Plasma NfL is associated with mild cognitive decline in patients with diabetes
Plasma NfL is associated with mild cognitive decline in patients with diabetes
复制标题
血浆 NfL 与糖尿病患者轻度认知能力下降相关
DOI:
10.1111/psyg.12819
复制
发表时间:
2022
期刊:
影响因子:
2
通讯作者:
Kudo T
中科院分区:
文献类型:
--
作者:
Marutani N;Akamine S;Kanayama D;Gotoh S;Yanagida K;Maruyama R;Mori K;Miyamoto T;Adachi H;Sakagami Y;Yoshiyama K;Hotta M;Nagase A;Kozawa J;Maeda N;Otsuki M;Matsuoka T;Iwahashi H;Shimomura I;Murayama N;Watanabe H;Ikeda M;Mizuta I;Kudo T
BackgroundPatients with diabetes are at a higher risk for cognitive decline. Thus, biomarkers that can provide early and simple detection of cognitive decline are required. Neurofilament light chain (NfL) is a cytoskeletal protein that constitutes neural axons. Plasma NfL levels are elevated when neurodegeneration occurs. Here, we investigated whether plasma NfL levels were associated with cognitive decline in patients with type 2 diabetes.MethodThis study included 183 patients with type 2 diabetes who visited Osaka University Hospital. All participants were tested for cognitive function using the Mini‐Mental State Examination (MMSE) and the Rivermead Behavioural Memory Test (RBMT). NfL levels were analysed in the plasma and the relationship between NfL and cognitive function was examined.ResultsLower RBMT‐standardized profile scores (SPS) or MMSE scores correlated with higher plasma NfL levels (one‐way analysis of variance: MMSE,P= 0.0237; RBMT‐SPS,P= 0.0001). Furthermore, plasma NfL levels (β = −0.34,P= 0.0005) and age (β = −0.19,P= 0.016) were significantly associated with the RBMT score after multivariable regression adjustment.ConclusionsPlasma NfL levels were correlated with mild cognitive decline which is detected by the RBMT but not the MMSE in patients with type 2 diabetes. This suggests that plasma NfL levels may provide a valuable clinical tool for identifying mild cognitive decline in patients with diabetes.
登录
查看更多内容
影响因子:
29
作者:
Zetterberg H;Skillbäck T;Mattsson N;Trojanowski JQ;Portelius E;Shaw LM;Weiner MW;Blennow K;Alzheimer’s Disease Neuroimaging Initiative
通讯作者:
Alzheimer’s Disease Neuroimaging Initiative
影响因子:
11.2
作者:
Scherling, Carole S.;Hall, Tracey;Berisha, Flora;Klepac, Kristen;Karydas, Anna;Coppola, Giovanni;Kramer, Joel H.;Rabinovici, Gil;Ahlijanian, Michael;Miller, Bruce L.;Seeley, William;Grinberg, Lea T.;Rosen, Howard;Meredith, Jere, Jr.;Boxer, Adam L.
通讯作者:
Boxer, Adam L.
影响因子:
11.1
作者:
Mattsson N;Insel PS;Palmqvist S;Portelius E;Zetterberg H;Weiner M;Blennow K;Hansson O;Alzheimer's Disease Neuroimaging Initiative
通讯作者:
Alzheimer's Disease Neuroimaging Initiative
影响因子:
2.6
作者:
E. Laukka;Sari Jones;B. Small;L. Fratiglioni;L. Bäckman
通讯作者:
L. Bäckman
影响因子:
9.9
作者:
Weston PSJ;Poole T;Ryan NS;Nair A;Liang Y;Macpherson K;Druyeh R;Malone IB;Ahsan RL;Pemberton H;Klimova J;Mead S;Blennow K;Rossor MN;Schott JM;Zetterberg H;Fox NC
通讯作者:
Fox NC