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Study of Human Adipose Tissue (LOSHAT)

Longitudinal Observational Study of Human Adipose Tissue (LOSHAT)

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03675464
Acronym
LOSHAT
Enrollment
1500
Registered
2018-09-18
Start date
2018-09-20
Completion date
2023-12-31
Last updated
2020-09-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adipose Tissue, Human, Lipolysis, Obesity, Type 2 Diabetes Mellitus, Weight Change, Body, Weight Gain, Weight Loss

Brief summary

The investigators will study the influence of initial fat cell size/number and adipose function (in particular lipolysis) on weight development over very long time periods (years). By comparing investigations of fat biopsies or blood samples obtained at baseline, the investigators will determine the association between adipose morphology/function and changes in weight or development of metabolic complications (e.g. metabolic syndrome, glucose intolerance, type 2 diabetes, dyslipidemia and hypertension).

Detailed 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, 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.

Interventions

None listed

Sponsors

Karolinska Institutet
CollaboratorOTHER
Karolinska University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

* Previously participated in examinations at the investigators laboratory and donated adipose tissue. * Previously participated in examinations at the investigators laboratory and donated blood samples that can be used to estimate lipolysis with a formula.

Exclusion criteria

* Decline to participate after invitation. * Severe Psychiatric disease. * Type 1 Diabetes * Participants that have undergone bariatric surgery will be exluded in the primary analysis but will be analyzed separately in a secondary analysis for all above mentioned outcomes.

Design outcomes

Primary

MeasureTime frameDescription
Number of participants with metabolic syndrome2018 to 2022Metabolic syndrome is defined according to International Diabetes Federation, Waist circumference ≥102 cm for men or ≥88 cm for women. In addition to this 2 of the following; Raised triglycerides: \> 150 mg/dL (1.7 mmol/L), or specific treatment for this lipid abnormality; Reduced HDL cholesterol: \< 40 mg/dL (1.03 mmol/L) in males, \< 50 mg/dL (1.29 mmol/L) in females, or specific treatment for this lipid abnormality; Raised blood pressure (BP): systolic BP \> 130 or diastolic BP \>85 mm Hg, or treatment of previously diagnosed hypertension; Raised fasting plasma glucose (FPG): \>100 mg/dL (5.6 mmol/L), or previously diagnosed type 2 diabetes. Scores are 0-5. ≥ 3 is defined as metabolic syndrome.
Body mass index2018 to 2022Body weight (in kilogram) will be assessed with a regular scale. Height will be measured with a tape measure (in centimeters). Body mass index (BMI) will be calculated with the formula weight (kg) divided by height\^2 (in meter). Changes in BMI from baseline values will be analysed.
Fasting glucose2018 to 2022Fasting plasma glucose will be assessed and divided into normal glucose (glucose \< 6.1 mmol/L), impaired fasting glucose (glucose 6.1-6.9 mmol/L) or type 2 diabetes (glucose \> 6.9 mmol/L).
Number of participants with Hypertension2018 to 2022Based on a diagnosis in the Swedish National Patient Register, or prescribed drugs for hypertension in the Swedish National Prescribed Drug Register, or direct information from the subject.
Number of participants with type 2 Diabetes2018 to 2022Based on a diagnosis in the Swedish National Patient Register, or prescribed drugs for Type 2 diabetes in the Swedish National Prescribed Drug Register or direct information from the subject.
Number of participants with dyslipidemia2018 to 2022Based on a diagnosis in the Swedish National Patient Register, or prescribed drugs for dyslipidemia in the Swedish National Prescribed Drug Register, or direct information from the subject.

Secondary

MeasureTime frameDescription
Genetic variations linked to lipolysis2018 to 2022Genome-wide association study (GWAS) with focus on genes related to lipolysis and analysis of single nucleotide polymorphisms (SNPs). Samples from baseline examination will be used in the analysis.

Countries

Sweden

Contacts

Primary ContactPeter Arner, MD, PhD
peter.arner@ki.se+468 58582342
Backup ContactDaniel P Andersson, MD, PhD
daniel.p.andersson@ki.se+468 58580000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026