Neurocognitive and Metabolic Effects of Mild Hypothyroidism
Information source: Oregon Health and Science University
Information obtained from ClinicalTrials.gov on November 03, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Hypothyroidism
Intervention: L-thyroxine (L-T4) (Drug)
Phase: N/A
Status: Not yet recruiting
Sponsored by: Oregon Health and Science University Official(s) and/or principal investigator(s): Mary Samuels, MD, Principal Investigator, Affiliation: Oregon Health and Science University
Summary
Patients with hypothyroidism are routinely treated with thyroid hormone (l-thyroxine) for
replacement therapy. Physicians monitor the thyroid hormone dose by measuring a thyroid
stimulating hormone (TSH) level in the blood, with the goal of a normal level. However,
recent data suggest that the "normal" TSH range is too broad, and that patients may still
have symptoms if their TSH levels are at the top or bottom part of the normal range.
To study this issue, it is useful to address issues such as general health status,
psychological symptoms, mood, memory, and metabolic status, since thyroid hormone has major
effects on the brain adn metabolism, and since patients with treated hypothyroidism often
have symptoms related to these areas.
In the present study, otherwise healthy subjects with treated hypothyroidism, ages 20-60
years, will be enrolled in a 6-month study. At baseline, they will have tests of health
status, psychological symptoms, mood, memory, body composition, and energy expenditure
performed. Following these baseline measurements, subjects will receive either their usual
doses of l-thyroxine, or a slightly higher or lower dose. The doses will be chosen to try to
achieve either a low-normal TSH level, a high-normal TSH level, or a mildly elevated TSH
level. Which target TSH the patient is assigned will be determined randomly, and neither the
subject nor the study contacts will know which dose the patient is receiving. Subjects will
be seen every 6 weeks during the study for brief visits to make sure they are not having any
side effects, and to adjust the l-thyroxine doses if the TSH has not yet reached the target
range. At the 24-week visit (end of study), the subjects will undergo the same tests that
they had on the baseline visit.
Results from the study will be examined to see if minor changes in TSH or other thyroid
hormone levels cause changes in any of the outcomes, and if the degree of TSH change
correlates with the degree of outcome changes. These results may help physicians caring for
patients with thyroid disease better determine the optimal dose of thyroid hormone for each
patient.
Clinical Details
Official title: Neurocognitive and Metabolic Effects of Mild Hypothyroidism
Study design: Treatment, Randomized, Double Blind (Subject, Investigator), Dose Comparison, Parallel Assignment
Primary outcome: Cognitive measures, quality of life, mood assessed by the SCL-90R, SF-36, and/or POMS subscales. Metabolic outcomes assessed by DEXA, indirect calorimetry
Secondary outcome: To assess whether changes in cognition or mood depend upon REE and other body composition measures.
Eligibility
Minimum age: 20 Years.
Maximum age: 75 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Ages 20-75
- Primary hypothyroidism on stable dose of L-T4 for > 3 months
- Documented elevated TSH off L-T4
- Normal TSH level on usual dose of L-T4 No acute or chronic medical or psychiatric
illnesses that affect thyroid function, mood or cognition No medication use that
affects thyroid function, mood or cognition (oral contraceptives or estrogen therapy
allowed)
- Normal score on screening MMSE (to test for dementia)
- Normal vision by screening examination
- Normal hearing by screening examination
Exclusion Criteria:
- Failure to meet any of the above inclusion criteria
- Inability to speak and comprehend English
- A history of coronary artery disease
- Screening hgb <10
- Screening wbc > 10,000
- Clinically significant abnormalities on screening metabolic set
- Screening LDL cholesterol > 160
- Screening triglyceride > 300
- Significant abnormalities on screening ECG
- Pregnancy or intent to become pregnant in next 6 months
- Present or recent use of medications that affect thyroid hormone levels or interfere
with thyroid hormone effects, including beta-blockers, lithium, glucocorticoids, or
iodine containing agents
- MMSE score < 26
Locations and Contacts
Oregon Health and Science University, Portland, Oregon 97201, United States
Additional Information
Starting date: June 2008
Ending date: June 2010
Last updated: June 5, 2008
|