AU759025B2 - Use of growth hormone - Google Patents

Description

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AUSTRALIA

PATENTS ACT 1990 DIVISIONAL APPLICATION NAME OF APPLICANT(S): Pharmacia Upjohn AB ADDRESS FOR SERVICE: DAVIES COLLISON CAVE Patent Attorneys 1 Little Collins Street Melbourne, 3000.

INVENTION TITLE: "Use of Growth Hormone" The following statement is a full description of this invention, including the best method of performing it known to us: Q:\OpER\JMS\2350440-div.294.doc 20/10/00 USE OF GROWTH HORMONE The present invention relates to the use of growth hormone, preferably human growth hormone or analogues thereof for the manufacturing of a medicament for treatment of individuals with the Metabolic syndrome (also labeled Syndrome X).

They include individuals with abdominal/visceral obesity and its metabolic and circulatory consequences including insulin resistance, lipoprotein aberrations and hypertension. The medicament is also used to increase insulin sensitivity and for to treatment and prevention of non-insulin dependent diabetes mellitus.

Introduction Striking similarities exhibits between The Metabolic Syndrome 1, 2 (also labeled Syndrome X or Primary Insulin Resistance Syndrome) and untreated GH deficiency in adults 3. The most central findings in both these syndromes are abdominal/visceral obesity and insulin resistance 1, 4-6. Other features common to both conditions are high triglyceride and low high-density lipoprotein cholesterol concentrations, an increased prevalence of hypertension, elevated levels of plasma fibrinogen and plasminogen activator inhibitor-1 activity, premature atherosclerosis and increased mortality from cardiovascular diseases I 4, 7-11 The Metabolic Syndrome is associated with multiple endocrine abnormalities.

They include increased cortisol secretion, blunted secretion of gonadotrophins and sex steroids and abnormalities in the GH/insulin-like growth factor-I (IGF-I) axis 12-14. With increased adiposity GH secretion is blunted with decreased mass of GH secreted per burst but without any major impact on GH secretory burst frequency 15. The serum IGF-I concentration is principally GH dependent and influences GH secretion though a negative feed-back system 16. The serum levels of IGF-I are inversely related to the percentage body fat 15. In addition, we have previously shown that the low serum IGF-I concentration in obesity is predominantly related to the amount of visceral adipose tissue and not to the amount of subcutaneous fat mass 13. These findings, together with other endocrine disturbances in central obesity, suggest that the low GH secretion which i. is observed is secondary to a central disturbance of the neuroendocrine regulation, 10 including the GH/IGF-I axis.

The abdominal/visceral obesity and insulin resistance observed in The Metabolic Syndrome constitute the base for hypertension, dyslipoproteinemia and noninsulin dependent diabetes mellitus.

Replacement therapy with recombinant human GH (rhGH) has demonstrated 15 favorable effects on most of the features of GH deficiency in adults 17. Whether rhGH treatment can improve the metabolic abnormalities observed in abdominal/visceral obesity has never been investigated. In the present study a randomized, double-blind, placebo-controlled design was used to evaluate the effects of rhGH administration in patients with abdominal/visceral obesity In the present study thirty men, 48 to 66 years of age with abdominal/visceral obesity were treated with recombinant human GH (rhGH) in a 9-month randomized, double-blind, placebo-controlled trial. Body fat was assessed from total body potassium and abdominal subcutaneous and visceral adipose tissue was measured using computed tomography. Glucose disposal rate (GDR) was measured during euglycemic, hyperinsulinemic glucose clamp.

In response to the rhGH treatment, total body fat, abdominal subcutaneous and visceral adipose tissue decreased. The GDR (glucose disposal rate) increased in the rhGH-treated group as compared with the placebo-treated one. The mean serum concentrations of total cholesterol and triglyceride decreased while blood glucose and serum insulin concentrations were unaffected by the rhGH treatment.

Furthermore, diastolic blood pressure decreased and systolic blood pressure was unchanged in response to rhGH treatment.

