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Role of 12-lipoxygenase in Platelet Reactivity and Type 2 Diabetes Mellitus

Primary Purpose

Thrombosis, Type 2 Diabetes Mellitus

Status
Completed
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
Primrose oil
Fish Oil
Sponsored by
University of Michigan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Thrombosis focused on measuring platelets, 12-lipoxygenase, fatty acids, DGLA, DHA, EPA, 12-LOX

Eligibility Criteria

21 Years - 70 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Healthy subjects and T2DM patients
  • Postmenopausal women with T2DM
  • All races and ethnicities
  • T2DM patients taking 1st line diabetic treatment (i.e. Metformin)

Exclusion Criteria:

  • Fish and plant oil supplements 2 months prior to enrollment
  • NSAIDS and aspirin 1 week prior to enrollment
  • Cardiovascular event within 6 months prior to enrollment
  • Other anti-platelet treatment including PDE and P2Y12 inhibitors

Sites / Locations

  • University of Michigan

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Active Comparator

Active Comparator

Arm Label

Healthy subjects for Omega-6 protection

T2DM patients for Omega-6 protection

Healthy control for Omega-3 protection

T2DM for Omega-3 protection

Arm Description

Platelets from healthy donors will be assessed for regulation by Primrose Oil (omega-6 fatty acid).

platelets from Type 2 diabetes mellitus (T2DM) patients will be assessed for regulation by Primrose Oil (omega-6 fatty acid).

Platelets from healthy donors will be assessed for regulation by Fish Oil (omega-3 fatty acid).

platelets from Type 2 diabetes mellitus (T2DM) patients will be assessed for regulation by Fish Oil (omega-3 fatty acid).

Outcomes

Primary Outcome Measures

platelet reactivity
decreased platelet activity ex vivo translating to protection from clot formation in vivo

Secondary Outcome Measures

fatty acid incorporation
measure altered levels of essential fatty acids in blood and platelets following treatment
Oxylipin production
determine the oxylipin products formed following each intervention

Full Information

First Posted
January 14, 2015
Last Updated
July 28, 2021
Sponsor
University of Michigan
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
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1. Study Identification

Unique Protocol Identification Number
NCT02629497
Brief Title
Role of 12-lipoxygenase in Platelet Reactivity and Type 2 Diabetes Mellitus
Official Title
Role of 12-lipoxygenase in Platelet Reactivity and Type 2 Diabetes Mellitus
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Completed
Study Start Date
November 2015 (undefined)
Primary Completion Date
June 2017 (Actual)
Study Completion Date
June 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Michigan
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study investigates the potential protective effects of fatty acid supplementation through inhibition of platelet activation. fatty acids (omega-3 and omega-6) will be evaluated for protection from agonist-mediated platelet activation in platelets from type 2 diabetics and healthy controls. Post-menopausal women with type 2 diabetes mellitus and healthy post-menopausal women will be treated with omega-3 and omega-6 fatty acid supplements to determine protection from platelet activation and thrombosis in this high risk population.
Detailed Description
Essential fatty acids such as omega-3 and omega-6 have been shown to play important roles in regulating platelet activation, but the underlying mechanisms have not been fully elucidated as well as their true protection from thrombosis. 12-lipoxygenase oxidized fatty acids are known to play both a pro- and anti-thrombotic effect on platelets depending on the fatty acid. oxidation of arachidonic acid by 12-lipoxygenase resuts in a pro-thrombotic bioactive lipid whereas oxidation of the omega-6 fatty acid DGLA found in plant oil results in formation of a potent anti-thrombotic bioactive lipid. Determining the extent of protection from this and other bioactive lipids produced through oxygenase activity will allow for a better understanding of which fatty acid supplementation may best protect from thrombosis. Essential fatty acids such as omega-3 (DHA/EPA) and omega-6 (DGLA) appear to be protective. However the underlying mechanism for this potential protection is not well understood. Identifying the mechanism by which these supplements protect from platelet activation may identify new approaches to preventing thrombotic events in this high risk population.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Thrombosis, Type 2 Diabetes Mellitus
Keywords
platelets, 12-lipoxygenase, fatty acids, DGLA, DHA, EPA, 12-LOX

7. Study Design

Primary Purpose
Basic Science
Study Phase
Early Phase 1
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
90 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Healthy subjects for Omega-6 protection
Arm Type
Experimental
Arm Description
Platelets from healthy donors will be assessed for regulation by Primrose Oil (omega-6 fatty acid).
Arm Title
T2DM patients for Omega-6 protection
Arm Type
Experimental
Arm Description
platelets from Type 2 diabetes mellitus (T2DM) patients will be assessed for regulation by Primrose Oil (omega-6 fatty acid).
Arm Title
Healthy control for Omega-3 protection
Arm Type
Active Comparator
Arm Description
Platelets from healthy donors will be assessed for regulation by Fish Oil (omega-3 fatty acid).
Arm Title
T2DM for Omega-3 protection
Arm Type
Active Comparator
Arm Description
platelets from Type 2 diabetes mellitus (T2DM) patients will be assessed for regulation by Fish Oil (omega-3 fatty acid).
Intervention Type
Dietary Supplement
Intervention Name(s)
Primrose oil
Intervention Description
T2DM patients and matched controls subjects will be given Primrose oil for 2 months, followed by 2-week washout. Blood will be drawn at the beginning, during, and following treatments and platelet function will be assessed.
Intervention Type
Dietary Supplement
Intervention Name(s)
Fish Oil
Other Intervention Name(s)
DHA/EPA
Intervention Description
T2DM patients and matched controls subjects will be given Fish oil for 2 months, followed by 2-week washout. Blood will be drawn at the beginning, during, and following treatments and platelet function will be assessed.
Primary Outcome Measure Information:
Title
platelet reactivity
Description
decreased platelet activity ex vivo translating to protection from clot formation in vivo
Time Frame
through study completion, an average of 1 year
Secondary Outcome Measure Information:
Title
fatty acid incorporation
Description
measure altered levels of essential fatty acids in blood and platelets following treatment
Time Frame
through study completion, an average of 1 year
Title
Oxylipin production
Description
determine the oxylipin products formed following each intervention
Time Frame
through study completion, an average of 1 year

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy subjects and T2DM patients Postmenopausal women with T2DM All races and ethnicities T2DM patients taking 1st line diabetic treatment (i.e. Metformin) Exclusion Criteria: Fish and plant oil supplements 2 months prior to enrollment NSAIDS and aspirin 1 week prior to enrollment Cardiovascular event within 6 months prior to enrollment Other anti-platelet treatment including PDE and P2Y12 inhibitors
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael A Holinstat, PhD
Organizational Affiliation
University of Michigan
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Michigan
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35791734
Citation
Yamaguchi A, Stanger L, Freedman JC, Prieur A, Thav R, Tena J, Holman TR, Holinstat M. Supplementation with omega-3 or omega-6 fatty acids attenuates platelet reactivity in postmenopausal women. Clin Transl Sci. 2022 Oct;15(10):2378-2391. doi: 10.1111/cts.13366. Epub 2022 Jul 25.
Results Reference
derived

Learn more about this trial

Role of 12-lipoxygenase in Platelet Reactivity and Type 2 Diabetes Mellitus

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