Enrolling by invitation

Phosphodiesterase 3B's Role in Adipose Tissue and Metabolic Health

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What is being collected

Data Collection

Collected at a single point in time - Cross-sectional
DNA Samples
Who is being recruted

Cardiovascular Diseases+7

+ Diabetes Mellitus

+ Diabetes Mellitus, Type 2

From 21 to 75 Years
See all eligibility criteria
How is the trial designed

Case-Control

Comparing exposures between individuals with and without disease in order to identify potential risk factors.
Observational
Study Start: September 2025
See protocol details

Summary

Principal SponsorCambridge University Hospitals NHS Foundation Trust
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: September 1, 2025

Actual date on which the first participant was enrolled.

This study explores the role of a protein called Phosphodiesterase 3B (PDE3B), which is involved in how the body processes nutrients like sugars and fats. Researchers have discovered that some people with a specific genetic change affecting PDE3B might be less likely to develop diabetes and heart disease. The study aims to understand the role of PDE3B in fat tissue function and its impact on blood sugar and fat levels. By understanding these processes better, the study could lead to new strategies to prevent or manage diabetes and heart disease. Participants in the study will include both those with the genetic variant affecting PDE3B and those with the usual gene type. The study involves two visits. The first is a 4-hour screening where participants undergo a medical check-up, blood tests before and after consuming a sugary drink, and assessments of lifestyle factors like physical activity, sleep, and diet. For those eligible, a 24-hour visit includes an insulin infusion and collection of blood and fat tissue samples. The main focus is to measure lipolysis, which is how the body breaks down fats, using a special technique involving stable isotope tracers. This research could provide valuable insights into how PDE3B influences nutrient handling in the body and help develop preventive measures for related diseases.

Official TitleThe Role of Phosphodiesterase 3B in the Regulation of Human Adipose Tissue Biology and Systemic Glucose and Lipid Homeostasis
Principal SponsorCambridge University Hospitals NHS Foundation Trust
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

40 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Case-Control

These studies compare people who have a disease (cases) with those who don't (controls). The goal is to look back at previous exposures or risk factors to identify what might have contributed to the disease.


Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 21 to 75 Years

Range of ages for which participants are eligible to join.

Conditions

Pathology

Cardiovascular DiseasesDiabetes MellitusDiabetes Mellitus, Type 2Endocrine System DiseasesHyperinsulinismInsulin ResistanceMetabolic DiseasesNutritional and Metabolic DiseasesMetabolic SyndromeGlucose Metabolism Disorders

Criteria

Inclusion Criteria: * willing and able to give informed consent for participation in the study * aged 21-75 years * men and women Exclusion Criteria: * unstable weight (\>5% change the last 2 months) * type 2 diabetes or other major organ dysfunction * cancer in last 5 years * gastrointestinal or bariatric surgery (except cholecystectomy and appendectomy) * conditions that render subject unable to complete all testing procedures (including individuals with known allergies or contraindications to the medications used in this study) * use of medications that affect the study outcome measures or increase the risk of study procedures and that cannot be temporarily discontinued * smoking * illegal drug use * pregnant or lactating * unable to grant voluntary informed consent or comply with the study instructions

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Cambridge University Hospital

Cambridge, United KingdomOpen Cambridge University Hospital in Google Maps
Enrolling by invitationOne Study Center