The present study has demonstrated that GH can favorably affect some of the multiple perturbations associated with The Metabolic Syndrome. This includes a reduction in abdominal/visceral obesity an improved insulin sensitivity and favorable effects on lipoprotein metabolism and diastolic blood pressure. Thus, the prevention and treatment of non-insulin dependent diabetes mellitus may be possible.

The findings must be regarded as unexpected and surprising and of utmost 15 interest giving a possibility to treat and prevent diseases associated with increased cardiovascular morbidity and mortality.

INVENTION

The invention relates to the use of growth hormone, preferably human growth hormone or analogues thereof for the manufacturing of a medicament for treatment of non-insulin dependent individuals with the Metabolic syndrome (also labeled Syndrome X) and insulin resistance as claimed in the claims on file.

By analog is meant a substance having the same biological activity as described here and having at least 65 homology with natural occurring growth hormone.

Legends to figures.

Figure 1. Mean total body fat calculated from total body potassium, abdominal subcutaneous adipose tissue (AT) area at the level of L4-L5 and volume of visceral

AT.

Figure 2. Abdominal subcutaneous and visceral adipose tissue determined with computed tomography at the level of L4-5 in one man before and after 9 months of rhGH treatment Figure 3. Mean fasting blood glucose, serum insulin and glucose disappearance rate (GDR).

10 EXAMPLE Subjects and methods Patients Thirty men (48 to 66 years of age) were studied (Table They were recruited by advertisement in a local newspaper. The criteria for inclusion in the study were 15 age approximately 50 to 65 years with a body mass index between 25 and kg/m 2 an IGF-I less that 160 pg/L (low normal) 18 and a waist hip ratio of more that 0.95. The criteria for exclusion were overt diabetes mellitus, previous cardiovascular event or heart disease.

In the rhGH treated group, two patients were receiving treatment for hypertension with both atenolol (100 mg per day) and nifedipin (40 mg per day) and one patient had slight asthma, treated with salmeterol and terbutalin inhalations. In the placebo treated group, one patient had a slight depressive disorder and was receiving paroxetin (10 mg per day). These medications were kept stable during the study period.

Study design This study was a 9 month randomized, double-blind, placebo-controlled trial of the administration of rhGH. Informed consent was obtained from each patient before the study. The study was approved by the Ethics Committee at the University of Goteborg and by the Swedish Medical Products Agency, Uppsala, Sweden.

Treatment The daily rhGH dose was 9.5 ug/kg (0.20 IU/kg body weight/week), administrated subcutaneously before bedtime. The dose was reduced by half in 10 the event of side-effects. The average dose reduction during the 9-month study was 0.17 mg per day (range -1.7 to The placebo vials contained the same vehicle as the rhGH vials and both preparations were visually indistinguishable.

Compliance assessed by counting the returned empty vials and expressing that number as a percentage of vials needed for the treatment period was 87.3 (range s 32-100).

Study protocol The patients were studied as out-patients before and after 6 weeks, 6 and 9 months of treatment. Physical and laboratory examinations were performed at all visits.

The euglycemic hyperinsulinemic clamp, adipose tissue needle aspiration and measurement of blood pressure and heart rate were performed at baseline, 6 weeks ai~d after 9 months of treatment. Body weight was measured in the morning to the nearest 0.1 kg wearing indoor clothing, and body height was measured barefoot to the nearest 0.01 m. The body mass index was calculated as body weight in kilograms divided by height in meters squared. Waist circumference was measured in the standing position with a flexible plastic tape midway between the lower rib margin and the iliac crest, and the hip girth at the widest part of the hip.

Systolic and diastolic blood pressure were measured after 5 minutes of supine rest using the sphygmanometric cuff method. This measurement was repeated after one minute and the mean value was used.

