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Completed

NCT Number: NCT01294319

Evaluation of Cortisol Resistance in Young Sedentary and Endurance-Trained Men

This study proposes to examine multiple aspects of the hypothalamic-pituitary-adrenal axis in younger endurance trained and sedentary men, and in older sedentary men.

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Key information

Age range

18 year–80 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 2

Primary location

National Institutes of Health Clinical Center, 9000 Rockville Pike

Bethesda, Maryland, 20892, United States

About this study

Adrenocorticotropin (ACTH) secretion is normally exquisitely regulated through endogenous stimulation by corticotrophin-releasing hormone (CRH) and negative feedback inhibition by cortisol, resulting in a circadian rhythm of cortisol. Recent evidence suggests that older men, and younger men who are endurance-trained athletes, both have reduced sensitivity to negative feedback, and perhaps increased basal levels of cortisol and ACTH. To investigate these possibilities, we propose to examine multiple aspects of the hypothalamic-pituitary-adrenal axis in younger endurance trained and sedentary men, and in older sedentary men.

Subjects will collect saliva during two evenings before additional testing, and will on the same evening collect urine for twelve hours, both for cortisol measurements. Blood samples will be collected to evaluate the response to dexamethasone. We also will assess ACTH and cortisol responses to medications that reduce negative inhibition of ACTH. This testing will occur in the evening and will include administration of the glucocorticoid antagonist mifepristone, the mineralocorticoid antagonist spironolactone, and/or a look-alike tablet, on four occasions.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

  • INCLUSION CRITERIA:

Men aged 18 to 30 years of age are required for the young endurance trained and sedentary groups; men aged 65-80 years for the older study group, who will meet criteria for sedentary men below. Women and children are excluded to enhance homogeneity of responses and avoid the influence of menstrual cyclicity on the HPA axis.

Sedentary:

  • Less than one hour physical activity per week for three years
  • No change in exercise anticipated for 6 weeks

Trained:

  • Greater than 45km (28 miles) running per week for at least 3 months
  • No change in exercise anticipated for 6 weeks

For all participants:

  • All races
  • Sleep-wake cycle with sleeping at night, wakening between 5 and 8 AM
  • BMI between 18 and 25 kg/M2
  • Normal TSH and free T4

Exclusion criteria

For all participants:

  • Sleep disorders as assessed by sleep apnea questionnaire
  • Smoking
  • No more than 2 servings of alcohol daily
  • Medications known to affect the HPA axis or steroid metabolism, including narcotics, Glucocorticoids, megace or CYP3A4 modulators
  • History of psychiatric or endocrine disorders
  • Marijuana or other illicit drug use
  • Recent appendicular or skeletal injury
  • Uncontrolled hypertension
  • Chronic pain requiring daily medication
  • Current treatment with medications related to mineralocorticoid function such as potassium, ACE-inhibitors, ARBs, diuretics, spironolactone
  • Frailty score of 4-7 on the Canadian Study of Health and Aging frailty scale (Rockman 2005)
  • Overtraining syndrome will be an exclusion and will be assessed by questionnaire
  • Abnormal creatinine level (greater than 1.2 mg/dl)
  • Liver function tests greater than two fold normal
  • Benzodiazepine use

Treatment and study plan

Mifepristone

Drug

Other names: Mifepristone 400 MG

Placebo

Drug

Spironolactone

Drug

Other names: Spironolactone 200 MG

Combined

Drug

Other names: Mifepristone 400 MG and Spironolactone 200 MG

Dexamethasone

Drug

Other names: Dexamethasone 0.25 mg

Primary outcomes

  1. Proportion of Suppressors After Dexamethasone

    Time frame: cortisol measured between 8 and 9 after dexamethasone was taken between 11 PM and midnight

    All subjects will take 0.25mg dexamethasone as an outpatient between 2300 and 2400h and will then report to the clinic by 0800h next day for the final visit.

    At the final visit, cortisol response to dexamethasone suppression was assessed. The cortisol response was dichotomized (suppression vs. non-suppression, using 1.8 ug/dL as the cutoff point) and compared between the two groups,Sedentary Young Adults and Endurance-trained Young Athletes.

Secondary outcomes

  1. Post-dexamethasone Cortisol Level

    Time frame: Cortisol obtained at 8-9 AM after dexamethasone taken between 11 pm and midnight

Sponsors and collaborators

Lead sponsor

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Nih

Registry information

Official study title

Evaluation of Cortisol Resistance in Young Sedentary and Endurance-trained Men and Elderly Sedentary Men

Important dates

Study start
2011
Primary completion
2016
Study completion
2016
First posted
Feb 11, 2011
Registry last updated
Jul 15, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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