Night Hyperglycemia and Fatty Liver in Type 1 Diabetes

Sponsor
HaEmek Medical Center, Israel (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT05933018
Collaborator
(none)
120
1
1
18
6.7

Study Details

Study Description

Brief Summary

This clinical trial aims to discover the relationship between hyperglycemia at night and early morning hours and the presence of fatty liver in patients with type 1 diabetes.

The main question it aims to answer are:

• if hyperglycemic patterns related to metabolic parameters in type 1 diabetes The data from the insulin pump and sensor will be processed. The patients will be divided into two groups. One group without night hyperglycemia and the other with night hyperglycemia. Investigators will perform liver elastography for these two groups. The presence or absence of hepatic steatosis will be evaluated in these groups according to the data.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: liver elastography
N/A

Detailed Description

Introduction Normal subjects have well-defined 24-hour cycles of insulin secretion and plasma insulin levels (rising in the early morning, peaking in the afternoon, and declining at night.

The dawn phenomenon is the result of an exaggeration of the physiologic impairment of insulin sensitivity was noted during the early morning hours. During previous studies, no exact explanation of this phenomenon was found. According to the studies, high growth hormone levels with decreased suppression by hyperglycemia, central hypersensitivity to growth hormone-releasing hormone (GHRH), low insulin-like growth factor-I (IGF-I), high insulin-like growth factor-binding protein-1 (IGFBP-1), and peripheral resistance to growth hormone are involved in the pathogenesis of Dawn syndrome. The etiology, prevalence, and consequences of hepatic steatosis in type 1 diabetes remain poorly understood.

Methods The study will include 120 consecutive patients with type 1 diabetes, using an insulin pump and continuous glucose monitoring device treated in our clinic. Investigators will extract the data related to glucose levels and pump programming. The data about glucose levels and insulin requirements during the night hours will be collected. The study participants will be divided into two groups according to the presence or absence of night hyperglycemia. We will perform liver elastography on 100 study patients.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
120 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Interconnection Between Night Hyperglycemia and Fatty Liver in Type 1 Diabetes Mellitus
Actual Study Start Date :
Jan 15, 2023
Anticipated Primary Completion Date :
Jul 15, 2024
Anticipated Study Completion Date :
Jul 15, 2024

Arms and Interventions

Arm Intervention/Treatment
Other: type 1 diabetes

patients with type 1 diabetes underwent liver elastography

Diagnostic Test: liver elastography
the imaging of the liver will perform in the fasting state, in the morning hours by one specialist, dedicated to this procedure,

Outcome Measures

Primary Outcome Measures

  1. to evaluate presence of fatty liver in type 1 diabetes [through study completion, an average of 1 year.]

    Liver fat and fibrosis will be assessed by controlled attenuation parameter (CAP) and liver stiffness measurements (LSM) by FibroScan . The attenuation parameter ( CAP ) >270 db/m will be consistent with fatty liver and liver stiffness > 7 will be consistent with liver fibrosis

Secondary Outcome Measures

  1. presence of metabolic syndrome in type 1 Diabetes Mellitus [through study completion, an average of 1 year]

    presence of metabolic syndrome in patients with type 1 diabetes including elevated BMI, increased waist circumference, presence of elevated triglycerides, presence of hypertension will be evaluated

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • type 1 diabetes patients

  • C- PEPTIDE level <0.6

  • continuous glucose monitoring system

  • insulin pump users

Exclusion Criteria:
  • pregnancy

  • type 2 diabetes

  • non-pump or sensor users

  • unwilling to participate

Contacts and Locations

Locations

Site City State Country Postal Code
1 Emek Medical Center Afula Israel/zaphon Israel 1834160

Sponsors and Collaborators

  • HaEmek Medical Center, Israel

Investigators

  • Principal Investigator: Elena Chertok Shacham, MD, Emek Medical Center

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Elena Chertok, MD, HaEmek Medical Center, Israel
ClinicalTrials.gov Identifier:
NCT05933018
Other Study ID Numbers:
  • 0101-22-EMC
First Posted:
Jul 6, 2023
Last Update Posted:
Jul 6, 2023
Last Verified:
Jul 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Elena Chertok, MD, HaEmek Medical Center, Israel
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 6, 2023