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Hypothyroidism, Metabolism and Food Intake

Completed
Conditions
Hypothyroidism
Interventions
Registration Number
NCT02993562
Lead Sponsor
Herlev Hospital
Brief Summary

This project has the following primary aims:

To measure changes in appetite and food intake in newly diagnosed hypothyroid patients during the first six months after starting levothyroxine (L-T4) substitution therapy

Secondary aims are:

To delineate the effect of L-T4 substitution therapy on thyroid status, body weight, body mass index (BMI), body composition, physical activity, glycaemic control, postprandial gut and pancreatic hormone responses, gastric and gall bladder emptying, resting energy expenditure (REE), quality of life (QOL) and cognitive function

Detailed Description

18 newly diagnosed hypothyroid female patients and 18 healthy controls age between 20 and 75 years will be recruited from the out-patients clinic in Herlev and Gentofte Hospital and the general practitioners before start of substitution therapy.

The study is devided in to three identical experimental days of approx. 6 hours. First experimental day placed before T4 treatment is initiated. Second day as soon as Thyroid Stimulating Hormone (TSH) is below 4 milli unit pr liter (mU/l). The Third experimental day after 6 months of T4 therapy.

For 5-7 days before each experimental day, the participants' physical activity energy expenditure (PAEE) will be monitored by an Actiheart® pedometer attached to the skin of the chest.

The last two days before each experimental day, the participants will follow a standardised diet following World Health Organization guidelines on energy requirements and nutrient composition according to gender, age and body weight Shortly after diagnosis patients will undergo a test panel at the first experimental day, where patients arrives fasting.

Visual analog score on satiety and thirst will be filled out continuously. REE will be measured by a CCM-express calorimeter,

* Dual Energy X-ray absorptiometry (DEXA)-scan

* Blood samples will be taken continuously during the experimental day. Gall bladder size will be examined at 6 times during the experimental day using ultra sound.

At the end of the day, patients´ satiety will be examined with an ad libitum meal.

Blood will be analysed for Gastric inhibitory polypeptide (GIP), Glucagon-like Peptide 1 (GLP-1), Glucagon-like Peptide 2 (GLP-2), glucagon, peptide tyrosine tyrosine (PYY), Gastrin, Cholesystokinin (CCK), Insulin, C-peptide, Blood sugar, Cholesterol, Free fatty acids and paracetamol.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
18
Inclusion Criteria
  • TSH > 10
  • Female
Exclusion Criteria
  • Competing serious disease
  • Male
  • Not able to understand written and spoken danish
  • Pregnancy
  • Thyroidectomized patients
  • Amiodarone treatment.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Hypothyroid patientsLevothyroxineHypothyroid patients treated with Levothyroxine as part of normal treatment.
Primary Outcome Measures
NameTimeMethod
Changes in food intake at ad libitum meal6 months

Changes in food intake at ad libitum meal measured at each experimental day

Satiety6 months

Satiety measured on a visual analog score 13 times during each experimental day.

Secondary Outcome Measures
NameTimeMethod
Changes in gall bladder emptying6 months

Changes in gall bladder emptying evaluated with ultrasound 6 times each experimental day before and after meal.

Changes in GLP-1 hormones6 months

Continously measuring of GLP-1 hormones during each experimental day

Changes in CCK hormones6 Months

Continuously measuring of CCK hormones during each experimental day

Changes in Free-Fatty acids6 Months

Continuously measuring of Free Fatty acids during each experimental day

Changes in lean mass assessed through lean mass6 months

Changes in lean mass assessed through lean mass with DEXA-scan

Changes in blood sugar response to standardized meal.6 Months

changes in blood sugar response to standardized meal measured before and after meal at each experimental day.

Changes in Insulin hormones6 Months

Continuously measuring of Insulin during each experimental day

Changes in fat mass assessed through lean mass with DEXA-scan6 months

Changes in lean mass assessed through lean mass with DEXA-scan

Changes in stomach emptying6 months

Evaluated with continously measuring serum paracetamol after standardized meal containing 1,5 g paracetamol.

Changes in GIP hormones6 months

Continously measuring of a range of hormones during each experimental day: GIP

Changes in GLP-2 hormones6 Months

Continuously measuring of GLP-2 hormones during each experimental day

Changes in PYY hormones6 Months

Continuously measuring of PYY hormones during each experimental day

Changes in Glucagon6 Months

Continuously measuring of Glucagon during each experimental day

Changes in resting energy expenditure6 months

Changes in resting energy expenditure measured 3 times each experimental day using Indirect Calorimetry.

Changes in Gastrin hormones6 Months

Continuously measuring of Gastrin during each experimental day

Changes in C-peptide6 Months

Continuously measuring of C-peptide during each experimental day

Trial Locations

Locations (1)

Center for Diabetes Research, Herlev and Gentofte Hospitals

🇩🇰

Copenhagen, Region Hovedstaden, Denmark

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