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CLINICAL STUDY |
Department of Endocrinology, University Hospital, Antwerp, Belgium, 1 University Hospital, Copenhagen, Denmark, 2 KIGS/KIMS/ACROSTUDY Medical Outcomes, Pfizer Endocrine Care, Sollentuna, Sweden, 3 St Bartholomew’s Hospital, London, UK, 4 Sahlgrenska University Hospital, Göteborg, Sweden, 5 National Medical Center Budapest, Hungary and 6 Department of Pharmacy, Uppsala University, Uppsala, Sweden
(Correspondence should be addressed to R Abs; Email: roger.abs{at}uza.be)
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Abstract |
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 Top Abstract IntroductionPatients and methodsResultsDiscussionReferences |
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Design: Data for analysis were retrieved from KIMS (Pfizer International Metabolic Database). Serum concentrations of total cholesterol, high-density lipoprotein (HDL)-cholesterol, low-density lipoprotein (LDL)-cholesterol and triglycerides were obtained from 2589 patients at baseline and from 1206 patients after 1 and 2 years of GH replacement therapy. Body mass index (BMI), waist and hip, resting blood pressure and body composition were also measured.
Results: At baseline, the unfavourable effects of GHD were most obvious in the lipid profile demonstrating elevated mean total and LDL-cholesterol, in the increased waist circumference and the elevated BMI. The cholesterol concentration, BMI and body composition were significantly adversely affected by a number of factors, including age, sex and the use of anti-epileptic drugs. The therapeutic effect of GH was essentially uniform across the whole population. GH replacement reduced significantly the mean total and LDL-cholesterol, the waist circumference and the fat mass and was maintained during 2 years.
Conclusions: This analysis of a large number of patients confirmed that GHD adults present with an increased cardiovascular risk. The sustained improvement of the adverse lipid profile and body composition suggests that GH replacement therapy may reduce the risk of cardiovascular disease and the premature mortality seen in hypopituitary patients with untreated GHD.
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Introduction |
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TopAbstractIntroductionPatients and methodsResultsDiscussionReferences |
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The hypothesis that GHD increases the risk of cardiovascular disease is supported by findings that adult patients with GHD present a series of risk factors, such as adverse lipid profiles (10–12), increased blood pressure, abnormal body composition (13, 14), increased body weight (15, 16), increased coagulability (17), and increased markers of inflammation (18). These multiple abnormalities promote the development of an accelerated atherosclerotic disease, as shown by decreased aortic compliance (19) and increased intima-media thickness (20).
There is increasing evidence that GH replacement provides protection against the development of myocardial infarction and could thus impact on the increased mortality rate (5). The well-known favourable changes induced by GH on the different cardiovascular risk factors may explain this recent finding. The effect on body composition has been demonstrated by different techniques (21–24). GH also has a major impact on lipid metabolism (23–27). Markers of inflammation are positively influenced by GH replacement (28). As a result of GH replacement, the abnormal aortic compliance and intima-media thickness normalise (29, 30).
The above-mentioned studies were usually conducted on small groups of patients and over a period of short time. Furthermore, not all studies have revealed the same abnormalities before and the same changes after GH treatment (28). Recently, a meta-analysis based on these studies was published, confirming a beneficial effect, yet in total not in very large numbers of patients (31). The aim of the present analysis was to further elucidate our understanding of the association between GHD and dyslipidaemia as well as other cardiovascular risk factors, and to determine the effect of long-term GH replacement therapy in a large number of patients. Secondarily, we set out to determine whether the cardiovascular risk factors in these patients were influenced by variables such as age, sex and the age of onset of GHD. The patient data in this analysis were retrieved from KIMS (Pfizer International Metabolic Database), the largest database for monitoring the efficacy and safety of long-term GH replacement in GHD adults.
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Patients and methods |
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TopAbstractIntroductionPatients and methodsResultsDiscussionReferences |
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Patients from KIMS were included in the analysis if they satisfied the following conditions: they had severe GHD indicated by a GH peak response <3 µg/l after provocative testing by insulin, arginine or glucagon; they had received no GH therapy at any time before entering KIMS (naive patients, 80%) or had received no GH therapy for at least 6 months prior to entry (semi-naive patients, 20%).
