Free amino acids together with copper, iron and zinc were measured in sera of 67 adult patients with thyrotoxicosis (n = 29) or hypothyroidism (n = 38). In contradistinction to the almost indifferences exhibited by the three metals, many amino acids displayed significant relationships with the thyrometabolic activity (mainly tyrosine and arginine with r values of 0.5 and 0.44, respectively). Additional analyses revealed certain patterns, between trace metals and amino acids, which conferred challenging difficulties to interpretation. Thus while zinc was associated positively with some amino acids (such as glutamic acid and alanine), copper correlated almost invariably in a negative manner with citrulline, alpha-amino-butyric acid, proline, glycine and valine. This new information should contribute to our knowledge of the complex metabolism of both trace metals and amino acids.

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The standard thyrotropin releasing hormone (TRH) test (200 μg) with synthetic TRH is no longer used commonly for the detection of primary hypothyroidism or hyperthyroidism. The reason has been that this test has been replaced by the development of more sensitive thyroid-stimulating hormone (TSH) assays, and hence suppression or elevation of TSH has been regarded as a sufficient criterion for the diagnosis of thyroid dysfunction in conjunction with measurements of free thyroid hormones. 1In the late 1990s it was recognized that depressed subjects with a normal serum TSH could have an exaggerated response to TRH stimulation. For the first time it was suggested that this could be evidence of a very mild degree of subclinical hypothyroidism that could not be diagnosed reliably with screening TSH alone. 2 In 1999, it was again suggested that hypothyroidism is an ongoing disease state starting with only a positive TRH test followed by TSH elevations and progressing to overt hypothyroidism and thyroid hormone failure. Indeed, these authors coined the term sub-biochemical hypothyroidism to denote this earliest phase of primary hypothyroidism in which serum free T4 and TSH levels are still within the reference range but the TRH response is exaggerated similar to established primary hypothyroidism. 3 Finally, in 2005, these observations were extended to pediatric subjects. 4 Again the authors concluded that if there is a goiter and serum TSH is in the upper half of the normal range, a TRH test is necessary to exclude hypothyroidism since basal TSH might not be enough to diagnose this earliest phase of subclinical hypothyroidism. We thus decided to look into a similar group of subjects with normal baseline TSH to see if these findings were reproducible in our population of patients.We retrieved records of TRH testing from our radioimmunoassay lab computer database that was performed between 2001 and 2005. Patients were referred to our dynamic testing facility for a TRH test if there was a strong suspicion of hypothyroidism, despite a normal basal TSH (either low [suggestive of central hypothyroidism] or low-normal free T4 [FT4] with suggestive clinical features). The patients were then followed in the endocrinology clinic, and those patients with an exaggerated response to TRH were considered, based on the individual merits of the case, for therapy along the lines of primary hypothyroidism. We did not evaluate response to therapy, but no patient started

i Summary: A radioassay for the measurement of cortisol binding capacity in human serum was developed and the results validated by radioimmuiioassay of serum corticosteroid binding globulin. The mini-scale method is simple, reliable and rapid, and avoids Separation of partitioned phases. The linear correlation between the free cortisol index and free cortisol concentration äs calculated by the two methods utilizing serum samples with normal and abnormal protein concentrations was r = 0.962 (n = 114, p < 0.001) and the regression equation was y = 3.51 6 -2.632. The teehnique requires no preparation of reagents, and the assay can be performed in 45 minutes using 0.05 ml of serum or plasma.