Challenging the Inflammatory Response System in Insomnia Disorder

Completed

Conditions: Insomnia

Interventions: Behavioral: Cold Pressor Test

Registration Number: NCT02261597

Lead Sponsor: Beth Israel Deaconess Medical Center

Brief Summary: The main purpose of this study is to understand how insomnia (compared to good sleep) may affect the response of the body to a repeated physiological challenge, such as inserting the hand in ice-cold water for several times in a row. In particular, the investigators are interested in the response of markers that can be associated with stress, such as blood pressure and stress hormones.

Detailed Description: Sleep is critical for the regulation and maintenance of biological systems, and sleep deficiency, such as insomnia, has been shown to be associated with elevated risks for cardiovascular, metabolic, and mood disorders.

Despite the high prevalence of insomnia in the population, the investigators understanding of the biological consequences of the disorder with respect to inflammatory, autonomic, and stress system markers is limited, and often not consistent.

In addition, insomnia may not only alter the basal activity of these systems, but may change their reactivity to other stressors and challenges. In support of this assumption are findings showing that poor sleep quality in healthy individuals is associated with a stronger biological response to a stressful challenge, such as the cold pressor test. This test involves the immersion of the hand in ice-cold water. It is one of the most commonly used laboratory physiological challenge tests, provoking not only unpleasantness, but also increases in stress and inflammatory markers.

Investigations of such system's reactivity to challenge may elucidate systems abnormalities that the investigators do not capture by only assessing basal system's levels. For example, in patients with rheumatoid arthritis, basal inflammatory levels are normal, but the response to a physiological stress challenge (cold pressor test) is amplified.

To the investigators knowledge, no studies have measured how insomnia may affect the reactivity of biological systems to a stressful challenge, which may serve as an important indicator of system's dysregulation and associated disease risk.

In this light, the primary goal of this proposal will investigate whether stress-related systems are more reactive to a physiological stressful challenge in insomnia disorder compared to healthy controls.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 44

Inclusion Criteria

Women and men between the ages 18-55 years
Blood chemistry in the normal range
BMI less than or equal to 35

Specific to insomnia group:

Diagnosis of insomnia disorder based on DSM-V criteria

Specific for control group:

Good quality and quantity sleep

Exclusion Criteria

Active infection/disease.
History of neurological, chronic pain, immune, cardiovascular, liver/kidney, or metabolic disorder
History of psychiatric disorders within the last 6 months prior to study start
Sleep disorders other than insomnia
Reynaud's disease
Psychotropic, sleep, or any other medications or herbs interfering with the inflammatory, autonomic, or HPA system in the last 2 weeks prior to study start, except oral contraceptives
In psychotherapy or any other behavioral interventions at study start
Donation of blood or platelets within 3 months of hospital visits
Pregnant/nursing.
Substance abuse.

Study & Design

Study Type: OBSERVATIONAL

Study Design: Not specified

Arm && Interventions

Group	Intervention	Description
Insomnia Disorder	Cold Pressor Test	Testing reactivity of stress-related systems to repeated exposure to the cold pressor test (hand immersion into ice-cold water) among participants with a clinical diagnosis of insomnia disorder.
Healthy Control	Cold Pressor Test	Testing reactivity of stress-related systems to repeated exposure to the cold pressor test (hand immersion into ice-cold water) among healthy participants without a diagnosis of insomnia disorder.

Primary Outcome Measures

Name	Time	Method
Stress Reactivity to Physiological Challenge- Change in Serum Levels of Cortisol	Baseline blood was obtained between 11am-12pm and prior to any Cold Pressor Tests (CPTs). Three CPTs were performed, with 1.5 hours between each one. The first CPT was done at 1pm. Blood draws were obtained 20min and 50 min after each CPT.	HPA marker: Change in serum cortisol levels (ug/dL)
Inflammatory Response to Physiological Challenge- Change in Plasma Levels of IL-6	Baseline blood was obtained between 11am-12pm and prior to any Cold Pressor Tests (CPTs). Three CPTs were performed, with 1.5 hours between each one. The first CPT was done at 1pm. Blood draws were obtained 20min and 50 min after each CPT.	Inflammatory marker: Change in plasma levels of IL-6 (pg/mL).

Secondary Outcome Measures

Name	Time	Method
Glucocorticoid Sensitivity- Percentage of IL-6 Positive Monocytes	Monocytes are only obtained from the baseline blood draw, which occurs at 11am.	Percentage of IL-6 positive monocytes following stimulation with LPS (100pg/mL) and varying concentrations of Dexamethasone