Total-body potassium was measured by counting the emission of 1.46 MeV gamma-radiation from the naturally occurring 4 0 K isotope in a high-sensitive 3n whole body counter with a coefficient of variation (CV) of Fat-free mass (FFM) was estimated by assuming a potassium content of 64.7 mmol/kg FFM 19 and body fat (BF) was calculated as body weight-FFM. A five-scan computed tomography technique was used (Philips Tomoscan 350) to measure abdominal S 10 adipose tissue. The five levels were derived from two scanograms and included one scan at the level of the mid-thigh with the lower edge of symphysis as a reference point. The other four levels were the lower edge of symphysis, lumbar disc, L3-4 lumbar disc and a scan at the level of liver and spleen. The tissue areas and anatomic boundaries were determined as described previously 20. Total volume of visceral adipose tissue was determined from the five-scan model.

Sagittal diameter and abdominal subcutaneous and visceral adipose tissue areas were determined at the level of *0 *0: A euglycemic, hyperinsulinaemic glucose clamp was performed after an overnight fast as previously described 14. In brief, insulin was infused together with glucose into a venous catheter with the tip at the level of the axillary vein at appropriate rates to obtain submaximal insulin concentrations. Blood glucose concentrations were monitored every 10 min. and glucose infusion rate was adjusted to fasting levels. Glucose disappearance rate (GDR) was measured for 20 minutes in steadystate conditions, which was reached after 100 min. The insulin concentrations during steady state were 214 10 pIU/mL before treatment, 226 12 gIU/mL at 6 weeks and 213 11 lIU/mL at 9 months. During the clamp, in steady-state conditions, a subcutaneous abdominal adipose tissue biopsy was obtained by needle aspiration for the determination of lipoprotein lipase (LPL) activity. The needle aspiration was performed under local anesthesia, 0.1 m lateral to the umbilicus. The biopsies were immediately frozen in liquid nitrogen and stored at until assay.

Analytic methods Total LPL activity in adipose tissue was determined after homogenization of the tissue in the detergent-containing buffer as described previously 21. Bovine skim milk was used as a standard to correct for interassay variation. The amount of triglycerides (TG) in the tissue was measured after extraction 22 and weighed after 10 evaporation of solvents. Activity was expressed in milliunits (lmU=l mmol FFA released per min.) per gram adipose tissue and per gram TG. Control experiments showed that the assay was linear with the amount of sample and incubation time over the range used. The within-assay CV was 4.3%.

Blood samples were drawn in the morning after an overnight fast. The serum ooo' 15 concentration of insulin-like growth factor-I (IGF-I) was determined by a hydrochloric acid-ethanol extraction radioimmunoassay using authentic IGF-I for labeling (Nichols Institute Diagnostics, San Juan Capistrano, CA, USA) with within-assay CV of 2.5% and 4.2% at serum concentrations of 125pg/L and 345pg/L respectively. The standard deviation score for IGF-I was then calculated from predicted IGF-I values adjusted for age and sex obtained from the normal population 18 The insulin-like growth factor binding protein-3 (IGFBP-3) concentration in serum was determined by radioimmunoassay (Nichols Institute Diagnostics) with total CV of 6.2% and 5.7% at serum concentrations of 2.05 mg/L and 3.49 mg/L respectively.

Serum cholesterol and triglyceride concentrations were determined with enzymatic methods (Boehringer, Mannheim, Germany). The within-assay CV for total cholesterol and triglyceride determinations was 0.9% and 1.1% respectively.

Fibrinogen was measured according to a syneresis method 23 with a total CV of 4% at 2.5 g/L. Plasminogen activator inhibitor (PAI)-1 activity was measured using a Spectrolyse (pL) PAI kit (Biopool Stabilyte, UmeA, Sweden) with a total CV of 10% at concentrations between 10-40 IU/ml.

Serum insulin was determined by a radioimmunoassay (Phadebas, Pharmacia, Uppsala, Sweden) and blood glucose was measured by the glucose-6-phosphate 10 dehydrogenase method (Kebo Lab, Stockholm, Sweden). Hemoglobin Alc *(HbAlc) was determined by high pressure liquid chromatography (Waters, S" Millipore AB, Sweden) and C-peptide was determined by a radioimmunoassay (Santec, USA). Free fatty acids (FFA) levels were determined using an enzymatic colorimetric method (NEFAC; Wako, Neuss, Germany), while sex hormone 15 binding globulin (SHBG) was measured by an immunoradiometric assay (Farmos, Diagnostica, Abo, Finland) and total testosterone by a radioimmunoassay (ICM, Biomedical, Costa Mesa, USA).

