Gastrointestinal Biopsy Obtained During Cancer Screening, a Biological Marker for [alpha]-Synucleinopathy?

• Published in: Journal of neuropathology and experimental neurology Vol. 81; no. 5; p. 356
• Main Authors: Jotanovic, Jelena, Milin-Lazovic, Jelena, Alafuzoff, Irina
• Format: Journal Article
• Language: English
• Published: Oxford University Press 01.05.2022
• Subjects: Biopsy; Cancer; Colon cancer; Degeneration; Diagnosis; Health aspects; Immunohistochemistry; Intestine, Small; Nerve proteins; Nervous system; Physiological aspects; Sweden
• ISSN: 0022-3069
• DOI: 10.1093/jnen/nlac023

The hallmark alteration in [alpha]-synucleinopathies, [alpha]-synuclein, is observed not only in the brain but also in the peripheral tissues, particularly in the intestine. This suggests that endoscopic biopsies performed for colon cancer screening could facilitate the assessment of [alpha]-synuclein in the gastrointestinal (GI) tract. Using immunohisto-chemistry for [alpha]-synuclein, we assessed whether GI biopsies could be used to confirm an ongoing [alpha]-synucleinopathy. Seventy-four subjects with cerebral [alpha]-synucleinopathy in various Braak stages with concomitant GI biopsies were available for study. In 81% of the subjects, [alpha]-synuclein was seen in the mucosal/submucosal GI biopsies. Two subjects with severe cerebral [alpha]-synucleinopathy and a long delay between biopsy and death displayed no [alpha]-synuclein pathology in the gut, and 11 subjects with sparse cerebral [alpha]-synucleinopathy displayed GI [alpha]-synuclein up to 36 years prior to death. The finding that there was no GI [alpha]-synuclein in 19% of the subjects with cerebral [alpha]-synucleinopathy, and [alpha]-synuclein was observed in the gut of 11 subjects (15%) with sparse cerebral [alpha]-synucleinopathy even many years prior to death is unexpected and jeopardizes the use of assessment of [alpha]-synuclein in the peripheral tissue for confirmation of an ongoing cerebral [alpha]-synucleinopathy. Key Words: [alpha]-Synuclein, Biomarker, Gastrointestinal biopsy, Immunohistochemistry, Lewy body disease.