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The epidemiological and clinical aspects of adult-onset hypothyroidism
was evaluated by Vargas and co-workers (Lima, Peru). They
have, retrospectively, analyzed 208 patients (females 179, males 29) with
a mean age of 44.7 years. In this cohort the majority of patients were
40-50y old. The diagnosis of primary hypothyroidism was established in
202 patients and only 6 cases were secondary to hypothalamic-pituitary
disorders. The major cause for diminished thyroid function were a previous
history of treated Graves' disease (27.1%), thyroidectomy for other reasons
(10.7%) and thyroid dysgenesis (2.5%). The authors could not find a definite
cause in 125 patients, assuming an association with autoimune disorders.
Treatment of myxedematous pre-coma was evaluated by Diaz
and co-workers from Buenos Aires, Argentina. Three old patients
(2 females, one male, age > 70y) were admitted to the hospital during the
winter with a clinical picture of severe hypothyroidism and a pre-comatous
state (Glasgow score 8/15). Treatment was started with hemodynamic procedures,
LT4 (0.1 mg per day, i.v.) and 300 mg of hydrocortisone.
One patient had chronic atrial fibrillation and cardiac failure. All three
patients had signs and symptoms of acute respiratory infection (treated
with antibiotics). Serum TSH was elevated 44.5-57.6 µU/mL and mean
serum total T4 very low 1.92 µg/dL. All patients
were maintained on the same doses of LT4 and on assisted
ventilatory respiration and recovered fully. The authors argue that low
doses of LT4 are efficient in treating myxedematous
pre-coma.
Subclinical hypothyroidism in infertility and sterility was evaluated
by Sciovra et al. from Buenos Aires, Argentina. A cohort
of 73 females complaining of infertility or sterility was evaluated (infertility
18, sterility 55), with a mean age of 31.2y (21-44). Goiter was present
in 8 patients. Serum TSH levels were in the normal range in 72 patients
(98.6%) but the TSH response to TRH disclosed 8 patients with an exaggerated
response of TSH. In this group, in 2 patients anti-TPO autoantibodies were
present in the serum.
The authors comment that evaluation of thyroid function should be conducted
in all patients complaining of infertility or sterility.
The actual doses of LT4 for treatment of primary
hypothyroidism was discussed by Escobar, from Bogota,
Colombia. The author analyzed, retrospectively, 76 patients with primary
hypothyroidism (ages between 11-68 years) with an initial serum TSH level
between 5.1 and 270 µU/mL. The patients were started on a LT4
doses of 1.3 µg/kg/day. In 51 patients the mean LT4
doses to maintain serum TSH within the normal range was 1.1 µg/kg/day.
However, individuals with very elevated initial serum TSH levels (> 20
µU/mL) needed a higher LT4 daily doses (1.6
µg/kg/day). Also older patients (> 50y) needed a lower LT4
doses (0.9 µg/kg/day). Only 9 patients needed a LT4
dosis higher than 150 µg/day. The authors concluded that LT4
treatment should be individualized and kept at the lower possible doses
to keep serum TSH within normal range.
The impact of subclinical hypothyroidism in clinical practice
was discussed by de la Torre and colleagues from Quito, Ecuador.
They retrospectively analyzed the records of patients seen between 1991-1995
in a general hospital. All patients with serum TSH higher than 4.5 µU/mL
or, alternatively, with a TSH response to TRH higher than 27 µU/mL
were considered as possible candidates for subclinical hypothyroidism.
A total of 495 patients were analyzed who met one of the above criteria.
In these patients the final diagnosis of actual hypothyroidism was made
in 47% of the patients either with goiter or without. A number of other
pathologies was associated with subclinical hypothyroidism such as Turner's
syndrome, dyslipidemias, growth retardation and menstrual disorders. The
authors claim that systematic evaluation of subclinical hypothyroidism
should be proposed for the adult population of a general hospital.
The influence of iodinated desinfectants (I.D.) on TSH values in
screening for congenital hypothyroidism was evaluated by Dratler
and colleagues from Buenos Aires, Argentina. TSH was measured in
dried blood spots (DBS) collected on filter paper by a immunofluorometric
assay (DELFIA) and the results were expressed as µU/mL of serum (cut-off
value 20 µU/mL of serum). Group 1) DBS samples from a NICU (neonates)
population: n = 161; ages (days, X ± SD) 19.2 ± 22.4, range
= 0 to 104; weight (grams, X ± SD) 264 ± 962.4. Within group
1, 65/161 patients were exposed to iodinated disinfectant (ID) (Group 1a)
and 69/161 patients were not exposed to ID (Group 1b). In 27/161 data of
ID-exposure were not available. The degree of iodine exposure was registered
as: a) only one exposure; b) repeated exposures; c) exposed body surface:
25%, 50%, or > 50%. A group of DBS samples from a screening program was
considered as control. (Group 2), n = 748. The results were as follows:
TSH (X ± SD): Group 1: 4.4 ± 4.; range: 1.1 to 25.6; Group
1a: 5.1 ± 5.4; range: 1.1 to 25.6; Group 1b: 4.3 ± 3.5; range:
1.1 to 21.4. (G1a vs. G1b): p: ns. G2: 2.7 ± 2.2; range: 0.5 to
15.5 (G1 vs. G2); 2p <0.001. Group 1 was also evaluated according to
prematurity, weight (<="1500" or> 1500 grams), age (<= 24 or> 24
hrs), diagnosis and presence of illness. Age was the only factor with significant
influence on the TSH levels in the NICU population (p <0.01). Three
cases in Group 1 had higher values than the cutoff level: G 1a: 2/65 (20.4
and 25.6) and G 1b: 1/69 (21.4). (G 1a vs. G 1b): Fisher Exact Test: ns.
The 69 patients without reference to ID use had all normal TSH values.
The authors concluded that: 1) TSH levels were not significatively different
between exposed and not exposed to ID groups in the neonates. 2) Even if
the neonate population as a whole showed significantly higher TSH values
than the control population, they were independent of the use and extent
of ID exposure. 3) Prematurity, weight or presence of illness do not influence
TSH values neither in exposed nor in non-exposed patients. 4) As expected,
the DBS samples obtained within the first 24 hrs of life showed higher
TSH values in the neonate population, exposed or not to ID. Therefore,
use of ID would not be a risk factor to elevate TSH levels above the cutoff
level in congenital hypothyroidism screening in the neonate population.
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