Statistical methods All descriptive statistical results are presented as the means and standard error of the mean (SEM). Comparisons between the two treatment groups were performed by a two-way analysis of variance (ANOVA) for repeated measurements.

Comparisons between baseline values and values at 9 months in the two groups were performed with the Students' t-test for independent groups. Correlations were sought by calculating the Pearson linear correlation coefficient. Pearson's chi square test was used to test the independence of frequency of hypertension and smoking between the rhGH and placebo treated groups. Before statistical analysis.

logaritmic transformation of data with skewed distribution was performed. A twotailed probability value of less than 0.05 was considered significant.

Results The two groups were matched with regard to age, body height, body weight and waist hip ratio, and did not differ significantly regarding number of subjects with medically treated hypertension (Chi sqr.=1.87; p=0.1 7 and current smokers (Chi sqr.=1.2; p=0.

2 7 (Table At baseline the two groups did not differ significantly from each other in any of the variables studied.

B' ody composition The patients' mean overall body mass index and fat-free mass did not change while mean total body fat decreased by 9.2 2.4% during rhGH treatment in comparison with placebo treatment (Figure Waist circumference and sagittal diameter decreased in response to rhGH while no change occurred in the placebo group. Moreover, abdominal subcutaneous and visceral adipose tissue area at the level of L4-5 decreased in response to rhGH by 6.1 3.2% and 18.1 7.6% S: respectively (Figure 1 and Table The corresponding values in the placebo group were +2.0 2.8% and -3.2 7.6% respectively. Moreover, the volume of visceral adipose tissue decreased in the rhGH treated group by 17.9 3.5% while no change was observed in the placebo treated group (Figure 1).

Thus, the percentage of visceral adipose tissue of the total adipose tissue at the level ofL4-5 decreased by 14.5 3.8% ,while the percentage of subcutaneous adipose tissue of the total adipose tissue at the level of L4-5 increased by 5.4 1.7 in the rhGH-treated group.

Abdominal subcutaneous and visceral adipose tissue was determined with computed tomography at the level of L4-5 in one man before and after 9 months of rhGH treatment The scan showed a reduction of both visceral and subcutaneous adipose tissue. (Figure 2) Glucose metabolism No significant effects were elicited by rhGH treatment on blood glucose, serum insulin and HbAlc (Table 3 and Figure The serum concentration of C-peptide increased in the rhGH treated group due to a transient increase at 6 weeks, but the C-peptide level was similar in the two groups at 9 month.

In the rhGH treated group the GDR showed an initial decrease after 6 weeks of treatment followed by an increment while the placebo-treated group o0 demonstrated a slight reduction over time (Figure The average increase in GDR in response to 9 months of rhGH was 1.2 0.7 mg/kg/min compared with baseline while in the group receiving placebo a slight decrease by 0.4 0.6 mg/kg/min occurred. This difference between the two groups was still found .after correcting the GDR for the amount of fat-free mass.

In the rhGH treated group, an inverse correlation was found between the change in GDR and change in serum triglyceride concentration p<0.05) but no significant correlations were found between the change in GDR and changes in serum IGF-I concentration (r=-0.2 4 serum insulin concentration

LPL

activity diastolic blood pressure total body fat and volume of visceral adipose tissue Total cholesterol, triglycerides. LPL activity, plasma fibrinogen and PAl-1 activity (Table 3) The mean total cholesterol concentration decreased from 6.1 0.2 to 5.4 0.3 mmol/L and the triglyceride concentration decreased from 2.09 0.29 to 1.78 0.23 mmol/L in response to rhGH treatment. The corresponding changes in the placebo group were from 5.4 0.3 to 5.5 0.2 mmol/L and from 1.65 0.13 to 2.05 0.26 mmol/L respectively.

