Effects of Thyroid Hormone Enzyme Blocking on Hypothyroidism
| Status: | Completed |
|---|---|
| Conditions: | Endocrine |
| Therapuetic Areas: | Endocrinology |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 11/30/2013 |
| Start Date: | January 2013 |
| End Date: | September 2014 |
| Contact: | Joyce D Linderman, R.N. |
| Email: | lindermanj@mail.nih.gov |
| Phone: | (301) 451-7006 |
Effects of Pharmacologic Block of Type-1 Deiodinase on Thyroid Hormone Action and on the Circulating Levels of T3 in Hypothyroid Patients
Background:
- Hypothyroidism is a condition caused by the loss of function of the thyroid gland. The
thyroid gland produces two hormones, T4 and T3. These hormones control the metabolism and
function of many organs. Lack of energy, depression, and constipation are common symptoms of
hypothyroidism. T4 is converted into T3, the active form of thyroid hormone, by two enzymes
called deiodinases. People with hypothyroidism are treated with a synthetic T4 hormone,
which the enzymes convert to T3. This treatment is usually effective, but some people
continue to have symptoms even after treatment. Some researchers think that this may be
caused by a problem with the enzymes that convert T4 into T3. They want to look at how the
enzymes regulate the levels of T4 and T3 in the blood. They will do so by using a drug that
blocks the action of one of the two enzymes.
Objectives:
- To look at how thyroid hormone enzyme blocking affects hypothyroidism treatment
medication.
Eligibility:
- Individuals at least 18 years of age who have hypothyroidism and are on thyroid hormone
replacement therapy.
Design:
- The study consists of one screening visit, 9 days of inpatient hospital admission, and
a follow-up visit 2 weeks after discharge.
- Participants will be screened with a physical exam and medical history. They will
provide blood samples.
- Participants will receive balanced-diet meals to take home for the 2 days before they
enter the hospital. They will continue this diet while in the hospital.
- During the inpatient stay, participants will be monitored with regular blood tests.
They will have the following procedures:
- Continued thyroid hormone replacement for all 9 days.
- Drug to block thyroid enzyme for 7 days.
- Metabolism test, with room temperature changes, on days 1, 2, 5, 8, and 9.
- Measurements of body fat on days 2, 5, and 8.
- Blood glucose tests on days 1 and 9.
- Muscle contraction tests on days 1, 2, 4, 5, 8, and 9.
- Heart imaging studies on days 2, 5, and 8.
- Optional skeletal muscle and fat tissue biopsies on days 1 and 9.
- There will be a follow-up visit 2 weeks after leaving the hospital. Participants will
have a final physical exam and provide blood samples.
Thyroid hormone action is an important regulator of the metabolism and the function of many
organs. The active form of thyroid hormone is T3, and its blood and tissue levels are the
result of the secretion of T3 and its precursor, thyroxine (T4), from the thyroid gland, of
the peripheral conversion of T4 into T3, and of the degradation of these hormones. In
hypothyroid patients (particularly patients who underwent total thyroidectomy), the levels
of T3 are entirely dependent on the exogenously administered T4 (Levothyroxine, L-T4) which
is converted to T3 or to the inactive form, rT3, by enzymes called deiodinases. This complex
system has only been partially studied in humans and very little is known about the
correlation between circulating levels of T3 and end-organ target tissue thyroid hormone
action.
The aim of this protocol is to characterize the contribution of the two activating
deiodinases (type-1 and type-2) to the blood levels and biological effects of T3. To achieve
this goal we intend to study hypothyroid patients treated with adequate replacement of L-T4
therapy while simultaneously blocking the activity of the type-1 deiodinase with
propylthiouracil (PTU).
Twenty hypothyroid patients who underwent total thyroidectomy or are affected by
hypothyroidism and are on L-T4 therapy with normal TSH values will be recruited. After
enrollment in the study, the patients' eligibility will be determined during an outpatient
visit. Patients will be admitted to the NIH Clinical Center for a 9-day period and will
receive PTU at a dose of 200 mg four times daily for seven days. During the hospitalization
for this research protocol, the following studies will be performed: serial blood sampling
for circulating thyroid hormones to obtain pharmacokinetic parameters of T3, lipids, glucose
and insulin; body composition; resting energy expenditure at room temperature and during
exposure to mild cold; echocardiogram and EKG; skeletal muscle strength measurement and
cardiac MRI.
The results obtained from this study will help in further characterizing the effects of
thyroid hormone on metabolism, and may lead to important information on how to optimize the
thyroid hormone replacement therapy for the treatment of hypothyroidism.
- PARTICIPANT INCLUSION CRITERIA:
Study subjects will be adults older than 18 years who do not have any endogenous thyroid
hormone production (i.e. status post total thyroidectomy, or in individuals who have a
residual remnant greater than 2 mL, an uptake in the thyroid gland less than 5% while on
therapy on 123I uptake scan) and on L-T4 replacement at a minimum dose of 1.6 microg/Kg in
a steady state of euthyroidism.
EXCLUSION CRITERIA:
1. Thyroid uptake > 5% at 24 hours on (123)I thyroid scan while on replacement therapy
(in patients with thyroid gland residue > 2 mL by ultrasound).
2. Patients who have lipid disorders requiring pharmacologic intervention.
3. Any elevation of AST or ALT above upper limit of normal range.
4. Any reduction of the WBC count below the lower limit of normal range.
5. History of, and/or current diabetes mellitus (fasting glucose > 126 mg/dL or current
pharmacologic treatment).
6. Hypertension requiring pharmacologic intervention.
7. Female patients who are on hormonal contraceptives or are breastfeeding.
8. Use of beta blocker medications and amiodarone.
9. Pregnancy (women of child-bearing age must have a negative pregnancy test prior to
inclusion).
10. History of vasculitis, viral hepatitis (except A), granulocytopenia.
11. Known allergy or serious adverse event to PTU.
12. Current use of prescription medication or certain non-prescription medications and
dietary supplements known to affect thyroid function and/or metabolism, or alter the
pharmacokinetics of PTU. Should study volunteers receive other pharmacologic
interventions a clinical pharmacist will be consulted to evaluate potential drug-drug
interactions.
13. Presence of persistent diarrhea or malabsorption syndromes that would interfere with
the patient's ability to adequately absorb medications.
14. Inability to obtain venous access for sample collection, or basal hemoglobin of less
than or equal to 12 g/dl.
We found this trial at
1
site
9000 Rockville Pike
Bethesda, Maryland 20892
Bethesda, Maryland 20892
301-496-4000
National Institutes of Health Clinical Center The National Institutes of Health (NIH) Clinical Center in...
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