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Aromatase Inhibitors and Weight Loss in Severely Obese Men With Hypogonadism

Phase 4
Recruiting
Conditions
Hypogonadism, Hypogonadotropic
Obesity
Interventions
Registration Number
NCT03490513
Lead Sponsor
Baylor College of Medicine
Brief Summary

The investigators have preliminary data suggesting that obese patients with hypogonadotropic hypogonadism (HHG) have minimal benefit from testosterone therapy likely because of its conversion to estradiol by the abundant aromatase enzyme in the adipocytes. The increased conversion of androgens into estrogens in obese men results in a negative feedback of high estradiol levels on hypothalamus and pituitary, inhibiting the production of gonadotropin-releasing hormone (GnRH), luteinizing hormone (LH) and follicle stimulating hormone (FSH) and, as a consequence, of testosterone by the testis. Testosterone administration could increase estradiol production, further promoting the inhibitory feedback to the hypothalamic-pituitary-gonadal axis. Although weight loss from lifestyle modification has been shown to reduce estradiol and increase testosterone levels, the effect is at best modest and weight regain results in recurrence of hypogonadism. The use of aromatase inhibitors, in combination with weight loss, could be an effective alternative strategy due to its action at the pathophysiology of the disease.

Intervention Subjects (body mass index of ≥35, testosterone \<300 ng/dl) will be randomized to the active (anastrozole) or control (placebo) group. Anastrozole 1 mg tablet / day will be self-administered with or without food, at around the same time every day (active group); placebo 1 tablet/day with or without food to take at around the same time every day (control group). The study duration will be 12 months.

Both groups will undergo lifestyle intervention consisting of diet and supervised exercise program. Target weight loss will be at least 10% of baseline body weight during the intervention. Subjects will attend weekly group behavior modification sessions which will last \~75-90 min for the first 3 months and decreased to every two weeks from 3 to 12 months. Subjects will attend supervised research center-based exercise sessions during the first 6 months followed by community fitness center-based sessions during the next 6 months for at least 2 d/wk, with recording of home-based exercises for the other 2-4 days/week.

Detailed Description

After age of 40, testosterone (T) production in men gradually decreases at a rate of 1.6% per year for total and to 2-3% per year for bioavailable T. This reduction in T production in men parallels the age-associated loss of muscle mass that leads to sarcopenia and impairment of function and the age-associated loss of bone mass that leads to osteopenia and fracture risk.

Hypogonadism is a condition associated with multiple symptom complex including fatigue, depressed mood, osteoporosis, gain of fat mass, loss of libido and reduced muscle strength, all of which deeply affect patient quality of life. The prevalence of hypogonadism among obese men was estimated to be as much as 40% and could as much as 50% if they are also diabetic, with levels of androgens decreasing proportionately to the degree of obesity.

In obese men, the age-related decline in T is exacerbated by the suppression of the hypothalamic-pituitary-gonadal axis by hyperestrogenemia. The high expression of aromatase enzyme in the adipose tissue enhances the conversion of androgens into estrogens which in turn exerts a negative feedback on hypothalamus and pituitary, inhibiting the production of gonadotropin-releasing hormone (GnRH), luteinizing hormone (LH) and follicle stimulating hormone (FSH) and, as a consequence, of T by the testis resulting in hypogonadotropic hypogonadism (HH). Considering the high aromatase expression in the adipose tissue, the administration of T among obese men with HHG could increase the conversion of the substrate T to estradiol (E2) and fuels the negative feedback on hypothalamus and pituitary, producing a greater suppression of GnRH and gonadotropins. Thus, men with obesity induced HHG may benefit from other treatment strategies that target the pathophysiology of the disease.

Although weight loss intervention improves hormonal and metabolic abnormalities related to obesity, the increase in T levels induced by weight loss are often lost due to weight regain, which is very frequent among patients undergoing massive weight loss. One possible approach is the use of aromatase inhibitors (AI) to stop the conversion of T to E2 thereby interrupting the vicious cycle of E2 inhibition of the hypothalamic-pituitary-gonadal axis and restoring T production to normal levels. Since weight loss remains the standard of care for obese patients, the investigators propose the following OBJECTIVES:

1. To evaluate the effect of an AI plus WL (AI+WL) compared to WL alone on the changes in hormonal profile in severely obese men with HHG.

2. To evaluate the effect of an AI+WL compared to WL alone on the changes in muscle strength and muscle mass, and symptoms of hypogonadism in severely obese men with HHG.

3. To evaluate the effect of an AI+WL compared to WL alone on the changes in body composition and metabolic risk factors in severely obese men with HHG.