The mean total LPL activity in subcutaneous abdominal tissue did not change during rhGH treatment in comparison with placebo treatment. However, between 6 weeks and 9 months, LPL activity tended to increase in the rhGH treated group as compared with the placebo treated group (p=0.0 6 Similar results were obtained when LPL activity was expressed in mU/g TG.

The plasma concentration of fibrinogen increased in response to rhGH while PAI-I activity was unaffected by rhGH treatment as compared with placebo.

10 Blood pressure and heart rate Diastolic blood pressure decreased from 75 2 to 70 2 mmHg in the rhGH treated group. The corresponding values in the placebo group were from 73 2 to 74 2 mmHg No significant effects on systolic blood pressure or heart rate were observed between the two treatment groups.

Serum IGF-I, IGFBP-3. testosterone and SHBG (Table 4) 9* Before treatment, the serum IGF-I concentration was low normal in both treatment groups. A significant increment in serum IGF-I and IGFBP-3 concentrations occurred in the rhGH treated group as compared with placebo treatment. At 6 weeks, the serum IGF-I concentration reached on average 3.30 0.35 SD above the predicted mean in the rhGH treated group while at 9 month the mean serum IGF-I concentration was 1.89 0.48 SD above the predicted mean. Serum concentrations of testosterone and SHBG were not significantly affected by rhGH treatment.

Side-effects No drop-outs occurred during the study. Side-effects were observed in 8 subjects in the rhGH treated group, and were mainly a result of fluid retention. Five had peripheral edema, two subjects experienced muscle stiffness andA arthralgia, one developed mild carpal tunnel syndrome and one subject experienced increased perspiration. These side-effects appeared during the first 6 weeks of treatment and subsided in four patients in response to a reduction in dose performed within 4 months after start of treatment; in three patients, the side-effects subsided spontaneously. One man from the rhGH treated group with medically treated hypertension was taken off treatment after 8 months when he experienced an 0 0i intracerebral hemorrhage. Three subjects in the placebo group experienced slight and transient peripheral edema.

Legends to figures.

Figure 1.

Mean total body fat calculated from total body potassium, abdominal subcutaneous adipose tissue (AT) area at the level of L4-L5 and volume of visceral AT assessed with computerized tomography during 9 months of treatment with 0 rhGH or placebo in 30 men with abdominal /visceral obesity. The horizontal bars indicate the SE for the mean values shown and p-values denotes the differences between the two groups by two-way ANOVA for repeated measurements.

Figure 2.

Abdominal subcutaneous and visceral adipose tissue determined with computed tomography at the level of L4-5 in one man before and after 9 months of rhGH treatment The scan shows the reduction of both visceral and subcutaneous adipose tissue (shown as dark gray area in the figure).

2s Figure 3.

Mean fasting blood glucose, serum insulin and glucose disappearance rate (GDR) assessed with euglycaemic hyperinsulinaemic glucose clamp during 9 months of treatment with rhGH or placebo in 30 men with abdominal/visceral obesity. The horizontal bars indicate the SE for the mean values shown and p-values denotes the differences between the two groups by two-way ANOVA for repeated measurements.

Discussion We have shown that 9 months of rhGH treatment in middle-aged men with 10o abdominal/visceral obesity reduced total body fat and resulted in a specific and marked decrease of both abdominal subcutaneous and visceral adipose tissue.

Insulin sensitivity assessed with euglycemic glucose clamp technique improved and serum concentrations of total cholesterol and triglyceride decreased.

Furthermore, diastolic blood pressure decreased.

15 The men who were studied were moderately obese with a preponderance of abdominal and/or visceral localization of body fat as judged from comparisons with randomly selected men of comparable age from the same city 24. As a group, they had slight to moderate metabolic changes known to be associated with abdominal/visceral obesity with moderate insulin resistant as judged from the GDR values obtained during the euglycemic glucose clamp, although no one had overt diabetes.

