Copeptin and Nonalcoholic Fatty Liver Disease

NCT ID: NCT03254563

Last Updated: 2021-02-10

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 60 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2018-06-19
• Study Completion Date: 2021-06-30

Brief Summary

Copeptin, a surrogate marker for vasopressin, has been found to be elevated in metabolic disorders including obesity and diabetes, which are disorders both associated with nonalcoholic fatty liver disease (NAFLD), and therefore suggest a potential role for vasopressin in the pathogenesis of NAFLD. The investigators intend to investigate if there is an association of vasopressin with the presence and severity of NAFLD.

Detailed Description

Participants: As a pilot study, the investigators will recruit 30 obese adults with NAFLD based upon ultrasound echogenicity within 6 months of enrollment, and 30 obese adults without NAFLD based upon ultrasound (US) echogenicity for comparison.

Screening Visit/Study Visit: Patients in the investigator's Obesity clinic will be approached about the study and consented if interested at the screening. Participants will have a chart review for their history and physical Exam and medication review for inclusion and exclusion criteria. Qualified participants will be invited for a screening visit to be scheduled in conjunction with the labs and procedures performed as Standard of Care (SOC) in the obesity clinic. At the screening visit, following consent, participants will have vitals (blood pressure, Body Mass Index (BMI), waist circumference) and a physical examination performed. Participants' Standard of Care (SOC) labs including fasting lipid panel, HbA1c (unless done within last 3 months), comprehensive metabolic panel, titers for hepatitis b and c, and complete blood count will be drawn, along with the following research labs: insulin, glucagon, free fatty acids, adiponectin and a 24-hour urine cortisol collection. Those who have not had an abdominal US will have a SOC US performed to delineate non-NAFLD or NAFLD status. US will not be performed if already done within 6 months of enrollment. All ultrasound studies will be interpreted by one University of Colorado Denver radiologist to categorize the patient as NAFLD or non-NAFLD to limit inter-reader variability. Those with NAFLD present on US will also have a SOC Fibroscan done to assess severity of steatosis (based upon Controlled Attenuation Parameter or CAP Score) and fibrosis (based upon elastography). Given limitations of ultrasound to accurately detect significant steatosis unless >30%, the investigators will in addition perform Fibroscan (all particpants regardless of US) to assess steatosis, so as to confirm if significant steatosis and compare copeptin levels on a continuum of level of steatosis as part of research procedure. Fibroscan can detect steatosis (based upon Controlled Attenuation Parameter or CAP Score) and fibrosis (based upon elastography). FIbroscan with M probe has been found to have AUROC 0.823 for a cutoff of value of 248 dB/m for no steatosis vs steatosis (with other cutoffs at 268 dB/m between S1 and S2-S3 and 280 dB/m between S1-S2 and S3 disease).

Conditions

NAFLD

Study Design

• Observational Model Type: OTHER
• Study Time Perspective: CROSS_SECTIONAL

Study Groups

Obese with NAFLD

Patients who have NAFLD based upon ultrasound

No interventions assigned to this group

Obese without NAFLD

Patients who do not have NAFLD based upon ultrasound

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

1. Patients age 30-75

2. BMI 30-40

3. Presence of fatty liver on ultrasound

Exclusion Criteria

1. Diabetes mellitus (determined by prior HbA1c, fasting glucose, and/or random glucose in the last three months according to ADA criteria),

2. Medication known to affect insulin sensitivity e.g. metformin, thiazolidinediones, systemic steroids, atypical antipsychotics),

3. Fibrates,

4. eGFR <45 ml/min/1.73m2 by MDRD equation(11),

5. Pregnancy,

6. Breast feeding,

7. Sodium <135 mEq/L,

8. Diabetes insipidus,

9. Liver disease other than NAFLD (including obstructive liver disease),

10. ALT or AST>60 IU/L,

11. Hepatic steatosis on ultrasound for the non-NAFLD group,

12. Congestive heart failure,

13. Patients who consume >20g of ETOH a day,

14. Patients found to have Cushing's disease based upon 24 hour urine results (Urine Free cortisol >2x upper limit of normal).

15. Patient's with pacemakers

16. Off of Coenzyme Q for 6 months.

• Minimum Eligible Age: 30 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Colorado, Denver

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Thomas Jensen, MD

Role: PRINCIPAL_INVESTIGATOR

University of Colorado, Denver

Locations

University of Colorado

Aurora, Colorado, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

Thomas Jensen, MD

Role: CONTACT

thomas.jensen@ucdenver.edu

7208482650

Kristen Nadeau, MD

Role: CONTACT

Kristen.Nadeau@childrenscolorado.org

(720) 777-6128

Facility Contacts

Thomas Jensen, MD

Role: primary

720-848-2650

Kristen Nadeau, MD

Role: backup

Kristen.Nadeau@childrenscolorado.org

720-777-2855

Other Identifiers

17-1160

Identifier Type: -

Identifier Source: org_study_id