Eastern Mediterranean Health Journal, Vol. 11, No. 3,

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Eastern Mediterranean Health Journal, Vol. 11, No. 3, 2005 329 Subclinical hypothyroidism in lithiumtreated psychiatric patients in Tehran, Islamic Republic of Iran M. Aliasgharpour, 1 M. Abbassi, 1 H. Shafaroodi 2 and F. Razi 1 ABSTRACT We investigated thyroid function in 46 (20 female & 26 male) psychiatric outpatients on lithium treatment by assessing triiodothyronine, thyroxine and thyroid stimulating hormone (TSH) levels. The presence of thyroid antibodies (anti-thyroid peroxidase and anti-thyroglobulin) was also assessed. Out of the 46 patients, 8 (17%) displayed overt hypothyroidism. Of the remaining patients, subclinical hypothyroidism was found in 16 patients (35%) and euthyroidism in 22 (48%). Thyroid antibodies were present in 6 patients in the euthyroid group and 5 patients in the hypothyroid group. The Pearson product-moment correlation results indicated positive association between TSH level and duration of lithium use and age of the patients with subclinical hypothyroidism. Duration of lithium use and age could be a reasonable indicator for screening asymptomatic patients for subclinical hypothyroidism after starting lithium treatment. Hypothyroïdie infraclinique chez des patients psychiatriques traités au lithium à Téhéran (République islamique d Iran) RÉSUMÉ Nous avons examiné la fonction thyroïdienne chez 46 patients (20 femmes et 26 hommes) des consultations psychiatriques externes traités au lithium en évaluant le taux de triiodothyronine, de thyroxine et de thyréostimuline hypophysaire (TSH). La présence d anticorps anti-thyroïde (anti-thyroperoxydase et anti-thyroglobuline) a également été évaluée. Huit (17 %) des 46 patients présentaient une hypothyroïdie patente. Parmi les patients restants, on a trouvé une hypothyroïdie infraclinique chez 16 d entre eux (35 %) et une euthyroïdie chez 22 (48 %). Des anticorps anti-thyroïde étaient présents chez 6 patients dans le groupe de l euthyroïdie et chez 5 patients dans le groupe de l hypothyroïdie. Les résultats de la corrélation des moments mixtes de Pearson ont indiqué une association positive entre le taux de TSH, la durée de l utilisation du lithium et l âge des patients présentant une hypothyroïdie infraclinique. La durée de l utilisation du lithium et l âge pourraient servir d indicateurs plausibles pour le dépistage de l hypothyroïdie infraclinique chez des patients asymptomatiques après instauration d un traitement au lithium. 1 National Reference Laboratory of Iran, World Health Organization Collaborating Centre, Biochemistry Trace Elements Analysis Laboratory, Bou-Ali Hospital, Tehran, Islamic Republic of Iran (Correspondence to M. Aliasgharpour: mehri9@yahoo.com). 2 Department of Pharmacology, School of Medicine, Azad University of Medical Sciences, Tehran, Islamic Republic of Iran. Received: 09/02/04; accepted: 17/05/04

330 La Revue de Santé de la Méditerranée orientale, Vol. 11, N o 3, 2005 Introduction Lithium carbonate is widely used in the treatment of mood disorders such as bipolar disorder. It has been reported to induce gastrointestinal [1], neuromuscular [2] and endocrine adverse effects [3] in 35% 93% of patients taking it. To optimize its effect, therefore, it is important to be aware of these side-effects. Thyroid hypofunction is one of the most common endocrine sideeffects associated with lithium treatment. In most cases lithium-induced hypothyroidism is subclinical [4 6]. The mechanism of the effect of lithium on the thyroid gland is not fully understood. However, it has been shown that lithium reduces iodine uptake into the gland, inhibits iodine addition to tyrosine, reduces triiodothyronine (T 3 ) and thyroxine (T 4 ) release and enhances thyroid stimulating hormone (TSH) release [5 8]. Furthermore, some studies have reported a higher incidence of thyroid antibodies in patients treated with lithium (24%) compared with those not taking lithium (12%) [9,10]. The risk of lithium-induced antibodies increases with the duration of therapy and is more common in women than in men [9,10]. It has been reported that up to 10% 20% of patients develop lithium-induced subclinical hypothyroidism [11 13]. The majority of these patients have few symptoms or none at all. However, it has been shown that conversion of subclinical hypothyroidism to overt hypothyroidism in the presence of circulating antibodies is high [14]. Therefore, routine screening of patients receiving lithium has been advocated. In this regard, TSH appears to be the most efficient parameter in revealing subclinical hypothyroidism in patients on lithium treatment [11 13]. In the present study we evaluated the possible effect of lithium on thyroid function tests (TSH, T 3 andt 4 levels) in 46 psychiatric outpatients at the Reference Laboratory of the Islamic Republic of Iran in Tehran. Methods Over the 2-year period 2001 2002, a total of 46 (20 female and 26 male) psychiatric outpatients attending the Reference Laboratory to check their serum lithium level were randomly selected for the study. A questionnaire was completed for each patient with the patient s age, any previous thyroid gland problems, time of possible onset and duration of lithium use. All the patients reported that before starting lithium treatment they had had their thyroid tested and the results were normal. Any patients with a previous thyroid disorder were excluded from the study. Thus 5 patients who had had their thyroid gland removed or had a thyroid disorder not associated with lithium use were excluded. To investigate whether lithium is an important risk factor for the development of subclinical hypothyroidism, 95% confidence intervals (95% CI) were calculated. Then the Pearson product-moment correlation was performed to asses whether there was a correlation between pairs of variables such as TSH level, lithium concentration, duration of lithium use and age of patients with subclinical hypothryroidism. Blood samples were drawn 8 10 hours after oral dose/s of lithium were given and sera were separated from the cells within 2 hours. Serum lithium concentration was determined using flame atomic absorption spectroscopy (Varian 20-plus) [15,16]. Sera were sent to the radioimmunoassay (RIA) laboratory for the determination of TSH (K1100To28202, Kavoshyar Iran Co.), T 3 (K1100To38203, Kavoshyar Iran Co.), T 4 (K1100To28203 Kavoshyar Iran