In total, 2589 patients (mean age, 44.2±14.6 years) were included in the analysis. Females numbered 1263 (48.8%; mean age 43.6±14.2 years), of which 769 were pre-menopausal or oestrogen-supplemented (29.7%; mean age, 39.5±12.5 years) and 494 post-menopausal or notoestrogen-supplemented (19.1%; mean age, 50.1±14.4 years) and males numbered 1326 (51.2%; mean age, 44.8±15.0 years). Adult-onset patients accounted for 77.5% and childhood onset for 22.5%.
IGF-I measurements
Until November 2002, serum insulin-like growth factor I (IGF-I) was determined by radioimmunoassay after acid-ethanol precipitation of the binding proteins (Nichols Institute Diagnostics, San Juan Capistrano, CA, USA). Then a chemiluminescence immunoassay (Nichols Advantage® System) was introduced (32). Long-term reproducibility, measured during a time period of >1 year, showed a CV <9% in the concentration range of 130–850 µg/l. The assay detection limit was 30 µg/l. All measurements were performed in a central laboratory.
Lipid measurements
Serum concentrations of total cholesterol (33), high-density lipoprotein (HDL)-cholesterol (34) and triglycer-ides (35) were measured directly and expressed as mmol/l. All measurements of lipid variables were performed in the same central laboratory. Serum concentrations of low-density lipoprotein (LDL)-cholesterol were estimated using Friedewald’s formula (36). Due to low accuracy, the formula was not applied when the level of triglycerides exceeded 4.5 mmol/l. The conversion factors are: 1 mmol/l=38.5 mg/dl for cholesterol and 1 mmol/l= 90.9 mg/dl for triglycerides. The ratio of total cholesterol over HDL-cholesterol was calculated.
Profile of lipids
Mean baseline concentrations of all four lipid fractions were calculated for all 2589 patients collectively. Mean baseline lipid concentrations were also calculated for patients categorised according to age: <20 (n=122), 20–29 (n=382), 30–39 (n=479), 40–49 (n=590), 50–59 (n=595), >60 years (n=421) and according to gender: males (n=1326), pre-menopausal females (n=769), or post-menopausal females (n=494).
The percentage of patients with baseline lipid concentrations exceeding the desired target values was calculated for: total cholesterol >5.20 mmol/l (200 mg/dl); HDL-cholesterol <1.04 mmol/l (40 mg/dl) in males and <1.30 mmol/l (50 mg/dl) in females; LDL-cholesterol >3.38 mmol/l (130 mg/dl); and for triglycerides >1.65 mmol/l (150 mg/dl) (37).
Mean baseline concentrations of total cholesterol were calculated for patients categorised according to: the time of onset (childhood- vs adulthood-onset of the disease), the estimated duration of GHD, the severity of hypopituitarism expressed as the number of pituitary hormone deficiencies present in addition to GHD, the severity of GHD expressed as the standard deviation score (SDS) for the serum IGF-I concentration, the aetiology of GHD (non-functioning pituitary adenoma, craniopharyngioma, idiopathic, prolactinoma, Cushing’s disease, acromegaly, and other aetiologies), previous radiotherapy or not, body mass index (BMI), waist/hip ratio (WHR), waist circumference, smoking/non-smoking, use of anti-epileptic drugs and lipid-lowering drugs and diabetes mellitus.
To evaluate the effect of GH replacement, mean lipid concentrations were calculated for the 1st year and 2nd year time-points in 1206 patients and compared with their baseline concentrations. The percentage of patients with lipid concentrations exceeding the desired target values during GH replacement at these two time points was compared to the data prior to therapy.
Profile of other cardiovascular risk factors
Resting blood pressure (mmHg), BMI (kg/m2), WHR and waist circumference (cm) were measured both for the group of patients contributing with baseline data only (n=2589) and for the subgroup of patients contributing with data at both baseline and after 1 and 2 years of GH treatment (n=1206). The percentage of patients with a blood pressure above the target value of 130/85 mmHg and with a waist circumference above 102 cm in men and above 88 cm in women was also calculated (37). Body composition was measured at baseline in two different groups of patients by dual-energy X-ray absorptiometry (DXA) or by bio-impedance analysis (BIA) with assessment of estimated values for lean and fat. In a subgroup of patients, both measurements were repeated after 1 and 2 years of GH replacement. Both DXA and BIA measurements were performed by a variety of different methods from each individual’s participating centre without any attempts to obtain uniform calibration. The baseline data were categorised according to the same factors as mentioned for total cholesterol, although numbers in each individual group were not identical to those for cholesterol, due to missing values. The numbers are mentioned in Results section and also in Tables 1
–4.
