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Occurrence of hashimoto thyroiditis among the first- and second-degree relatives of systemic lupus erythematosus patients with Hashimoto thyroiditis

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Reumatismo 4/2013 203 letter to the editor

Reumatismo, 2013; 65 (4): 203-204

Occurrence of Hashimoto thyroiditis among

the first- and second-degree relatives

of systemic lupus erythematosus patients

with Hashimoto thyroiditis

L. Carli, C. Tani, S. Vagnani, F. Querci, C. Baldini, R. Talarico, A. Della Rossa, S. Bombardieri, M. Mosca

Rheumatology Unit, University of Pisa, Italy

Corresponding author: Marta Mosca Rheumatology Unit University of Pisa

Via Roma, 67 - 56126 Pisa, Italy E-mail: marta.mosca@med.unipi.it

Sirs,

A number of studies have suggested that thyroid disorders, including Hashimoto thyroiditis (HT), are more frequent in SLE than in general population, with a reported prevalence ranging from 3.9 to 24% (1, 2). Since a genetic background has been de-scribed for systemic autoimmune diseases as well as for autoimmune thyroid dis-eases (AITD), and familial aggregation of systemic autoimmune diseases and AITD has been described (3-6), we have hypoth-esized that first and second degree relatives of systemic lupus erythematosus (SLE) pa-tients with HT might have an increased risk of developing this condition.

The clinical charts of patients with SLE were examined, to identify which subjects suffered from HT, based on the presence of positive thyroid antibodies and ultrasound assessment suggestive of an inflammatory disease.

Patients were asked about the presence of thyroid disorders in their first- and second-degree relatives, using a structured ques-tionnaire, designed ad hoc for this study (Appendix).

We considered valid the presence of HT when the patient reported specifically that diagnosis.

The clinical charts of 401 SLE patients (371 female, 30 male) were examined. Six-ty-eight (17%), 65 women and 3 men had a diagnosis of HT, 12 were lost to follow-up. Of the remaining 56, 28 (50%) had at least one first- or second-degree relative with a thyroid disease. A total of 36 relatives (30

women, 6 men) with a thyroid dysfunction were observed. Eight were affected by HT, 8 by MNG, while the diagnosis was un-clear in 20 relatives, with 19 cases (53% of the total number of relatives) with hypo-thyroidism and 1 case of hyperhypo-thyroidism. Two relatives were reported to have had a history of papillary carcinoma.

Hashimoto thyroiditis is a common cause of hypothyroidism, with a reported preva-lence of 1-4% in the general population (6, 7).

A familial aggregation of autoimmune thy-roiditis has been described and the positivi-ty of anti-TPO antibodies has been reported in 27-34% of the relatives of patients with autoimmune thyroiditis. In addition a pa-rental history of hypo or hyperthyroidism has been reported in about 20% of mothers of subjects with HT (6).

Various studies have shown an increased prevalence of HT in first and second degree relatives of SLE patients (3,4); aim of the present study was to test the hypothesis as to whether relatives of patients with SLE and HT could be at increased risk of devel-oping HT and should therefore be screened for such condition.

A diagnosis of HT was reported in 22% of first and second-degree relatives of SLE patients with HT. However, these data may underestimate the real prevalence of HT as it could be reasonable to consider the

ge-neric hypothyroidism reported in 20 rela-tives as possible cases of HT.

Secondly, relatives were not re-evaluated and this could determine an additional

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(2)

204 Reumatismo 4/2013

L. Carli, C. Tani, S. Vagnani et al. letter to

the editor

underestimation of the real prevalence of thyroid disorders in the families of SLE pa-tients with HT.

To our knowledge this is the first study as-sessing the risk of HT among relatives of SLE patients with HT. Based on these re-sults, it might be interesting to perform ad-ditional studies on larger populations, with a direct evaluation of relatives; this could help in further clarifying if relatives of SLE patients with HT should be counseled to evaluate the presence of autoimmune thy-roid diseases.

n RefeRences

1. Pyne D, Isenberg DA. Autoimmune thyroid disease in systemic lupus erythematosus. Ann Rheum Dis. 2002; 61: 70-2.

2. Antonelli A, Fallahi P, Mosca M, Ferrari SM, Ruffilli I, Corti A, et al. Prevalence of thyroid dysfunctions in systemic lupus erythematosus. Metabolism. 2010; 59: 896-900.

3. Mosca M, Carli L, d’Ascanio A, Tani C, Ta-larico R, Baldini C, et al. Occurrence of organ-specific and systemic autoimmune diseases among the first- and second-degree relatives of Caucasian patients with connective tis-sue diseases: report of data obtained through direct patients interviews. Clin Rheumatol. 2008; 27: 1045-48.

4. Alarçon-Segovia D, Alarçon-Riquelme ME, Cardiel MH, Caeiro F, Massardo L, Villa AR, et al. Familial aggregation of systemic lupus erythematosus, rheumatoid arthritis and other autoimmune diseases in 1177 lupus patients from the GLADEL cohort. Arthritis Rheum. 2005; 52: 1138-47.

5. Boelaert K, Newby PR, Simmonds MJ, Hold-er RL, Carr-Smith JD, Heward JM, et al. Prev-alence and relative risk of other autoimmune diseases in subjects with autoimmune thyroid disease. Am J Med. 2010; 123: 183.e1-e9. 6. Marwaha RK, Sen S, Tandon N, Sahoo M,

Walia RP, Singh S, et al. Familial aggrega-tion of autoimmune thyroiditis in first-degree relatives of patients with juvenile autoimmune thyroid disease. Thyroid. 2003; 13: 297-300. 7. Roberts CGP, Ladenson PW. Hypothyroidism.

Lancet. 20004; 363: 793-803.

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