Although, we used a lower daily rhGH dose than previously reported in trials studying healthy adults 25, 26, the initial rhGH doses administrated were apparently too high as judged by the frequency of side-effects and initial high average serum IGF-I concentrations. After dose reduction the average serum IGF-I concentration where within the normal range indicating that the doses of rhGH during the latter part of the study were more physiological. This might in turn explain the less marked anabolic action of the rhGH treatment demonstrated in this study in comparison with previous trials in healthy adults 25, 26 The marked effect of GH replacement on body composition in GH-deficient adults has been a consistent observation in many studies 17. The profound lipolytic effect of GH was also demonstrated in the present study with a preferential reduction in visceral adipose tissue depots 27. These changes have been associated with a GHinduced reduction in the antilipolytic effects of insulin, which is markedly different in different adipose tissue regions 28 10 GH exerts direct insulin-antagonistic effects even after the administration of physiological doses of rhGH. GH has been considered to be the principal factor in the decrease in insulin sensitivity observed in the early morning, the so called "dawn phenomenon" 29 and the insulin resistance following hypoglycemia Thus, our observation of increased insulin sensitivity during prolonged rhGH treatment is unexpected. We have previously shown that 6 weeks of rhGH treatment in GH-deficient adults only induced a temporary decrease in insulin sensitivity which after 6 months of treatment was restored to baseline values 31 The response of GDR to rhGH treatment on in this trial showed a similar initial tendency to induce insulin resistance but after 9 months a marked improvement was found.

GH has been found to be an important regulator of the hepatic LDL-receptor 3 and the bverall lipoprotein metabolism 36. The reduction in total cholesterol is conceivable an effect of enhanced hepatic LDL receptor activity in response to

GH

35 In healthy adults, short-term rhGH administration has been reported to increase serum triglyceride concentration 25. In this study, the serum triglyceride concentration also displayed an initial increase in response to rhGH treatment.

This could be an effect of both an increased flux of FFA to the liver and a direct stimulatory effect on the esterification of oleic acid into triglyceride and phospholipids in hepatocytes 37 in response to GH which in turn enhances the very low density lipoprotein production from the liver. However, after 9 months of rhGH treatment serum triglyceride concentration had decreased again, probably as an effect of the increased insulin-stimulated glucose uptake which is known to be inversely related with the very low density lipoprotein secretion rate from the liver and serum triglyceride levels 4.

The initial tendency of a decline in LPL activity observed in the present study is in accordance with a previous 2 weeks treatment trials with rhGH 38. During the 10 more prolonged rhGH treatment, however, LPL activity tended to increase which may, at least in part, explain the decrease in serum triglyceride concentration at 9 months. The changes in GDR and LPL activity showed a similar biphasic pattern in response to GH. It may thus be speculated that the suggested influence of GH on LPL activity is mediated through insulin sensitivity, since insulin is known to 15 be a potent stimulator of LPL.

Nine months of rhGH treatment reduced diastolic blood pressure without affecting systolic blood pressure. This is in line with results from GH-deficient adults where rhGH administration reduced diastolic blood pressure possibly as an effect of reduced peripheral vascular resistance 39. The mechanisms behind the reduction in peripheral vascular resistance might be indirect through the reduced abdominal obesity and increased insulin sensitivity 4 0 or more direct through the action of IGF-I on the vascular wall 41.

Abdominal/visceral obesity is associated with increased plasma fibrinogen concentration and PAI-1 activity 42, 43 which both are established risk factors for myocardial infarction and stroke 44, 45. The slightly increased plasma fibrinogen concentration in response to GH may be mediated through increased serum IGF-I concentration 18. In GH-deficient adults, 2 years of rhGH treatment tended to decrease plasma fibrinogen levels and diminish PAI-1 activity 46. This further illustrates the importance of the duration of rhGH treatment on the metabolic effects of GH.

Previous studies have shown that testosterone treatment of middle-aged men with abdominal/visceral obesity induced improved insulin sensitivity, plasma lipid levels, diastolic blood pressure as well as a specific decrease of visceral adipose tissue mass 14, 46. Since testosterone treatment of men with hypogonadotrophic hypogonadism increases GH secretion 4 7 the similarities between testosterone and rhGH treatment might be explained by increased GH levels or by additive or synergistic effects of GH and testosterone on adipose tissue metabolism 48.

