Omega-3 Fatty Acids Supplementation Improves Early-stage Diabetic Nephropathy and Subclinical Atherosclerosis in Pediatric Patients With Type 1 Diabetes

Sponsor
Ain Shams University (Other)
Overall Status
Completed
CT.gov ID
NCT05980026
Collaborator
(none)
70
1
2
12.1
5.8

Study Details

Study Description

Brief Summary

The investigators conducted this randomized-controlled trial to assess the effect of oral omega-3 supplementation on glycemic control, lipid profile, albuminuria level, kidney injury molecule-1 (KIM-1) and carotid intima media thickness (CIMT) to participants who were pediatric patients with T1DM and diabetic nephropathy.

Condition or Disease Intervention/Treatment Phase
  • Drug: oral omega-3 fatty acids supplementation
  • Dietary Supplement: Placebo
N/A

Detailed Description

Management of diabetic kidney disease (DKD) mainly consists of correction of hyperglycemia, hypertension and dyslipidemia as well as modification of lifestyle. Primary prevention represents prevention from normoalbuminuria to microalbuminuria, while secondary prevention represents prevention from microalbuminuria to macroalbuminuria. Multiple interventional managements with control of blood glucose, blood pressure and lipid, and smoking cessation can significantly improve the prognosis of cardiovascular events and slow down the progression of renal disease.

Omega-3 fatty acids are polyunsaturated fatty acids (PUFAs) derived from fish oil. Numerous studies have evaluated the potential beneficial effects of omega-3 fatty acids on inflammatory, autoimmune, and renal diseases. Due to their anti-inflammatory effects, omega-3 fatty acids have been suggested to protect against kidney damage. Omega-3 fatty acids can reduce proteinuria in patients with chronic glomerular disease and slow immunoglobulin A (IgA) nephropathy. However, the information about the effects of omega-3 fatty acids on kidney function, particularly in diabetic kidney disease still lacks consensus .

No previous study assessed the role of omega-3 fatty acids in diabetes associated complications in particular diabetic nephropathy and subclinical atherosclerosis among pediatric patients with T1DM and there is insufficient evidence to recommend its supplementation for those patients. Therefore, the investigators conducted this study to investigate the role of omega-3 fatty acids as an adjuvant therapy for participants who had diabetic nephropathy in children and adolescents with T1DM and assess its relation glycemic control, microalbuminuria, kidney injury molecule-1, lipid levels and carotid intima media thickness as an index for subclinical atherosclerosis.

Study Design

Study Type:
Interventional
Actual Enrollment :
70 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Omega-3 Fatty Acids Supplementation Improves Early-stage Diabetic Nephropathy and Subclinical Atherosclerosis in Pediatric Patients With Type 1 Diabetes
Actual Study Start Date :
Jan 10, 2022
Actual Primary Completion Date :
Dec 17, 2022
Actual Study Completion Date :
Jan 14, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: oral omega-3 fatty acids supplementation

Intervention group included pediatric patients with diabetic nephropathy receiving oral omega-3 fatty acids supplementation on a daily basis.

Drug: oral omega-3 fatty acids supplementation
oral omega-3 fatty acids supplementation

Placebo Comparator: Placebo comparator

Placebo group or control patients received placebo that were similar in appearance to omega 3 fatty acids and the administered dose was as the same schedule as omega 3 fatty acids.

Dietary Supplement: Placebo
Patients in placebo group received placebo that were similar in appearance to omega 3 fatty acids and the administered dose was as the same schedule as omega 3 fatty acids.

Outcome Measures

Primary Outcome Measures

  1. change in UACR (mg/g creatinine) level [6 months]

    Urinary albumin excretion rate(mg/g creatinine)

Secondary Outcome Measures

  1. change in KIM-1 level (ng/mL) [6 months]

    KIM-1 level((ng/mL)

  2. change in HbA1c(%) [6 months]

    HbA1c%

Eligibility Criteria

Criteria

Ages Eligible for Study:
12 Years to 18 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • patients with T1DM on regular insulin therapy.

  • age from 12 to 18 years.

  • disease duration at least 5 years.

  • having diabetic nephropathy in the form of microalbuminuria (urinary albumin excretion [UAE] 30-299 mg/g creatinine).

  • hemoglobin A1c (HbA1c) ≤8.5% (69 mmol/mol).

  • persistent microalbuminuria was confirmed by abnormal two or three urine samples over a 3- to 6-months period prior to the study despite angiotensin converting enzyme inhibitors (ACE-Is)

Exclusion Criteria:
  • patients with any clinical evidence of infection.

  • patients with renal impairment due to causes other than diabetes.

  • other diabetic complications than nephropathy.

  • elevated liver enzymes.

  • hyper- or hypo-thyroidism.

  • intake of any vitamins or food supplements one month before study.

  • participation in a previous investigational drug study within the three months preceding screening.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Nancy Elbarbary Cairo Egypt 11361

Sponsors and Collaborators

  • Ain Shams University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Nancy Samir Elbarbary, Prof. of Pediatrics, Ain Shams University
ClinicalTrials.gov Identifier:
NCT05980026
Other Study ID Numbers:
  • Ain shams Pediatrics 202021
First Posted:
Aug 7, 2023
Last Update Posted:
Aug 7, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 7, 2023