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Generation of a Mouse Spontaneous Autoimmune Thyroiditis Model
Published on: March 17, 2023
Coexistent findings of renal glomerular disease with Hashimoto's thyroiditis
Gülay Koçak1, Bülent Huddam, Alper Azak
1Department of Nephrology, Ankara Education and Research Hospital, Ankara, Turkey. gulaykad@hotmail.com
Insights
Hashimoto's thyroiditis (HT) is linked to various glomerular diseases, with membranous glomerulonephritis (MGN) and focal segmental glomerulosclerosis (FSGS) being most common. Renal involvement in HT does not correlate with thyroid hormone levels.
Area of Science:
- Nephrology
- Endocrinology
- Autoimmune Diseases
Background:
- Hashimoto's thyroiditis (HT) is a prevalent autoimmune thyroid condition with a higher incidence in females.
- Renal involvement is a recognized, though not uncommon, complication of HT.
Purpose of the Study:
- To determine the frequency and characteristics of glomerular diseases in patients with HT.
- To explore potential shared pathogenic mechanisms between HT and glomerular diseases.
Main Methods:
- Retrospective review of 28 HT patients with renal issues (hematuria, proteinuria, renal impairment) from 2007-2011.
- Standard laboratory tests, 24-hour urine protein analysis.
- Renal biopsies in 20 patients analyzed via light microscopy and immunofluorescence.
Main Results:
- Identified FSGS (4), MGN (4), MCD (2), IgAN (3), CGN (3), and amyloidosis (1).
- Three biopsies showed nonspecific findings.
- Urinary protein excretion and GFR were not associated with thyroid hormone or autoantibody levels.
Conclusions:
- Glomerular pathologies in HT patients mirror those in the general population.
- Membranous glomerulonephritis (MGN), focal segmental glomerulosclerosis (FSGS), and IgA nephritis (IgAN) are the most frequent glomerular lesions observed in HT.
Aim And Background:
Hashimoto's thyroiditis (HT) is a common autoimmune thyroid disease with a female preponderance. Renal involvement in HT is not uncommon. In the present study, we aimed to define the frequency and characteristics of the glomerular diseases associated with HT and further the understanding of any common pathogenesis between HT and glomerular disease.
Materials And Methods:
We reviewed retrospectively 28 patients with HT who were referred to our Department because of unexplained haematuria, proteinuria or renal impairment from 2007 to 2011. Routine laboratory investigations including blood count, serum biochemistry, urinalysis and 24-h urinary protein excretion were performed on all patients. Renal biopsy was performed in 20 patients with HT, and the specimens were examined by light microscopy and immunofluorescence staining.
Results:
We detected four cases of focal segmental glomerulosclerosis (FSGS), four membranous glomerulonephritis (MGN), two minimal-change disease (MCD), three immunoglobulin A nephritis (IgAN), three chronic glomerulonephritis (CGN) and one amyloidosis. In three patients, the renal biopsy findings were nonspecific. Daily urinary protein excretion and glomerular filtration rates were found to be independent of the level of thyroid hormone and thyroid-specific autoantibodies.
Conclusion:
Glomerular pathologies associated with HT are similar to those in the general population, the most common lesions being MGN, FSGS and IgA nephritis.
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