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To study the influence on blood lipid levels by baseline characteristics, multiple regression analyses were performed. Outcome lipid variables such as cholesterol were treated as continuous variables. Data, which were not normally distributed were subjected to logarithmic transformation. Potentially influencing factors, such as age, sex, waist, diagnosis of GHD etc., were categorised (see above) or treated as a continuous variable if suitable. Heterogeneity tests were performed with F-tests. Trend tests were performed with Wald tests. Linear trend tests confer to linear compartment of trend. All tests were adjusted for age at baseline and/or gender.
Longitudinal analyses were performed with repeated measurements regression. The within-patient dependency of the data was modelled by assuming unstructured variance-covariance matrixes. Comparisons of mean values at the 1st and 2nd year visits, versus baseline values, were performed assuming identity link and a normal distribution. Tests were performed with F-tests or Wald tests. For analyses of the proportion of patients outside a target, a logit link and a binomial distribution were used.
In the analyses of the change in cholesterol over time by baseline cholesterol category, adjustment for effects of regression to the mean was done according to the methods described by Johnson and George (38). Analyses were performed using SAS software version 8.02. Multiple regressions were run with PROC GLM. PROC MIXED and PROC GENMOD were used for repeated measurement regression.
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Results |
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TopAbstractIntroductionPatients and methodsResultsDiscussionReferences |
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Total cholesterol.
The observed overall mean total cholesterol concentration±S.D. was 5.9±1.3 mmol/l (Table 1
). The mean increased across age categories more or less linearly, from 5.0 mmol/l in the <20 age category up to 6.1 mmol/l in the 40 – 49 age category, thereafter no further increase was observed (P for linear age-trend <0.0001; Fig. 1). Females showed a 0.2 mmol/l higher mean value than males (95% confidence interval (CI): 0.1–0.3; P<0.0001). There was no statistically significant difference between pre-menopausal and post-menopausal women.
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HDL-cholesterol.
The overall mean±S.D. was 1.2± 0.4 mmol/l (Table 1) and remained relatively constant over age (P for heterogeneity =0.14; P for trend = 0.92). Females showed a 0.2 mmol/l higher mean value than males (95% CI: 0.2–0.3; P<0.0001). Post-menopausal women had a slightly lower mean compared to pre-menopausal women (0.1 mmol/l, P<0.05).
Approximately 49% of patients (95% CI: 47–51%) were below the desired target value; 46% males, 49% pre-menopausal females and 57% post-menopausal females.
Total cholesterol/HDL-cholesterol ratio. Due to the skewed distribution for this variable, the geometric mean was calculated, which was 4.8 (10th–90th percentile: 3.1–7.4). Similar to the mean of total cholesterol, this geometric mean increased by age in a linear fashion: from 4.1 in the <20 age category up to 5.0 in the 40–49 age category, after which it levelled off to 4.8 in patients of 60+years (P for linear age-trend <0.0001). Females showed a significantly lower geometric mean compared to males: –14.1% (95% CI: –16.3% – –12.0%; P<0.0001). For the 40–49 age category, this percentage of –14.1% translates to an absolute difference of 0.77.
Approximately 59% of the patients (95% CI: 57%–61%) were above the desired target value of 4.5. For males, the corresponding figure was 69%, pre-menopausal females 44%, and post-menopausal females 55% (P for heterogeneity <0.05). The increase in percentage above target by age category was quite steady but levelled off successively: <20 year, 37%; 20–29 year, 49%; 30–39 year, 58%; 40–49 year, 62%; 50–59 year, 66% and 60+year, 63% (P for linear trend <0.0001).
LDL-cholesterol.
The overall mean±S.D. was 3.7± 1.1 mmol/l, following the same pattern as for total cholesterol (Table 1).
Triglycerides.
The geometric mean for the overall cohort was 1.8 mmol/l (10th–90th percentile: 0.9–3.8; Table 1). The linear increase by age was significant (P<0.0001) but levelled off in a similar fashion to the other lipid variables.
Approximately 57% of males, 49% of pre-menopausal females and 60% of post-menopausal females had higher values than the target.
Multiple regression models for baseline lipids with adjustment for age and gender
Total cholesterol. Of the variables examined besides age and gender, the onset of GHD, duration of GHD, severity of hypopituitarism, severity of GHD, aetiology, radiotherapy, BMI, WHR and waist circumference did not statistically significantly influence the baseline cholesterol concentration. The following variables were found to have an effect:
There was no significant association between baseline total cholesterol level and IGF-I SDS (P for linear trend =0.19; P for heterogeneity =0.68). LDL-cholesterol showed similar trends as that of total cholesterol.