4. To evaluate the effect of an AI+WL compared to WL alone on the changes in bone mineral density (BMD), bone markers, and bone quality in severely obese men with HHG.

As secondary aim, the investigators will elucidate the mechanism for the anticipated positive effects of AI+WL on obesity-associated HHG.

This is a randomized double-blind placebo-controlled study comparing the effect of weight loss + anastrozole to weight loss + placebo for 12 months on the hormonal profile and symptoms associated with hypogonadism in severely obese men with a body mass index (BMI) of more or equal to 35 kg/m2.

Recruitment & Eligibility

Status
RECRUITING
Sex
Male
Target Recruitment
120
Inclusion Criteria
  • obese men with body mass index (BMI) of ≥35 kg/m2
  • age between 40 to 65 years old
  • average fasting testosterone level from 2 measurements taken between 8 to 10 AM on 2 separate days of <300 ng/dl
  • Luteinizing Hormone (LH) of <9.0 mIU/L
  • Estradiol of ≥17 pg/ml
  • Symptoms consistent with androgen deficiency as assessed by Androgen Deficiency in Aging Male (ADAM) questionnaire

Exclusion criteria:

  • pituitary or hypothalamic disease,
  • drugs affecting gonadal hormone levels, production and action or bone metabolism (bisphosphonates, teriparatide, denosumab, glucocorticoids, phenytoin)
  • diseases affecting bone metabolism (e.g. hyperparathyroidism, untreated hyperthyroidism, osteomalacia, chronic liver disease, significant renal failure, hypercortisolism, malabsorption, immobilization, Paget's disease),
  • prostate carcinoma or elevated serum prostate specific antigen (PSA)> 4 ng/ml,
  • Hematocrit > 50%,
  • untreated severe obstructive sleep apnea,
  • Cardiopulmonary disease (e.g. recent myocardial infarction, unstable angina, stroke) or unstable disease (e.g., New York Heart Association Class III or IV congestive heart failure
  • severe pulmonary disease requiring steroid pills or the use of supplemental oxygen (that would contraindicate exercise or dietary restriction)
  • History of deep vein thrombosis or pulmonary embolism
  • severe lower urinary tract or prostate symptoms with International Prostate Symptom Score (IPSS) above 19
  • excessive alcohol or substance abuse
  • unstable weight (i.e. >±2 kg) in the last 3 months
  • condition that could prevent from completing the study
  • screening bone mineral density (BMD) T-score of <-2.0 at the spine, femoral neck or total femur
  • history of osteoporosis or fragility fracture
  • Diabetes mellitus with a fasting blood glucose of >140 mg/dl, and/or Hemoglobin A1C (A1C) >8.5%.
Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Weight loss plus placeboPlaceboParticipants will take a placebo every day, attend behavioral classes conducted by a dietitian, receive instruction on how to loss 10% of their body weight and undergo supervised exercise training program.
Weight loss plus anastrozoleanastrozole (1 mg/day)Participants will take Anastrozole 1mg per day, attend behavioral classes conducted by a dietitian, receive instruction on how to loss 10% of their body weight and undergo supervised exercise training program.
Primary Outcome Measures
NameTimeMethod
Hormonal Profile Changes12 months

Assessed by changes in serum testosterone levels.

Changes in muscle strength12 months

Assessed by changes in knee extension strength using a dynamometer.

Changes in total hip bone mineral density (BMD)12 months

Assessed by dual energy absorptiometry.

Changes in Lean mass12 months

Assessed by body composition tissue measurement using dual energy x-ray absorptiometry.

Secondary Outcome Measures
NameTimeMethod
Other gonadal hormone12 months

Assessed by changes in serum estradiol

Pituitary hormone12 months

Assessed by changes in serum follicle stimulating hormone (FSH)

Changes in thigh muscle volume12 months

Assessed magnetic resonance imaging of both thighs.

Changes in symptoms of hypogonadism12 months

Assessed by the 36-Item Short-Form Health Survey (SF-36) questionnaire; scores on the physical and mental component subscales of the SF-36 range from 0 to 100, with higher scores indicating better health status

Changes in visceral adipose tissues12 months

Assessed by dual energy x-ray absorptiometry

Changes in metabolic risk factors12 months

Assessed by homeostasis model assessment for insulin resistance (HOMA-IR)

Changes in volumetric bone density12 months

Assessed by high-resolution peripheral quantitative computer tomography

Changes in bone quality12 months

Assessed by changes in finite element analysis using high-resolution peripheral quantitative computer tomography

Changes in bone markers12 months

Assessed by serum procollagen 1 Intact N-terminal

Trial Locations

Locations (1)

Michael E. DeBakey VAMC

🇺🇸

Houston, Texas, United States

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