4.1 Article

Pernicious anaemia and endocrine glands antibodies

Journal

ENDOKRYNOLOGIA POLSKA
Volume 70, Issue 2, Pages 143-150

Publisher

VIA MEDICA
DOI: 10.5603/EP.a2018.0086

Keywords

pernicious anaemia; antibody; thyroid; adrenal; pituitary; Hashimoto; autoimmune disease

Funding

  1. Medical University of Silesia [KNW-1-135/N/3/0, KNW-1-056/N/4/0, KNW-1-158/K/5/0]

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Introduction: The aim of the study was to determine the frequency of occurrence of antibodies participating in the development of endocrine diseases in patients with autoimmune haematopoietic disease, thus documenting the potential suitability of specific diagnostic and screening tests. Material and methods: The study group consisted of 124 persons (men and women) with newly diagnosed pernicious anaemia (PA) and a control group (C) of 41 healthy people. Antibodies against: intrinsic factor (IFAb), gastric parietal cells (APCA), thyroid peroxidase (TPOAb), thyroglobulin (TgAb), adrenal cortex (AdrenalAb), and pituitary anterior lobe (PituitaryAb) were determined in the blood. Results: 1. The risk of the presence of antibodies against endocrine glands in patients with PA can be classified in order: TPOAb and/or TgAb-41.1%, TPOAb-36.3%, TgAb-25.0%, TPOAb and TgAb-20.2%, AdrenalAb-1.6%, PituitaryAb-0.8%. 2. TPOAb and/or TgAb (mainly TPOAb) are more frequently present in patients with PA, who have IFAb and/or APCA. This correlation is most evident in patients with simultaneous occurrence of IFAb and APCA. 3. Among patients with PA, the simultaneous presence of antibodies IFAb and/ or APCA with TPOAb and/or TgAb antibodies is most likely in women over 45 years of age. 4. In group C, 12% had at least one of two antithyroid antibodies (TgAb twice as often as TPOAb), and 2.4% had both. AdrenalAb and PituitaryAb are not found in healthy persons. Conclusions: In patients with PA, a screening for autoimmune thyroid disease is justified, which should first involve the determination of TPOAb (further TgAb) in the blood. The assessment of antithyroid antibodies should be recommended primarily to patients with PA, who have IFAb and/or APCA, and in particular those with concurrent IFAb and APCA.

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