Thyroglobulin Antibodies are Associated with Symptom Burden in Patients with Hashimoto's Thyroiditis: A Cross-Sectional Study.


Journal

Immunological investigations
ISSN: 1532-4311
Titre abrégé: Immunol Invest
Pays: England
ID NLM: 8504629

Informations de publication

Date de publication:
Feb 2019
Historique:
pubmed: 18 10 2018
medline: 21 5 2019
entrez: 18 10 2018
Statut: ppublish

Résumé

Hashimoto's thyroiditis (HT) is the most common form of autoimmune thyroid disorders characterized by lower production of thyroid hormones and positivity to autoantibodies to thyroglobulin (TgAb) and/or thyroid peroxidase (TPOAb). We performed a comprehensive phenotypic characterization of patients with HT, with specific focus on thyroid autoimmunity, to get better understanding of disease manifestation. We collected information on thyroid-specific phenotypes (TSH, T3, T4, fT4, TgAb, TPOAb, thyroid volume) and other clinical phenotypes (age, body surface area, number of hypothyroidism symptoms, blood pressure) from 290 patients with HT without levothyroxine (LT4) therapy with the aim to test for correlations between thyroid-specific and clinical phenotypes. Our key and novel finding is the existence of significant positive correlation between TgAb levels and the number of symptoms (r = 0.25, p = 0.0001) in HT patients without LT4 therapy that remained significant after adjustment for TPOAb, T3, TSH levels and thyroid volume (β = 0.66, SE = 0.3, p = 0.0299). Increased TgAb levels are significantly associated with fragile hair (p = 0.0043), face edema (p = 0.0061), edema of the eyes (p = 0.0293) and harsh voice (p = 0.0349). Elevated TgAb levels are associated with symptom burden in HT patients, suggesting a role of thyroid autoimmunity in clinical manifestations of HT. Based on these results, we recommend screening for TgAb antibodies in HT patients with symptom burden. We also suggest that further work on understandings of symptoms appearance due to their autoimmune or hypothyroid causation is needed.

Sections du résumé

BACKGROUND BACKGROUND
Hashimoto's thyroiditis (HT) is the most common form of autoimmune thyroid disorders characterized by lower production of thyroid hormones and positivity to autoantibodies to thyroglobulin (TgAb) and/or thyroid peroxidase (TPOAb). We performed a comprehensive phenotypic characterization of patients with HT, with specific focus on thyroid autoimmunity, to get better understanding of disease manifestation.
METHODS METHODS
We collected information on thyroid-specific phenotypes (TSH, T3, T4, fT4, TgAb, TPOAb, thyroid volume) and other clinical phenotypes (age, body surface area, number of hypothyroidism symptoms, blood pressure) from 290 patients with HT without levothyroxine (LT4) therapy with the aim to test for correlations between thyroid-specific and clinical phenotypes.
RESULTS RESULTS
Our key and novel finding is the existence of significant positive correlation between TgAb levels and the number of symptoms (r = 0.25, p = 0.0001) in HT patients without LT4 therapy that remained significant after adjustment for TPOAb, T3, TSH levels and thyroid volume (β = 0.66, SE = 0.3, p = 0.0299). Increased TgAb levels are significantly associated with fragile hair (p = 0.0043), face edema (p = 0.0061), edema of the eyes (p = 0.0293) and harsh voice (p = 0.0349).
CONCLUSIONS CONCLUSIONS
Elevated TgAb levels are associated with symptom burden in HT patients, suggesting a role of thyroid autoimmunity in clinical manifestations of HT. Based on these results, we recommend screening for TgAb antibodies in HT patients with symptom burden. We also suggest that further work on understandings of symptoms appearance due to their autoimmune or hypothyroid causation is needed.

Identifiants

pubmed: 30332318
doi: 10.1080/08820139.2018.1529040
doi:

Substances chimiques

Autoantibodies 0
Biomarkers 0
anti-thyroglobulin 0
Thyroglobulin 9010-34-8

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

198-209

Auteurs

Ana Barić (A)

a Department of Nuclear Medicine , University Hospital Split , Split , Croatia.

Luka Brčić (L)

b Department of Medical Biology , University of Split, School of Medicine , Split , Croatia.

Sanda Gračan (S)

a Department of Nuclear Medicine , University Hospital Split , Split , Croatia.

Veselin Škrabić (V)

c Department of Pediatrics , University Hospital Split , Split , Croatia.

Marko Brekalo (M)

a Department of Nuclear Medicine , University Hospital Split , Split , Croatia.

Marta Šimunac (M)

a Department of Nuclear Medicine , University Hospital Split , Split , Croatia.

Vesela Torlak Lovrić (VT)

a Department of Nuclear Medicine , University Hospital Split , Split , Croatia.

Iva Anić (I)

d School of Medicine , University of Split , Split , Croatia.

Maja Barbalić (M)

b Department of Medical Biology , University of Split, School of Medicine , Split , Croatia.

Tatijana Zemunik (T)

b Department of Medical Biology , University of Split, School of Medicine , Split , Croatia.

Ante Punda (A)

a Department of Nuclear Medicine , University Hospital Split , Split , Croatia.

Vesna Boraska Perica (V)

b Department of Medical Biology , University of Split, School of Medicine , Split , Croatia.

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Classifications MeSH