HDL-cholesterol. Three variables showed a statistically significant, decreasing linear trend for HDL-cholesterol concentrations. As the HDL-cholesterol concentrations were independent of age, the presented mean values are applicable for all ages.
Other variables associated with a significantly lower mean HDL-cholesterol concentration (–0.1 mmol/l) were smoking, lipid-lowering drugs and diabetes mellitus (P<0.01).
Triglycerides
Patients with craniopharyngioma showed 50% higher geometric mean triglycerides compared to patients with idiopathic GHD (95% CI: 37%–65%; P<0.0001). The other aetiological groups showed between 16 and 23% higher values than idiopathic GHD (<0.0001<P<0.03). Patients with childhood onset of the disease had 8% lower values, smokers 10% higher values, patients taking lipid-lowering drugs 23% higher values; patients taking anti-epileptic drugs 13% higher values, and diabetic patients 24% higher values (P<0.02 in all cases).
BMI, WHR, blood pressure and body composition at baseline
Baseline data regarding BMI, WHR, waist circumference, blood pressure and body composition are given in Table 1.
Obesity was prominent, as 806 of 2527 patients (32%) had a BMI >30 kg/m2, while 98 patients (4%) had a BMI <20 kg/m2. BMI increased with age, WHR and waist circumference (data not shown). It was higher in post-menopausal females than in males, in adult-onset GHD than in childhood-onset GHD, in patients with craniopharyngioma than in patients with other aetiology, in patients who had cranial irradiation, in patients with multiple pituitary deficiencies, in smokers, in patients with diabetes mellitus, and in patients taking anti-epileptic or lipid-lowering drugs. Fat mass measured by BIA or DXA demonstrated largely similar associations (data not shown).
Waist circumference was above the target value in 46% of patients, 40% of males, 56% of females, 51% of pre-menopausal females, and 64% of post-menopausal females. Fifteen percent of patients had a medical history of hypertension. Blood pressure was above the target value in 26% of patients, 28% of men, 23% of females, 20% of pre-menopausal females, and 28% of post-menopausal females. Blood pressure correlated with age, severity of GHD, WHR, waist, and smoking, while systolic blood pressure correlated additionally with lipid-lowering drugs and presence of diabetes mellitus (data not shown). BMI, waist circumference and blood pressure showed a significantly positive correlation to IGF-I SDS.
Change in lipid profile during GH replacement
Total cholesterol.
Statistically significant reductions in total cholesterol were observed after both 1 year and 2 years of GH replacement therapy: –0.4 mmol/l (95% CI: –0.4––0.3; P<0.0001) and –0.5 mmol/l (95% CI: –0.5––0.4; P<0.0001), respectively (Table 2). The additive effect during the second year of treatment was small, –0.1 mmol/l, but still significant compared to the first year (95% CI –0.15––0.04; P=0.001). Moreover, assuming a constant proportional change, the higher the baseline value, the larger the absolute decrease in cholesterol, even after adjustment for regression to the mean: 
(mmol/l)/(mmol/l at baseline) = –0.06 (P=0.01). This relationship would predict that a patient with a hypothetical baseline value of 7.5 mmol/l would demonstrate a change in cholesterol of 7.5x(– 0.06)=–0.45 mmol/l after 1 year of treatment. After 2 years of treatment, these observations were strengthened in all subgroups (P<0.0001). The proportional effect per mmol/l at baseline was increased to –0.11 (P=0.0006).
The change in total cholesterol concentration during GH replacement therapy was essentially unaffected by any of the other variables examined. GH replacement also induced a decrease in total cholesterol in patients taking lipid-lowering drugs. In all categories, total cholesterol concentration was significantly reduced after both 1 and 2 years.
A highly significant decrease in the percentage of patients with values exceeding target value was observed after both 1 and 2 years of treatment (Table 3).
Descriptive model for change in total cholesterol by age and gender.
A descriptive model for mean total cholesterol by age, gender and visit (baseline, 1 year, 2 years) was also fitted. This model indicates that improvement in total cholesterol concentrations was largest during the first year of treatment and was greater, the older the patients were at the start of the treatment. During the second year of treatment, the improvement was smaller and indeed absent in younger ages. Females had in average, 0.3 mmol/l higher mean cholesterol values than males (95% CI: 0.2–0.4). Otherwise, males and females showed the same pattern of change (Fig. 2).