Eastern Mediterranean Health Journal, Vol. 11, No. 3, 2005 331 Co.) levels, as well as anti-thyroid peroxidase (anti-tpo) (Monobind, Inc. Product code: 1125-300, USA) and anti-thyroglobulin (anti-tg) (Monobind, Inc. Product code:1025-300, USA). Results Table 1 gives the patient information. Duration of lithium use varied with a mean of 6 years (standard deviation 4.3) and range of 2 15 years. None of the patients had visible thyroid gland enlargement. Out of the 46 patients, 8 (17%) (4 females and 4 males) displayed overt hypothyroidism. Based on the completed questionnaires they were on levothyroxin and had normal TSH levels. Therefore, no further study was performed on this group of patients. Subclinical hypothyroidism, for which no thyroid supplementation was used, was observed in 16 patients (35%, 95% CI: 23.0% 54.0%) (6 female and 10 males) and euthyroidism was observed in 22 patients (48%) (14 females and 8 males). Of the16 subclinical cases, 5 had mildly elevated TSH levels (TSH 3.0 30 mu/l) and 11 had highly elevated TSH levels (TSH > 30 mu/l): normal TSH levels for adult are 0.5 3.0 mu/l. In both groups, free T 4 levels were normal. We carried out the Pearson productmoment correlation between the TSH level of the 16 patients with subclinical hypothyroidism and lithium concentration, duration of lithium use and age. Significant differences were observed for patient s age (r = 0.71, P < 0.01) and duration of lithium use (r = 0.76, P < 0.001); lithium concentration was not significantly correlated (P > 0.05) (Table 2). Furthermore, using the Fisher exact test there was no significant difference for sex and occurrence of subclinical hypothyroidism (P > 0.05). Thyroid antibodies (anti-tpo and anti- Tg) were present in 6 patients (27%) (5 females and 1 male) in the euthyroid group (n = 22). In addition, 5 patients (31%) (3 females and 2 males) in the subclinical group tested positive for these antibodies (Table 3). Discussion Subclinical hypothyroidism is defined as elevated concentration of TSH and normal level of serum T 4. This disorder in lithiumtreated patients may be present without symptoms [6,11,12,17,18] In the present study thyroid function was evaluated in 46 psychiatric (20 female and 26 male) outpatients with different duration of lithium treatment (2 15 years) and 16 (35%) patients displayed subclinical hypothyroidism after starting lithium treatment. They appeared to be symptom-free and did not complain of any side-effects. Table 1 Patient information Sex Total Mean (SD) No. of Mean No. of Previous number duration of patients with (SD) age patients with thyroid of patients lithium use overt (years) subclinical gland (years) hypothyroidism hypothyroidism disorder Female 20 5.4 (4.3) 4 53 (3) 6 No Male 26 6.3 (4.0) 4 45 (5) 10 No SD = standard deviation.

