Serum neurofilament light chain - A potential biomarker for polyneuropathy in type 2 diabetes?

被引:6
|
作者
Maatta, Laura L. [1 ,2 ]
Andersen, Signe T. [1 ,2 ]
Parkner, Tina [3 ]
Hviid, Claus V. B. [3 ,4 ]
Bjerg, Lasse [2 ,5 ]
Kural, Mustafa A. [6 ]
Charles, Morten [2 ,5 ]
Sondergaard, Esben [2 ]
Sandbaek, Annelli [2 ,5 ]
Tankisi, Hatice [6 ]
Witte, Daniel R. [2 ,5 ]
Jensen, Troels S. [1 ]
机构
[1] Aarhus Univ, Danish Pain Res Ctr, Dept Clin Med, Palle Juul Jensens Blvd 165, DK-8200 Aarhus, Denmark
[2] Aarhus Univ Hosp, Steno Diabet Ctr Aarhus, Palle Juul-Jensens Blvd 11, DK-8200 Aarhus, Denmark
[3] Aarhus Univ Hosp, Dept Clin Biochem, Palle Juul Jensens Blvd 99, DK-8200 Aarhus, Denmark
[4] Aalborg Univ Hosp, Dept Clin Biochem, Hobrovej 18-22, DK-9000 Aalborg, Denmark
[5] Aarhus Univ, Dept Publ Hlth, Bartholins Alle 2, DK-8000 Aarhus, Denmark
[6] Aarhus Univ Hosp, Dept Clin Neurophysiol, Palle Juul Jensens Blvd 165, DK-8200 Aarhus, Denmark
基金
英国医学研究理事会;
关键词
Biomarkers; Diabetic complications; Diabetic polyneuropathy; Neurofilaments; Type; 2; diabetes; INTENSIVE MULTIFACTORIAL THERAPY; DIAGNOSTIC-CRITERIA; ADDITION-EUROPE; NEUROPATHY; INDIVIDUALS; VALIDATION; SEVERITY; OUTCOMES; PEOPLE; UPDATE;
D O I
10.1016/j.diabres.2023.110988
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: To investigate the relationship between neurofilament light chain (NfL) and the presence and severity of diabetic polyneuropathy (DPN).Methods: We performed cross-sectional analysis of data from 178 participants of the ADDITION-Denmark cohort of people with screen-detected type 2 diabetes and 32 healthy controls. Biobank serum samples were analyzed for NfL using single-molecule array. DPN was defined by Toronto criteria for confirmed DPN. Original and axonal nerve conduction study (NCS) sum z-scores were used as indicators of the severity of DPN and peripheral nerve damage.Results: 39 (21.9%) participants had DPN. Serum NfL (s-NfL) was significantly higher in participants with DPN (18.8 ng/L [IQR 14.4; 27.9]) than in participants without DPN (15.4 ng/L [IQR 11.7; 20.1]). There were no unadjusted s-NfL differences between controls (17.6 ng/L [IQR 12.7; 19.8]) and participants with or without DPN. Higher original and axonal NCS sum z-scores were associated with 10% higher s-NfL (10.2 and 12.1% [95% CI's 4.0; 16.8 and 6.6; 17.9] per 1 SD). The AUC of s-NfL for DPN was 0.63 (95% CI 0.52; 0.73).Conclusions: S-NfL is unlikely to be a reliable biomarker for the presence of DPN. S-NfL is however associated to the severity of the nerve damage underlying DPN.
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收藏
页数:8
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