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50. The corresponding standard error estimate for each parameter was (0.045) –(0.059) –(0.047) –(0.023) – (0.0069) – (0.00033) – (0.00065) – (0.0010), respectively. The interaction test between gender and visit (GV) was not significant (P=0.22) and the term was not included in the model. The model was fitted assuming the same age pattern for both genders.
Other lipid parameters.
Mean HDL-cholesterol changed from 1.3 mmol/l to 1.2 mmol/l after 2 years of treatment (Table 2). Although this change was minimal, it was statistically significant. The percentage of patients with a value above target increased significantly (Table 3).
The geometric mean of total cholesterol over HDL-cholesterol ratio decreased significantly over the 2-year treatment period from 4.8 to 4.5 (P<0.0001). The decrease was significant in both males and females (Table 2). The percentage of patients with a ratio exceeding the target value also decreased significantly during the treatment period (Table 3).
The major change in total mean cholesterol is accounted for by the change in mean LDL-cholesterol, which was –0.3 mmol/l after 1 year and –0.4 mmol/l after 2 years (Table 2). A highly significant decrease in the percentage of patients with values exceeding the target was observed after both 1 and 2 years of treatment (Table 3).
No statistically significant changes in geometric mean triglycerides were observed after 1 and 2 years of GH therapy, respectively (Table 2 and Table 3).
Changes in BMI, blood pressure, WHR and body composition during GH replacement
GH replacement therapy did not induce significant changes in BMI or blood pressure after 1 and 2 years of GH treatment (Table 4).
There was a significant reduction in WHR, waist circumference, and fat tissue both by DXA and BIA with a corresponding increase in lean body mass (also both by DXA and BIA) (Table 4). The changes were related with a significant trend to aetiology of pituitary diagnosis, year of GHD and BMI, but not to any of the other tested co-variables (data not shown).
There was a significant decrease in the percentage of patients with blood pressure and waist circumference exceeding the target value during the treatment period (Table 3).
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Discussion |
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TopAbstractIntroductionPatients and methodsResultsDiscussionReferences |
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The lipid data are in agreement with previous observations showing that GHD adults have an adverse lipid profile; (12, 25, 26, 31, 39, 40). The dyslipidaemia seen at baseline in this analysis was characterised by increased concentrations of total cholesterol and LDL-cholesterol and normal concentrations of HDL-cholesterol and triglycerides. An identical pattern has been observed before in adults with GHD (26), while other researchers have reported decreased concentration of HDL-cholesterol and increased concentration of triglycerides (25, 39).
Our investigation on the effects of a range of potentially influential variables on the baseline lipid profile suggests that hypercholesterolaemia is most marked in elderly patients, women, smokers and patients taking anti-epileptic medication. The effects observed for age and smoking are not surprising, as these variables are known to increase the risk of hypercholesterolaemia in the general population. The increased baseline concentration of total cholesterol in patients with epilepsy is probably linked to their anti-epileptic medication (41). Our finding that cholesterol concentrations tend to be higher in GHD women than in GHD men is consistent with previous data showing that the risk of premature death from cardiovascular disease is elevated to a greater degree in women with conventionally treated hypopituitarism than in men with this condition (1, 3). However, the details of our findings for men and women contrast with results reported before, showing that the main lipid abnormality in women was a decreased concentration of HDL-cholesterol (12, 42). In the present study, the main abnormality in women was an increase in total cholesterol. Our observation that patients with adult-onset GHD had a concentration of total cholesterol comparable to those with childhood-onset GHD is consistent with the data described before, showing that patients with these conditions differ in many respects but not in cholesterol metabolism (43).
The present analysis has confirmed the adverse profile of both blood pressure and body composition in GHD patients at baseline. Thus 26% of GHD patients, including 15% on anti-hypertensive drugs, had a blood pressure above the target value of 135/85 in keeping with a previous demonstration of GHD patients having a changed circadian blood pressure pattern with more than 30% non-dippers (44).
