Hair Cortisol in Asthma or Allergic Rhinitis Treated With Topical Corticosteroids

NCT ID: NCT01839851

Last Updated: 2014-03-11

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 60 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2013-05-31
• Study Completion Date: 2014-12-31

Brief Summary

The purpose of this study is to prospectively examine the relation between topical corticosteroid use and hair cortisol concentration, among patients with moderate persistent asthma or allergic rhinitis. The investigators hypothesize that patients with asthma or allergic rhinitis treated with topical corticosteroids (i.e. inhaled corticosteroids (ICS) or intranasal glucocorticoids (INGC)) have higher levels of hair cortisol after 3 months of treatment than during the 3 months prior to initiation of treatment.

Detailed Description

Inhaled corticosteroids have proven effective in the treatment of asthma, suppressing airway inflammation and reducing bronchial hyper-responsiveness. Beneficial clinical outcomes include fewer asthmatic symptoms, increased lung function, improved asthma-specific quality of life, and fewer asthmatic exacerbations, including severe attacks resulting in hospitalization or death. ICS are commonly used when asthmatic episodes are too frequent or too severe to be controlled solely by short acting beta agonists. ICS have few adverse effects at low to medium doses, which are mainly local effects such as hoarseness and oral thrush. On the other hand, high doses of ICS are associated with systemic effects such as increased risk of skin bruising, cataracts, elevated intraocular pressure and accelerated loss of bone mass. While there is less evidence pointing towards systemic effects of low to medium doses of ICS, several studies have suggested that such an effect exists. One study demonstrated changes in the hypothalamic-pituitary-adrenal (HPA) axis with ICS administration at doses as low as 88 μg of fluticasone per day. Moreover, a study in children showed ICS did not influence basal cortisol levels but significantly reduced peak cortisol and adrenocorticotropic hormone levels.

Hence, the extent of the systemic effect of ICS at high doses and especially at low to medium doses is not fully understood. This is partly due to the nature of most of the systemic side-effects which necessitate long term follow-up of a large population of patients, but also because of technical difficulties in assessing systemic cortisol levels over a prolonged period of time.

A similar clinical conundrum exists with intranasal glucocorticoids (INGC), regarding their systemic effect. INGCs are considered the first-line of medical therapy for allergic rhinitis and are more effective than systemic antihistamines. The most common adverse effects stem from local irritation of the nasal mucosa, while systemic effects are much rarer. The effect of INGC on the HPA axis and growth has been evaluated extensively in children. Most studies, especially those with the second generation agents and recommended doses, showed no or limited HPA suppression. Despite these reassuring data, the adverse effects of INGC can be additive with those of other glucocorticoid preparations for comorbid conditions, and thus caution should be exercised. A handful of studies have demonstrated detrimental effects of INGC therapy on bone mineral density and intraocular pressure. These studies have small sample sizes and have not clearly proven whether these effects result in clinically relevant long term outcomes, such as fractures. As a result, these studies are not reflected in current practice guidelines.

Cortisol levels are routinely determined from blood, salivary or urinary samples However, these methods do not provide information on long term cortisol secretion, accounting for the variability of HPA axis activity. There is a growing pool of evidence that shows that Hair Cortisol Concentration (HCC) examination provides a reliable retrospective estimation of integrated cortisol secretion over a period of several months. Hair grows at a rate of about 1 cm/month, thus 3 cm of hair would give an indication of the cortisol levels over the previous 3 months. HCC correlates with 24h urinary cortisol levels, but not with salivary or serum cortisol, supporting use of HCC as an indicator of cortisol levels over time rather than a point measurement. HCC has been evaluated in several clinical settings in which activity of the HPA axis and cortisol levels over a period of time are of interest. Studies have demonstrated increased levels of hair cortisol in patients with stress as well as in conditions associated with stress such as pregnancy, unemployment, PTSD, alcohol withdrawal, chronic pain and myocardial infarction. Elevated levels of hair cortisol were also shown in Cushing's syndrome, with reduced levels after correction of the disorder.

No study to date has examined the correlation between the use of inhaled or intranasal corticosteroids and levels of cortisol in hair. If such a correlation exists, it would indicate systemic absorption of these topical steroids which in turn would suggest a potential for systemic side effects. In addition, and pending further studies, HCC may serve as a validated test to determine which patients are more prone to systemic side effects, as well as help in assessing compliance.

Conditions

ASTHMA; ALLERGIC RHINITIS

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Study Groups

Asthma

Treatment with any inhaled corticosteroid

Treatment with any inhaled corticosteroid

Intervention Type: DRUG

Use of any inhaled corticosteroid (daily frequency and dose will be registered)

Allergic rhinitis

Treatment with any intranasal glucocorticoid

Treatment with any intranasal glucocorticoid

Intervention Type: DRUG

Use of any inhaled intranasal glucocorticoid (daily dose and frequency will be registered)

Asthma and allergic rhinitis

Inhaled corticosteroid + intranasal glucocorticoid

Treatment with any inhaled corticosteroid

Intervention Type: DRUG

Use of any inhaled corticosteroid (daily frequency and dose will be registered)

Treatment with any intranasal glucocorticoid

Intervention Type: DRUG

Use of any inhaled intranasal glucocorticoid (daily dose and frequency will be registered)

Interventions

Treatment with any inhaled corticosteroid

Use of any inhaled corticosteroid (daily frequency and dose will be registered)

Intervention Type: DRUG

Treatment with any intranasal glucocorticoid

Use of any inhaled intranasal glucocorticoid (daily dose and frequency will be registered)

Intervention Type: DRUG

Other Intervention Names

Symbicort; Budicort; Qvar; Steronase

Eligibility Criteria

Inclusion Criteria

• Age of 18 years or older
• Diagnosis of asthma or allergic rhinitis, or both.
• Planned initiation of treatment with ICS and/or INGC at study recruitment, according to routine clinical practice

Exclusion Criteria

• Use of inhaled, systemic or topical corticosteroids at study initiation, or during the previous 6 months.
• Use of topical corticosteroid ointments or cream, or systemic corticosteroids during the study period.
• Disorders associated with disruption of HPA axis (Cushing syndrome, Addison syndrome).
• Insufficient hair for analysis
• Bleaching or use of artificial hair color.
• Pregnancy

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Meir Medical Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Eilon Krashin, MD

Role: PRINCIPAL_INVESTIGATOR

Meir Medical Center

Locations

Meir Medical Center

Kfar Saba, , Israel

Site Status: RECRUITING

Countries

Israel

Central Contacts

Eilon Krashin, MD

Role: CONTACT

eilon.krashin@clalit.org.il

972-50-4233063

Leader Avi, MD

Role: CONTACT

avi.leader@clalit.org.il

References

Stalder T, Kirschbaum C. Analysis of cortisol in hair--state of the art and future directions. Brain Behav Immun. 2012 Oct;26(7):1019-29. doi: 10.1016/j.bbi.2012.02.002. Epub 2012 Feb 15.

Reference Type: BACKGROUND

PMID: 22366690 (View on PubMed)

Other Identifiers

MMC-13-0047-CTIL

Identifier Type: -

Identifier Source: org_study_id