The multiple endocrine alterations associated with abdominal/visceral obesity can either be primary responsible or be the consequence of the obese condition. This is the first trial clearly to demonstrate favorable effects of GH on the multiple perturbations associated with abdominal/visceral obesity. We therefore suggest 15 that a blunted GH secretion could be an important factor in the development of the metabolic and circulatory consequences of abdominal/visceral obesity. The metabolic effects demonstrated in this study are probably of importance for the risk of cardiovascular morbidity and mortality in men with abdominal and central adiposity.

20 The reference to any prior art in this specification is not, and should not be taken as, an acknowledgment or any form of suggestion that that prior art forms part of 'o*o the common general knowledge in Australia.

Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or oup of integers or steps.

Table 1.

Clinical characteristics of the cohort of 30 men treated with GH or placebo for 9 months.

Patient characteristics

GH

Placebo Number of men Mean age (range); years Treated hypertension; no.

Present smokers; no.

Body height; m Body weight; kg Waist hip ratio 16 14 58.3 (48-66) 57.9 (52-63) 2 0 5 2 1.80±0.02 1.77±0.02 101.7±2.4 96.2±2.6 1.01±0.01 1.03±0.02 Plus-minus values are means standard error of the mean.

Table 2.

Measurements of body mass index (BMI), fat free mass, waist circumference, sagittal diameter and abdominal visceral adipose tissue (AT) area at the level of L4-5 in 30 men, during 9 months of rhGH or placebo treatment.

Variable Baseline 6 weeks 6 months 9 months p BMI; kg/m 2 GH 31.4±0.7 31.6±0.7 31.3±0.7 31.1±0.8 0.2 Placebo 30.5±0.8 30.6±0.7 30.5±0.8 30.7±0.8 Fat free mass; kg GH 67.5±1.8 69.7±1.9 71.1±1.8 69.5±2.2 0.4 Placebo 64.6±1.4 65.2±1.4 66.4±1.3 65.3±1.4 Waist; cm GH 111.8±1.8 110.8±1.8 107.6±1.7 109.8±1.9 0.002 Placebo 109.5±2.5 109.4±2.4 109.3±2.3 111.0±2.3 Sagittal diameter;cm GH 26.1±0.5 25.9±0.5 25.2±0.5 25.0±0.6 0.03 Placebo 25.5±0.7 25.3±0.8 24.6±0.9 25.5±0.8 Visceral AT; cm 2 GH 126±15 121±19 98±14 99±15 0.004 Placebo 163±16 147±13 142±12 150±13 All values are expressed as the mean (SEM).

P-values-denote the differences between the two groups by two-way ANOVA for repeated measurements.

Table 3.

Measurements of glycosylated hemoglobin (HbAlc), C-peptide, total cholesterol, triglycerides, lipoprotein lipase (LPL) activity expressed as mU per gram of adipose tissue plasma fibrinogen and plasminogen activator inhibitor (PAI)-1 in men, during 9 months of rhGH or placebo treatment.

S.

V2rw21 Baseline 6 weeks 6 months 9 months HbAlc;

GH

Placebo C-peptide; ng/L

GH

Placebo Total cholesterol; mmolIL

GH

Placebo Triglycerides; mmol/L

GH

Placebo LPL activity; mU/g AT

GH

Placebo Fibrinogen; g1L

GH

Placebo PAl-1 activity; U/mL

GH

Placebo 5.2±0.1 4.9±0.1 1.11±0.10 1.28±0.27 5.2±0.1 5.4±0.1 5.3±0.1 4.9±0.1 5.0±0.1 5.1±0.2 1.60±0O.13 1.30±0O.17 1.30t0.27 1.28±0O.32 1.18±0.07 1.42±0.30 6.1±0.2 5.7±0.2 5.4±0.3 5.6±0O.2 2.09±0.29 2.60±0.42 1.65±0.13 1.80A0.20 6.1±0.2 5.4±0.3 6.1±0.3 5.5±0-2 2.31±0.23 1.78±0-23 1.85±0.22 2.05±0.26 0.8 0.02 0.006 0.02 0.2 0.04 0.4 287±26 224±31 3.13±0O.13 3I03AM1 31.3±6.4 17.0±3.8 205±15 228±29 3.44±0.10 2.73±0.09

