Neurocognitive and Metabolic Effects of Mild Hypothyroidism
Hypothyroidism
About this trial
This is an interventional treatment trial for Hypothyroidism focused on measuring Hypothyroidism, Cognition, Metabolism
Eligibility 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 Mini-Mental State Exam (MMSE) (to test for dementia)
- Normal vision by screening examination
- Normal hearing by screening examination
- Non smoker
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
Sites / Locations
- Oregon Health and Science University
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Experimental
1 (Low-normal TSH target)
2 (High-normal TSH target)
3 (Mildly elevated TSH target)
Treatment arm 1 targets a thyroid stimulating hormone (TSH) of 0.28 -2.49 milliunits/liter (mU/L) (the theoretical optimal range). The intervention is as follows: Levothyroxine (L-T4) doses will be adjusted in this arm to achieve this target TSH range. L-T4 is the intervention. L-T4 is given once per day, in the morning, while fasted. Dose ranges for the study are calculated based on each subject's TSH levels monitored during the study. Duration of the intervention is the duration of the study, after which subjects return to taking their usual L-T4 doses.
Treatment arm 2 targeting a TSH of 2.5 - 5.0 mU/L. The intervention is as follows: Levothyroxine (L-T4) doses will be adjusted in this arm to achieve this target TSH range. L-T4 is the intervention. L-T4 is given once per day, in the morning, while fasted. Dose ranges for the study are calculated based on each subject's TSH levels monitored during the study. Duration of the intervention is the duration of the study, after which subjects return to taking their usual L-T4 doses.
Treatment arm 3 is targeting a TSH level o f 5.1-12.0 mU/L. The intervention is as follows: Levothyroxine (L-T4) doses will be adjusted in this arm to achieve this target TSH range. L-T4 is the intervention. L-T4 is given once per day, in the morning, while fasted. Dose ranges for the study are calculated based on each subject's TSH levels monitored during the study. Duration of the intervention is the duration of the study, after which subjects return to taking their usual L-T4 doses.