Yazarlar |
Burç Esra ŞAHİN
Türkiye |
Asuman Çelikbilek
Türkiye |
Yusuf Koçak
Türkiye |
Bilal İLANBEY
Kırşehir Ahi Evran Üniversitesi, Türkiye |
Dr. Öğr. Üyesi Gamze TURNA SALTOĞLU
Kırşehir Ahi Evran Üniversitesi, Türkiye |
Naime Meriç Konar
Türkiye |
Dr. Öğr. Üyesi Lokman HİZMALİ
Türkiye |
Özet |
A wide spectrum of neurological symptoms (NS) has been described in patients with COVID-19. We examined the plasma levels of neuron-specific enolase (NSE) and neurofilament light chain (NFL) together, as neuronal damage markers, and their relationships with clinical severity in patients with NS at acute COVID-19. A total of 20 healthy controls and 59 patients with confirmed COVID-19 were enrolled in this pilot prospective study. Serum NSE and NFL levels were measured by using the enzyme-linked immunoassay method from serum samples. Serum NSE levels were found to be significantly higher in the severe group than in the nonsevere group (p = 0.034). However, serum NFL levels were similar between the control and disease groups (p > 0.05). For the mild group, serum NFL levels were significantly higher in patients with the sampling time >= 5 days than in those with the sampling time <5 days (p = 0.019). However, no significant results for NSE and NFL were obtained in patients with either single or multiple NS across the groups (p > 0.05). Increased serum NSE levels were associated with disease severity regardless of accompanied NS in patients with acute COVID-19 infection. However, serum NFL levels may have a role at the subacute phase of COVID-19. |
Anahtar Kelimeler |
COVID-19 | neurofilament light chain | neurological symptoms | neuron-specific enolase | neuronal damage |
Makale Türü | Özgün Makale |
Makale Alt Türü | SSCI, AHCI, SCI, SCI-Exp dergilerinde yayımlanan tam makale |
Dergi Adı | JOURNAL OF MEDICAL VIROLOGY |
Dergi ISSN | 0146-6615 |
Dergi Tarandığı Indeksler | SCI-Expanded |
Dergi Grubu | Q1 |
Makale Dili | Türkçe |
Basım Tarihi | 01-2023 |
Cilt No | 95 |
Sayı | 1 |
Doi Numarası | 10.1002/jmv.28240 |
Makale Linki | http://dx.doi.org/10.1002/jmv.28240 |