332 La Revue de Santé de la Méditerranée orientale, Vol. 11, N o 3, 2005 Table 2 Pearson product-moment correlations between variables and thyroid stimulating hormone (TSH) level in the 16 subclinical patients Variable r P-value TSH & age 0.71 0.01 TSH & lithium concentration 0.29 0.28 TSH & lithium duration 0.76 0.001 Since in the normal population the prevalence of subclinical hypothyroidism ranges from 1% to12% [19,20], our results indicate lithium is an important risk factor for the development of subclinical hypothyroidism. Studies have reported the incidence of lithium-induced hypothyroidism increases with the duration of treatment [21]. The mean duration of lithium treatment for our subclinical hypothyroid patients was relatively long at 6 years. Duration of lithium treatment was significantly associated with the risk of increased TSH levels and the development of subclinical hypothyroidism (P < 0.001). In addition, researchers have shown that the incidence of subclinical hypothyroidism increases with age, especially Table 3 Positivity of thyroid autoantibodies in lithium-induced subclinical hypothyroidism and euthyroid cases Thyroid Euthyroid Subclinical autoantibodies in a (n = 22) (n = 16) Females 5 3 Males 1 2 Total (%) 6 (27) 5 (31) a Anti-thyroid peroxidase & anti-thyroglobulin. in women [22]. Our preliminary data indicate a correlation (P < 0.01) between TSH level in subclinical hypothyroid patients and age, but sex was not a significant factor (P > 0.05). Previous studies have indicated the presence of thyroid autoantibodies (24%) in patients receiving lithium is high [9,10]. Furthermore, it has been shown that lithium may accelerate the production of the thyroid autoantibodies that may be present prior to lithium treatment [9]. Singer reported that overt hypothyroidism develops in a high proportion of subclinical cases who have positive thyroid autoantibodies [14]. In our study, 5 subclinical patients (31%) displayed high thyroid autoantibody titres. Our data also indicate that lithiuminduced subclinical hypothyroidism may occur in the absence of thyroid autoantibodies (11 patients) although subclinical patients are at higher risk of developing overt hypothyroidism. Because of our small sample size, antibody positivity by itself was not a good marker for predicting conversion of subclinical hypothyroidism to overt hypothyroidism. Our results indicate that duration of lithium use and age regardless of sex could be a reasonable indicator for screening asymptomatic patients for subclinical hypothyroidism after starting lithium treatment. In addition, TSH appears to be a more suitable parameter for assessing subclinical hypothyroidism than the presence of positive thyroid autoantibodies. Acknowledgements Special thanks go to co-workers in the RIA laboratory, especially Mrs Farahnaz Mehrabi and Dr Gasem Khosravanie for all their help during thyroid panel tests.

Eastern Mediterranean Health Journal, Vol. 11, No. 3, 2005 333 References 1. Birch NJ. Lithium. In: Seiler HG, Sigel H, eds. Handbook on toxicity of inorganic compounds. New York, Marcel Dekker Inc., 1988:383 93. 2. Kocsis JH et al. Neuropsychologic effects of lithium discontinuation. Journal of clinical psychopharmacology, 1993, 13:268 76. 3. Lenox RH et al., eds. American psychiatric press textbook of psychopharmacology, 2nd ed. Washington DC, American Psychiatric Press, 1998:379 429. 4. Ozpoyraz N, Tamam L, Kulan E. Thyroid abnormalities in lithum-treated patients. Advances in therapy, 2002, 19(4):176 84. 5. Bocchetta A et al. Thyroid abnormalities during lithium treatment. Acta psychiatrica Scandinavica, 1991, 83(3): 193 8. 6. Smigan L et al. Lithium therapy and thyroid function tests. A prospective study. Neuropsychobiology, 1984, 11(1):39 43. 7. Salata R, Klein I. Effects of lithium on the endocrine system: a review. Journal of laboratory and clinical medicine, 1987, 110:130 6. 8. Surks MI, Sievert R. Drugs and thyroid function. New England journal of medicine, 1995, 333:1688 94. 9. Lazarus JH. Endocrine and metabolic effects of lithium. New York, Plenum, 1986: 99 124. 10. Deniker P et al. Thyroid autoantibody levels during lithium therapy. Neuropsychobiology, 1978, 4(5):270 5. 11. Bensenor I. Screening for thyroid disorders in asymptomatic adults from Brazilian populations. São Paulo medical journal, 2002, 120(5):146 51. 12. Kleiner J, Altshuler L, Hendrick V, Hershman JM. Lithium induced subclinical hypothyroidism: review of the literature and guidelines for treatment. Journal of clinical psychiatry, 1999, 60(4):249 55. 13. Perrild H et al. Thyriod function and ultrasonically determined thyroid size in patients receiving long-term lithium treatment. American journal of psychiatry, 1990, 147:1518 21. 14. Singer PA et al. Treatment guidelines for patients with hyperthyroidism and hypothyroidism. JAMA: the journal of the American Medical Association, 1995, 273:808 12. 15. Murray RL. Lithium. In: Pesce A, Kaplan LA, eds. Methods in clinical chemistry. St Louis, CV Mosby Co. 1987. 16. Analytical methods (F-AAS). St Helens, Australia, Varian Australia Pty Ltd, 1989 (Publication # 85 10000900). 17. Surks MI, Ocampo E. Subclinical thyroid disease. American journal of medicine, 1996, 100(2):217 23. 18. Cooper DS. Subclinical hypothyroidism. New England journal of medicine, 2001, 345(4):260 5. 19. Tunbridge WMG et al. The spectrum of thyroid disease in a community; the Whickham survey. Clinical endocrinology, 1977, 7:481 93. 20. Canaris GJ et al. The Colorado thyroid disease prevalence study. Archives of internal medicine, 2000, 160:526 34. 21. Transbol I, Christiansen C, Baastrup PC. Endocrine effects of lithium: hypothyroidism, its prevalence in long-term treated patients. Acta endocrinologica, 1978, 87:759 67. 22. Helfand M, Redfern CC. Screening for thyroid disease; an update. Clinical Guideline Part 2. Annals of internal medicine, 1998, 129:144 58.