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Functionality of Endogenous Biological Clock in Sepsis

Functionality of Endogenous Biological Clock in Sepsis

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04063332
Enrollment
60
Registered
2019-08-21
Start date
2019-06-03
Completion date
2024-06-30
Last updated
2023-12-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Circadian Rhythm Disorders, Sepsis

Keywords

circadian, sepsis, clock, melatonin

Brief summary

The aim of the current study is to demonstrate dysregulation of immune system΄s circadian rhythms as a consequence of sepsis, as well as marked malfunction of the central circadian clock in comparison with patients without sepsis , the presence of which burdens independently the final outcome and , hence, need to be addressed.

Detailed description

Sepsis is number one cause of death within the critically ill patients ,with mortality that reaches a rate of 70%,while in case of the establishment of septic shock and multi organ failure it can rise up to 80%.Septic shock is the most common cause of death in the ICUs. It has been estimated that 25% of the total of septic patients will develop severe sepsis (sepsis and organ failure), while septic shock (sepsis and cardiovascular failure). In order to call a biological rhythm circadian, the following 3 criteria must be satisfied: 1. Insistence on stable conditions, with endogenous period of about 24 hours. 2. Independence of ambient temperature, so that almost always progresses at the same rate (same frequency), independent of temperature. 3. This endogenous rhythm, of approximately 24 hours, can be synchronized in exactly 24 hours, influenced by environmental factors, such as light/dark cycles, social interactions, etc. Many organic systems follow a circadian pattern, among others the immune system,on the grounds that peripheral blood lymphocytes own all the forementioned genes, whose coordinated expression with that particular periodicity results in the generation of maximum (peak) and minimum (nadir) of the number of circulating cells, their activity, the production and secretion of cytokines etc.This endogenous attitude is lost in case of sepsis, due to few or absent stimuli deriving from the central clock. As a result, an additional compounding factor comes up in the immune system ,which fails to fight the infectious agent and that inefficient immune response aggravates the circadian desynchronization , creating a vicious circle. The direct evaluation of circadian rhythms' entails the examination of suprachiasmatic neurons' functionality, through biopsies from the examined patients ,which constitutes an ethically questionable ,practically expensive, time-consuming and quite demanding procedure. Thus, the estimation of actual circadian profile will take place indirectly, driven by a series of biomarkers, indicative of the functional status of the ''central biological clock'' found at the suprachiasmatic nucleus of CNS (melatonin, cortisol, core body temperature),as well as the ''peripheral clock'' placed at the immune system cells (Clock/ Bmal1 , Per/Cry genes' expression). The purpose of this prospective, observational, case-control study is to investigate the discrepancy in levels of circadian biomarkers in patients suffering from sepsis in comparison with those coming from other ,non-septic patients in the same environment as well as deviation from healthy controls' values, and secondarily to assess the effect of septic syndrome in later development of endogenous clock that regulates daily life with regard to the quality of life that follows recovery.

Interventions

None listed

Sponsors

Hellenic Sepsis Study Group
CollaboratorOTHER
University of Athens
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Adults (age ≥18 years) * Written informed consent * Male or female gender * Οne of the following cases: * Healthy controls without comorbidities OR * Patients without sepsis or infection , with identical Charlson Comorbidity Index and same mental status with the septic patients OR * Patients with sepsis

Exclusion criteria

* Failure to obtain written informed consent * Age \<18 years * Pregnancy or breastfeeding * Solid tumor or hematologic malignancy * Asthma * Neurodegenerative disease * Traumatic brain injury * Confirmed depression * Autoimmune disorders * Special categories following unfixed or varying routine schedules (e.g. travels overseas or even short distances, if frequent/jet lag/on-call duties/nightshifts with regard to doctors,security guards,singers) * Per os or iv corticosteroids daily intake of dose at least * Corticosteroid oral or intravenous intake of at least 0.4 mg/kg of equivalent prednisone daily over the last 15 days

Design outcomes

Primary

MeasureTime frameDescription
The difference in the extent of deviation from normal, with regard to the levels of circadian rhythms' genes expression (immune system's clock) between septic and non-septic patients ,within their peripheral blood leucocytes .7 daysExtent of abnormality in the mRNA levels of clock, bmal1, per, cry genes within peripheral blood leucocytes.
The substantial discrepancy in the values of melatonin, cortisol and core body temperature (central CLOCK circadian markers) between septic and non-septic patients.7 daysDifferent values in melatonin,cortisol, core body temperature .
The substantial discrepancy in the circadian rhythms' genes expression levels (peripheral clock markers) between septic and non-septic patients ,within their peripheral blood leucocytes .7 daysDifferent mRNA levels of clock, bmal1, per, cry genes within peripheral blood leucocytes.
The difference in the extent of deviation from normal, with regard to the values of melatonin-cortisol-core body temperature (circadian triad) between septic and non-septic patients.7 daysExtent of abnormality in the values of melatonin,cortisol and core body temperature .

Secondary

MeasureTime frameDescription
Mortality rate at 28 days.28 daysDifferences in early (28-day) all-cause mortality rate between septic and matched non-septic patients .
Mortality rate at 90 days.90 daysDifferences in middle term (90-day) all-cause mortality rate between septic and matched non-septic patients.
Munich ChronoType Questionnaire results ,including Mid-sleep, Sleep Duration on both work and free days (MSw, MSf, MSfsc, SLDw, SLDf, SLDØ, chronotype).30 daysRate of circadian physiology restoration, concerning the discharged subgroup which is recovering from sepsis, with regard to daily routine and quality of life.
Pittsburgh Sleep Quality Index (Global PSQI Score).30 daysSum (range 0 to 21) of seven components,each scored 0 (no difficulty) to 3 (severe difficulty).These entail Subjective sleep quality, Sleep latency, duration, efficiency and disturbance, in addition to Use of sleep medication and Daytime dysfunction.

Countries

Greece

Contacts

Primary ContactEvangelos J Giamarellos-Bourboulis, MD, PhD
egiamarel@med.uoa.gr+302107480662
Backup ContactMaria G Kalogridi, MD
mkalogr@med.uoa.gr+302105831916

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026