Pattern and implications of neurological examination findings in autosomal dominant Alzheimer disease.
Pattern and implications of neurological examination findings in autosomal dominant Alzheimer disease.
复制标题
常染色体显性阿尔茨海默病神经学检查结果的模式和意义。
DOI:
10.1002/alz.12684
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发表时间:
2023
期刊:
影响因子:
--
通讯作者:
Ghett
中科院分区:
文献类型:
--
作者:
Vöglein,Jonathan;Franzmeier,Nicolai;Morris,JohnC;Dieterich,Marianne;McDade,Eric;Simons,Mikael;Preische,Oliver;Hofmann,Anna;Hassenstab,Jason;Benzinger,TammieL;Fagan,Anne;Noble,JamesM;Berman,SarahB;Graff-Radford,NeillR;Ghett
IntroductionAs knowledge about neurological examination findings in autosomal dominant Alzheimer disease (ADAD) is incomplete, we aimed to determine the frequency and significance of neurological examination findings in ADAD.MethodsFrequencies of neurological examination findings were compared between symptomatic mutation carriers and non mutation carriers from the Dominantly Inherited Alzheimer Network (DIAN) to define AD neurological examination findings. AD neurological examination findings were analyzed regarding frequency, association with and predictive value regarding cognitive decline, and association with brain atrophy in symptomatic mutation carriers.ResultsAD neurological examination findings included abnormal deep tendon reflexes, gait disturbance, pathological cranial nerve examination findings, tremor, abnormal finger to nose and heel to shin testing, and compromised motor strength. The frequency of AD neurological examination findings was 65.1%. Cross‐sectionally, mutation carriers with AD neurological examination findings showed a more than two‐fold faster cognitive decline and had greater parieto‐temporal atrophy, including hippocampal atrophy. Longitudinally, AD neurological examination findings predicted a significantly greater decline over time.DiscussionADAD features a distinct pattern of neurological examination findings that is useful to estimate prognosis and may inform clinical care and therapeutic trial designs.