Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Adipose Tissue
  • Human
  • Lipolysis
  • Obesity
  • Type 2 Diabetes Mellitus
  • Weight Change, Body
  • Weight Gain
  • Weight Loss
Type
Observational
Design
Observational Model: CohortTime Perspective: Prospective

Participation Requirements

Age
Between 18 years and 90 years
Gender
Both males and females

Description

The investigators will ask all subjects that have previously been examined at the investigators laboratory (from 1992 and forward) in studies of adipose tissue function if they are interested to participate in a new study. Previously obtained results from examinations of adipose tissue, anthropometr...

The investigators will ask all subjects that have previously been examined at the investigators laboratory (from 1992 and forward) in studies of adipose tissue function if they are interested to participate in a new study. Previously obtained results from examinations of adipose tissue, anthropometric measurements and blood samples will be used as baseline. In addition, saved blood samples and samples from old fat biopsies can be re-investigated in some cases. The new investigation includes a questionnaire that the subjects can answer by mail or email. In addition, anthropometric measurements and blood pressure determination will be performed at a primary health care center and blood samples will be collected for analysis of fasting glucose, HbA1C and lipids. Information regarding all previously investigated subjects will also be collected from several Swedish national patient registries such as the Patient Register, Prescribed Drug register and Cause-of Death register.

Tracking Information

NCT #
NCT03675464
Collaborators
Karolinska Institutet
Investigators
Principal Investigator: Peter Arner, MD, PhD Karolinska University Hospital Study Director: Daniel P Andersson, MD, PhD Karolinska University Hospital Study Chair: Mikael Rydén, Md, PhD Karolinska University Hospital