levels [1, 4, 8, 21]. In contrast to total and LDL-cholesterol, triglyceride concentrations appeared to increase in patients with longest duration of GH treatment; however, this was primarily due to an increase in the patients with CO GH deficiency. The results for triglycerides were in accordance with studies that generally show no effect of GH treatment on triglyceride concentrations [8, 10] and may simply reflect an increase with ageing.
Despite the decreased total and LDL-cholesterol concentrations in the group of patients with longest duration of GH therapy, the Framingham cardiovascular risk index increased in these patients as expected due to the progressive ageing of patients. The significant difference between GH treatment duration groups was seen overall, in patients with AO GH deficiency and in male patients. However, the increase in the Framingham cardiovascular risk index may be the result of the increased age of patients in the longest duration group. Total cholesterol was significantly decreased and HDL-cholesterol was not significantly changed, while LDL-cholesterol was significantly increased but not included in Framingham score calculation. Additionally, systolic blood pressure was not analysed but considered unlikely to change, and the proportion of smokers was similar during the study. Therefore, it is clear that patients’ age at last visit is likely to have had a major impact on Framingham cardiovascular risk without having a significant effect overall. This would suggest that GH, at the dose used, could not control all the factors involved in cardiovascular risk and highlights the importance of continued observation of all factors associated with cardiovascular risk during long-term GH replacement in adult patients.
The strength of this study lies in providing data on GH therapy according to duration of follow-up that has been obtained from daily clinical practice.
In conclusion, in a real-life setting such as the Italian HypoCCS study, increased IGF-I SDS, decreased LDL-cholesterol, more robust diagnostic tests and more severe causes of hypopituitarism (i.e. craniopharyngioma) are associated with a longer term duration of GH therapy. Thus, the presence of such surrogate markers that help to give confidence in a diagnosis of GH deficiency predicts a longer duration of treatment.
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Acknowledgements
HypoCCS was sponsored by Eli Lilly and Company. The authors thank all the investigators who participated in the study and all the patients. Medical writing assistance was provided by Peter Bates (Cambridge Medical Writing Services, UK) and editorial support by Caroline Spencer (Rx Communications, UK), funded by Eli Lilly and Company.
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This study was funded by Eli Lilly and Company.
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Vincenzo Rochira, Salvatore Cannavo, Paolo Beck-Peccoz, Gianluca Aimaretti, Maria R Ambrosio, Carolina Di Somma, Diego Ferone, Carla Lubrano, Carla Scaroni, Antonella Giampietro, Salvatore M. Corsello and Maurizio Poggi declare that they have no conflicts of interest. Gilberto Mossetto and Nan Jia are employees of Eli Lilly and Company. Marco Losa has received consulting fees from Eli Lilly, Ipsen, and Pfizer.
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All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.
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Informed consent was obtained from all individual participants included in the study.
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The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.
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Rochira, V., Mossetto, G., Jia, N. et al. Analysis of characteristics and outcomes by growth hormone treatment duration in adult patients in the Italian cohort of the Hypopituitary Control and Complications Study (HypoCCS). J Endocrinol Invest 41, 1259–1266 (2018). https://doi.org/10.1007/s40618-018-0860-x
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DOI: https://doi.org/10.1007/s40618-018-0860-x