BMI was adversely affected by adult onset of the disease, anti-epileptic drugs, previous radiotherapy, other hormone deficiencies and it was further increasing with age, blood pressure and cholesterol. Interestingly, BMI correlated positively to IGF-I SDS, and therefore did not seem related to severity of the GHD per se, but rather to the nutritional state. The same pattern was seen for the blood pressure and waist circumference. Such correlations have not been demonstrated previously, possibly because it requires very large patient groups as in the KIMS population. Indirect evidence, however, comes from investigations of the acute effect of the growth hormone receptor antagonist pegvisomant on cardiovascular risk factors in healthy persons (45). They suggested that the secondary metabolic changes, e.g. abdominal fat or inflammatory factors that develop as a result of longstanding GHD, are of primary importance in the pathogenesis of atherosclerosis in patients with GHD.
In this analysis, GH replacement therapy reduced the concentrations of total and LDL-cholesterol, but had no significant effect on the concentrations of HDL-cholesterol or triglycerides. This finding is consistent with results reported previously (25, 31, 40, 46–49), but not all are possibly related to a selection of patients with near-normal baseline values (28). The beneficial effects of GH therapy were essentially homogeneous among the different subgroups studied. In other words, they were largely unaffected by variables such as age, sex or the age of onset of GHD. This contrasts with a number of previous findings suggesting that GH replacement has different effects in different subgroups, such as age of onset (43) or gender (50). The homogeneity of therapeutic effects of GH has been shown before for elderly patients (51) and the additive effect of GH, apart from lipid-lowering drugs has also been demonstrated (52). There was a clear trend of the effects of GH treatment to be greater after 2 years than after 1 year and be most marked in patients with the most pronounced hypercholesterolaemia at baseline.
Vahl et al. have previously shown that the cholesterol-lowering effect of GH is not determined by the concomitant decrease in adiposity, supporting a direct effect of GH on lipoprotein metabolism (40). In support of this, Hana et al. found an increase in lean and a decrease in fat mass in 17 patients with GHD treated over 1 year, without a concomitant change in adipokines and insulin resistance (53). Opposite to this, a randomised, double-blind, placebo-controlled multicentre study of 166 patients with GHD treated over 1 year also found a decrease in fat and increase in lean body mass, but in this case with a concomitant reduction in total and LDL-cholesterol (54). Also recently, Abrahamsen et al. demonstrated that the effects of GH replacement on both lipids and body composition were dependent on dose as well as on the obtained IGF-I level (55). Although we did not find any significant reduction in BMI or blood pressure, GH replacement resulted in a beneficial mean reduction of 2.2 kg of fat and mean increase of 2.2 kg of lean body mass as well as a small reduction in waist circumference.
The discrepancy between results from BMI and other measures of body composition indicates that BMI is a poor predictor in following the effect of GH therapy compared to waist circumference, BIA and DXA, since a shift from fat to lean body mass will not be reflected in BMI if the total body weight is sustained (56). A favourable effect of GH replacement on diastolic blood pressure has been demonstrated by Sverrisdottir et al. in a small series of ten GHD patients treated for 1 year (57). A more careful evaluation of blood pressure was done in 22 patients with measurement of 24-hour ambulatory blood pressure (58). Interestingly, they found a preserved circadian rhythm after 12 months of GH replacement.
The present findings are consistent with previous results showing that GH replacement can improve dyslipidaemia and other cardiovascular risk factors, and that the effect on both body composition and lipids is sustained over years (49, 54, 59, 60). Quantitatively, a recently published meta-analysis of blinded, randomised, placebo-controlled trials on cardiovascular risk factors in GHD adults found that GH treatment significantly reduced LDL-cholesterol by –0.5 mmol/l (vs –0.4 mmol/l after 2 years in the present study), total cholesterol by –0.3 mmol/l (vs –0.4 mmol/l), fat mass by –3.1 kg (vs –2.2 kg), and diastolic blood pressure by –1.8 mmHg (vs –0.6 mmHg), and significantly increased lean body mass by 2.7 kg (vs 2.2 kg after 2 years in present study) (31). The meta-analysis and the data from the KIMS database are thus very similar despite differences in methodology.
Taken together, the results suggest that GH replacement therapy may be important in adults with GHD not only to improve the general health and well-being but also to reduce the risk of premature mortality. This has also been indicated very recently by a demonstration of a 1.3 relative risk reduction according to the Framingham equation by 12 months of GH replacement in GHD adults (non-smokers, without diabetes mellitus, hypertension or vascular disease) (61). However, the recorded individual changes in the cardiovascular risk factors in all the studies are small. So, the global benefit of GH replacement on cardiovascular mortality remains to be determined in larger trials with appropriate end points.
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Acknowledgements |
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TopAbstractIntroductionPatients and methodsResultsDiscussionReferences |
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