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Interleukin 6 (IL6) level is a biomarker for functional disease progression within IL6R 358 Ala variant groups in amyotrophic lateral sclerosis patients.
- Source :
-
Amyotrophic lateral sclerosis & frontotemporal degeneration [Amyotroph Lateral Scler Frontotemporal Degener] 2021 May; Vol. 22 (3-4), pp. 248-259. Date of Electronic Publication: 2020 Sep 14. - Publication Year :
- 2021
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Abstract
- Interleukin-6 (IL6) expression increases in atrophying muscles and lung tissue during compromised function. Considering ALS patients undergo these same pathological changes, IL6 levels may be relevant for prognostication and treatment. The amount of soluble IL6 receptor, dictated by the IL6R <superscript>358</superscript> Ala variant, and local tissue environment in which IL6 signaling occurs is known to influence the ultimate effects of IL6 in multiple diseases. In this longitudinal study, we show that serum IL6 levels negatively correlate both with the patient's functional status as measured by the overall ALSFRS-R and subscores, and with respiratory function as measured by the percent predicted FVC (ppFVC). The correlations are only present in the two-thirds of patients who carry the IL6R <superscript>358</superscript> Ala variant that mediates pro-inflammatory transsignaling in the cases of ALSFRS-R limb and respiratory subscores and ppFVC. These results suggest that some observed associations between IL6 and ALS are driven by the subset of patients carrying the IL6R <superscript>358</superscript> Ala variant and thus that any IL6-targeted therapeutic approaches may be more advantageous when aimed at this group. Specifically, with relation to respiratory decline, these patients may benefit from closer respiratory follow-up and early initiation of noninvasive ventilation.
Details
- Language :
- English
- ISSN :
- 2167-9223
- Volume :
- 22
- Issue :
- 3-4
- Database :
- MEDLINE
- Journal :
- Amyotrophic lateral sclerosis & frontotemporal degeneration
- Publication Type :
- Academic Journal
- Accession number :
- 32924606
- Full Text :
- https://doi.org/10.1080/21678421.2020.1813310