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Cognitive and Cerebrospinal Fluid Alzheimer's Disease-related Biomarker Trajectories in Older Surgical Patients and Matched Nonsurgical Controls.
Reese, Melody; Wong, Megan K; Cheong, Vanessa; Ha, Christine I; Cooter Wright, Mary; Browndyke, Jeffrey; Moretti, Eugene; Devinney, Michael J; Habib, Ashraf S; Moul, Judd W; Shaw, Leslie M; Waligorska, Teresa; Whitson, Heather E; Cohen, Harvey J; Welsh-Bohmer, Kathleen A; Plassman, Brenda L; Mathew, Joseph P; Berger, Miles.
Affiliation
  • Reese M; Department of Anesthesiology, and Center for the Study of Aging and Human Development, Duke University Medical Center, Durham, North Carolina.
  • Wong MK; Department of Anesthesiology, Duke University Medical Center, Durham, North Carolina.
  • Cheong V; Department of Anesthesiology, Duke University Medical Center, Durham, North Carolina; Duke University-National University of Singapore Medical School, Singapore.
  • Ha CI; Department of Anesthesiology, Duke University Medical Center, Durham, North Carolina.
  • Cooter Wright M; Department of Anesthesiology, Duke University Medical Center, Durham, North Carolina.
  • Browndyke J; Department of Psychiatry and Behavioral Medicine, Duke University Medical Center, Durham, North Carolina.
  • Moretti E; Department of Anesthesiology, Duke University Medical Center, Durham, North Carolina.
  • Devinney MJ; Department of Anesthesiology, Duke University Medical Center, Durham, North Carolina.
  • Habib AS; Department of Anesthesiology, Duke University Medical Center, Durham, North Carolina.
  • Moul JW; Department of Anesthesiology, and Department of Surgery, Duke University Medical Center, Durham, North Carolina.
  • Shaw LM; Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Waligorska T; Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
  • Whitson HE; Center for the Study of Aging and Human Development, Department of Medicine, and Duke/University of North Carolina Alzheimer's Disease Research Center, Duke University Medical Center, Durham, North Carolina.
  • Cohen HJ; Center for the Study of Aging and Human Development, Department of Medicine, and Duke/University of North Carolina Alzheimer's Disease Research Center, Duke University Medical Center, Durham, North Carolina.
  • Welsh-Bohmer KA; Department of Psychiatry and Behavioral Medicine, and Duke/University of North Carolina Alzheimer's Disease Research Center, Duke University Medical Center, Durham, North Carolina.
  • Plassman BL; Department of Psychiatry and Behavioral Medicine, and Duke/University of North Carolina Alzheimer's Disease Research Center, Duke University Medical Center, Durham, North Carolina.
  • Mathew JP; Department of Anesthesiology, Duke University Medical Center, Durham, North Carolina.
  • Berger M; Department of Anesthesiology, Center for the Study of Aging and Human Development, and Duke/University of North Carolina Alzheimer's Disease Research Center, Duke University Medical Center, Durham, North Carolina.
Anesthesiology ; 140(5): 963-978, 2024 May 01.
Article in En | MEDLINE | ID: mdl-38324729
ABSTRACT

BACKGROUND:

Anesthesia and/or surgery accelerate Alzheimer's disease pathology and cause memory deficits in animal models, yet there is a lack of prospective data comparing cerebrospinal fluid (CSF) Alzheimer's disease-related biomarker and cognitive trajectories in older adults who underwent surgery versus those who have not. Thus, the objective here was to better understand whether anesthesia and/or surgery contribute to cognitive decline or an acceleration of Alzheimer's disease-related pathology in older adults.

METHODS:

The authors enrolled 140 patients 60 yr or older undergoing major nonneurologic surgery and 51 nonsurgical controls via strata-based matching on age, sex, and years of education. CSF amyloid ß (Aß) 42, tau, and p-tau-181p levels and cognitive function were measured before and after surgery, and at the same time intervals in controls.

RESULTS:

The groups were well matched on 25 of 31 baseline characteristics. There was no effect of group or interaction of group by time for baseline to 24-hr or 6-week postoperative changes in CSF Aß, tau, or p-tau levels, or tau/Aß or p-tau/Aß ratios (Bonferroni P > 0.05 for all) and no difference between groups in these CSF markers at 1 yr (P > 0.05 for all). Nonsurgical controls did not differ from surgical patients in baseline cognition (mean difference, 0.19 [95% CI, -0.06 to 0.43]; P = 0.132), yet had greater cognitive decline than the surgical patients 1 yr later (ß, -0.31 [95% CI, -0.45 to -0.17]; P < 0.001) even when controlling for baseline differences between groups. However, there was no difference between nonsurgical and surgical groups in 1-yr postoperative cognitive change in models that used imputation or inverse probability weighting for cognitive data to account for loss to follow up.

CONCLUSIONS:

During a 1-yr time period, as compared to matched nonsurgical controls, the study found no evidence that older patients who underwent anesthesia and noncardiac, nonneurologic surgery had accelerated CSF Alzheimer's disease-related biomarker (tau, p-tau, and Aß) changes or greater cognitive decline.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Alzheimer Disease / Cognitive Dysfunction Type of study: Prognostic_studies Limits: Aged / Humans Language: En Journal: Anesthesiology Year: 2024 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Alzheimer Disease / Cognitive Dysfunction Type of study: Prognostic_studies Limits: Aged / Humans Language: En Journal: Anesthesiology Year: 2024 Type: Article