Tomohiko Yoshida 1 , Akitoshi Nakayama 2 , Ai Tamura 3 , Seiichiro Higuchi 2 , Ikki Sakuma 2 , Hidekazu Nagano 2 , Saulo Ja Felizola 2 , Naoko Hashimoto 2 , Minoru Takemoto 1 , Ichiro Tatsuno 4 , Hisashi Koide 3 , Koutaro Yokote 3 , Tomoaki Tanaka 2 . Show Affiliations »
Abstract
CONTEXT: Hashimoto's thyroiditis is the most common cause of hypothyroidism. Patients usually respond well to oral synthetic thyroxine (levothyroxine); however, for unknown reasons some individuals present with treatment-resistant Hashimoto thyroiditis. In cases of cancer and certain infectious diseases, the ATP binding cassette (ABC) transporters have been implicated in multidrug resistance, and we hypothesized and investigated a role of ABC transporters in drug-resistant Hashimoto's thyroiditis. CASE DESCRIPTION: The patient whose case we report had a history of Hashimoto's thyroiditis, immune thrombocytopenia, and refractory hypertension, with varying treatment resistance to the oral medications prescribed for each condition. In order to establish or exclude a genetic basis for her illness, we examined the patient's gene expression profiles using peripheral blood leukocytes, and found that ABCG2/BCRPexpression was significantly high compared with healthy volunteers. Also, the increased daunomycin efflux capacity of our patient's lymphocytes was successfully inhibited by fumitremorgin C, a specific ABCG2/BCRP inhibitor, and the patient's level of thyroid-stimulating hormone increased by 248.6% after administration of intact levothyroxine tablets but decreased by 45.1% when tablets were crushed. Her average blood pressure decreased from 166.3/108.5 mmHg to 125.9/78.8 mmHg when switching from intact to crushed losartan tablets. CONCLUSIONS: High expression and accelerated efflux transporter activity of ABCG2/BCRP in the small intestine are expected to contribute to the ineffectiveness of orally administered intact tablets in cases with treatment-resistant Hashimoto's thyroiditis, and crushed tablets can be more effective for some of these patients. © Endocrine Society 2019. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
CONTEXT: Hashimoto's thyroiditis is the most common cause of hypothyroidism . Patients usually respond well to oral synthetic thyroxine (levothyroxine ); however, for unknown reasons some individuals present with treatment-resistant Hashimoto thyroiditis . In cases of cancer and certain infectious diseases , the ATP binding cassette (ABC) transporters have been implicated in multidrug resistance, and we hypothesized and investigated a role of ABC transporters in drug-resistant Hashimoto's thyroiditis . CASE DESCRIPTION: The patient whose case we report had a history of Hashimoto's thyroiditis , immune thrombocytopenia , and refractory hypertension , with varying treatment resistance to the oral medications prescribed for each condition. In order to establish or exclude a genetic basis for her illness, we examined the patient 's gene expression profiles using peripheral blood leukocytes, and found that ABCG2 /BCRPexpression was significantly high compared with healthy volunteers. Also, the increased daunomycin efflux capacity of our patient 's lymphocytes was successfully inhibited by fumitremorgin C , a specific ABCG2 /BCRP inhibitor, and the patient 's level of thyroid-stimulating hormone increased by 248.6% after administration of intact levothyroxine tablets but decreased by 45.1% when tablets were crushed. Her average blood pressure decreased from 166.3/108.5 mmHg to 125.9/78.8 mmHg when switching from intact to crushed losartan tablets. CONCLUSIONS: High expression and accelerated efflux transporter activity of ABCG2 /BCRP in the small intestine are expected to contribute to the ineffectiveness of orally administered intact tablets in cases with treatment-resistant Hashimoto's thyroiditis , and crushed tablets can be more effective for some of these patients . © Endocrine Society 2019. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
Entities: Chemical
Disease
Gene
Species
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Year: 2020
PMID: 31614366 DOI: 10.1210/clinem/dgz073
Source DB: PubMed Journal: J Clin Endocrinol Metab ISSN: 0021-972X Impact factor: 5.958