ND

ND

3.49±0.13 3.39±0.28 371±65 263±25 3.24±0.19 2.84±0.10 22.9±3.5 27.1±6.3 23.2±+2.6 18.3±3.1 22.9±4.2 19.9±4.5 All values are expressed as the mean (SEM).

P-values denote the differences between the two groups by two-way ANOVA for repeated measurements.

Table 4.

Measurements of serum IGF-I, IGFBP-3, free fatty acids (FFA), testosterone and steroid hormone binding globulin (SHBG) in 30 men, during 9 months of GH/placebo treatment.

I

Variable IGF-I; pg/L

GH

Placebo IGF-I SD score

GH

Placebo IGFBP-3; mg/L

GH

Placebo FFA; nmol/L

GH

Placebo Testosterone; nmol/L

GH

Placebo SHBG; nmol/L

GH

Placebo Baseline 6 weeks 6 months 134±8 338±16 320±23 120±11 121±11 129±12 -0.82±0.17 3.30±0.35 2.91±0.49 -1.07±0.23 -1.04±0.23 -0.87±0.24 2.36±0.13 3.20±0.10 3.19±0.13 2.10±0.16 2.21±0.17 2.45±0.21 0.77±0.07 0.99±0.11 0.78±0.11 0.73±0.05 0.73±0.05 0.59±0.06 14.6±1.2 12.9±1.0 13.9±1.3 14.6±1.0 15.4±1.2 17.6±2.1 26.4±3.4 25.5±3.5 25.9±3.1 28.1±2.9 29.1±3.1 29.2±3.2 9 months p 268±23 119±12 1.89±0.48 -1.08±0.25 2.71±0.14 2.18±0.19 0.75±0.07 0.67±0.05 12.4±1.1 14.6±1.3 23.4±2.8 25.5±2.7 <0.001 <0.001 0.001 0.12 0.8 All values are expressed as the mean (SEM).

P-values denotes the differences between the two groups by two-way ANOVA for repeated measurements.

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Claims (10)

1. 2. Use according to claim 1 wherein said growth hormone is human growth hormone.
2. 3. Use according to claim 1 or claim 2 in which the medicament is for increase of insulin sensitivity.
3. 4. Use according to claiml or claim 2 in which the medicament is for decrease of insulin resistance. Use according to any one of claims 1 to 4 in which the medicament is for a treatment of at least six weeks.
4. 6. Use according to claim 5 wherein said treatment is of more than six months.
5. 9. 7. Use according to claim 5 wherein said treatment is of more than nine months. 8. A method for the treatment of the Metabolic Syndrome and insulin resistance in a non-insulin dependent patient, said method comprising administering to said patient an effective amount of growth hormone or an analogue thereof. 9. The method according to claim 8 wherein said growth hormone is human growth hormone. P:\OPER\Fns\2350440-spc.doc.28/(W)2 -27- The method according to claim 8 or claim 9 in which the treatment is for increase of insulin sensitivity.
6. 11. The method according to claim 8 or claim 9 in which the treatment is for decrease of insulin resistance.
7. 12. The method according to any one of claims 8 to 11 in which the treatment is of at least six weeks.
8. 13. The method according to claim 12 wherein said treatment is of more than six months.
9. 14. The method according to claim 12 wherein said treatment is of more than nine months.
10. 15. A use according to any one of claims 1 to 7 or a method according to any one of claims 8 to 14 substantially as hereinbefore described with reference to the examples. DATED this 1 st day of July 2002 Pharmacia Upjohn AB by DAVIES COLLISON CAVE Patent Attorneys for the Applicants o