- Open Access
Sex and genetic differences in postoperative cognitive dysfunction: a longitudinal cohort analysis
Biology of Sex Differences volume 10, Article number: 14 (2019)
Postoperative cognitive dysfunction (POCD) is a common postoperative complication experienced by patients aged 65 years and older, and these older adults comprise more than one third of the surgical patients in the USA. Because not everyone with a history of exposure to surgery and anesthesia develops POCD, there are likely major biological risk factors involved. There are important gaps in our knowledge regarding whether genetic makeup, biological sex, or other Alzheimer’s disease risk factors predispose older adults to developing POCD. We set out to determine whether biological sex and Apolipoprotein E-ε4 (APOE4) carrier status increase the risk of developing POCD in older adults.
We performed a cohort analysis of 1033 participants of prospective longitudinal aging studies. Participants underwent regular cognitive test batteries and we compared the annual rate of change over time in various cognitive measures in the women exposed to surgery and general anesthesia compared to the men exposed to surgery and general anesthesia. Mixed-effects statistical models were used to assess the relationship between biological sex, APOE4 carrier status, surgery and anesthesia exposure, and the rate of change in cognitive test scores.
When comparing all men (n = 89) and women (n = 164) who had surgery, there were no significant sex differences in postoperative cognitive outcomes. However, men with an APOE4 allele performed significantly worse on cognitive testing following surgery and anesthesia than women APOE4 carriers, even after adjusting for age, education level, and comorbidities.
Older men with APOE4 allele may be more vulnerable to postoperative cognitive dysfunction than older women with APOE4 allele.
Adults 65 years and older represent the fastest-growing age group in the USA and account for one third of all surgical patients. These older adults are at the highest risk for deleterious perioperative neurocognitive disorders (PND) such as postoperative delirium and postoperative cognitive dysfunction (POCD). Postoperative delirium occurs in up to 65% of older adults and is characterized by inattention and confusion . POCD, occurring in up to 40% of older surgical patients , is a syndrome characterized by an objective decline in cognition postoperatively when compared to preoperative function as measured by a decrease in performance on a neuropsychological test battery. POCD is independently associated with increased mortality, length of hospitalization, healthcare costs, early departure from the workforce, and overall decreased quality of life [2, 3]. Although postoperative delirium and POCD are separate entities, it is possible that they are interrelated. Studies show that patients who experience postoperative delirium are at increased risk for POCD and are even at a greater risk of progression to dementia [4, 5]. However, because not every older adult exposed to surgery and anesthesia develops PND, there are likely biological risk factors involved. While there is considerable evidence to support age, education level, and preexisting cognitive dysfunction as risk factors for PND, it is currently unclear whether the interaction of biological sex or genetic risk factors with exposure to surgery and anesthesia leads to either postoperative delirium or POCD .
Several recent large epidemiologic studies found that anesthesia and surgery not only lead to postoperative cognitive dysfunction (POCD) but also increase the Alzheimer’s disease (AD) risk [1, 7]. Similarly, a prospective longitudinal study of older men and women undergoing cardiac surgery found that the prevalence of dementia 7.5 years after cardiac surgery was greatly increased compared to population prevalence . Human biomarker investigations reveal that ratios of phosphorylated tau:amyloid beta (Aβ) in the cerebrospinal fluid convert to an AD pattern postoperatively [5, 8] and that surgical patients have increased rates of brain atrophy compared to controls [9, 10]. Further, animal studies indicate that surgery and anesthesia contribute to cognitive decline and AD-associated neuropathologic changes including neuroinflammation, Aβ aggregation, and tau hyperphosphorylation [8, 11,12,13,14,15].
It is well established that the gene most strongly associated with AD is apolipoprotein E (APOE). However, to date, there are conflicting reports in the literature regarding whether the presence of an APOE4 allele confers a higher risk for developing postoperative cognitive dysfunction (POCD) . Further, it is known that the APOE4 allele confers an increased risk of AD in a sex-dependent manner, disproportionately affecting women in both prevalence and severity ; almost 2/3 of American seniors living with AD are women. On the other hand, several studies have shown that older men are more likely to develop postoperative delirium when compared to older women [18,19,20].
In order to begin to elucidate the role of genetic factors and biological sex in the development of POCD, we investigated the associations of sex, APOE4 carrier status, and exposure to surgery/general anesthesia (GA) with postoperative cognitive decline in 1033 participants from several prospective longitudinal cohort studies of the Oregon Alzheimer’s Disease Center (OADC). We hypothesized that APOE4+ women and APOE4+ men exposed to surgery and general anesthesia would experience different rates of postoperative cognitive decline.
Database sources and study population
We performed a retrospective cohort analysis of 1033 subjects who participated in a number of Oregon Alzheimer’s disease Center (OADC) longitudinal cohort studies: the Oregon Brain Aging Study (OBAS) (n = 297) [21, 22], the Intelligent Systems for Assessment of Aging Changes (ISAAC) Study (n = 116) , the Klamath Exceptional Aging Project (KEAP) (n = 175) [24, 25], the African American Dementia and Aging Project (AADAPt) (n = 54), the Oregon Community Brain Donor Program (CBDP) (n = 97), the Oregon Living Laboratory (OLL) (n = 59), and the Layton Alzheimer’s Disease Center patient registry (n = 235). All studies were approved by the Oregon Health & Science University’s institutional review board, and all participants provided written informed consent. Using the above cohorts, we derived a comprehensive longitudinal dataset including demographic background, known APOE status, (determined via restriction digest, sequencing a PCR product, or by SNP genotyping) and cognitive decline. In order to appropriately contribute to the longitudinal analyses, all participants were required to have at least one follow-up visit during their study involvement for inclusion into the present cohort. At time zero (study enrollment), all participants began in the non-surgical group. Participants were then assigned to the surgical group upon undergoing surgery/GA. We compared the rate of change over time in various cognitive measures (Table 1). Participants underwent cognitive test batteries annually.
Dementia assessments included the Mini-Mental State Examination (MMSE), Clinical Dementia Rating (CDR), and CDR sum of boxes. The battery of tests used in the neuropsychological analysis, which have been described previously , assessed multiple cognitive domains and included Animal Category Fluency and Trail Making Test B for executive function, the Symbol Digit Modalities Test (SDMT) and Digit Symbol Test for attention and concentration, and Logical Memory Delayed Recall and Consortium to Establish a Registry for AD (CERAD) Word List Delayed Recall for memory. The cognitive tests administered are standard, validated measures commonly used in longitudinal aging and dementia studies. The Clinical Dementia Rating is a scale used to stage dementia based on six domains of Memory, Orientation, Judgment and Problem-solving, Community Affairs, Home and Hobbies, and Personal Care. Each domain is rated on a five-point scale. The CDR sum of boxes is the total sum of these six points . Mini-Mental State Examination (MMSE) is a 30-point questionnaire used to measure cognitive impairment and screen for dementia . Animal Fluency is the number of animals a subject can name in 1 min . Trail Making Test Part B requires the subject to draw lines between alternating numbers and letters in sequence as fast as they can. The score is the number of seconds to complete the test up to a maximum of 300 s . Symbol Digit Modalities Test (SDMT) asks subjects to substitute numbers for corresponding symbols. Digit Symbol Test asks subjects to follow a key and draw the symbol that belongs with each number displayed in a series of rows. The score is the number of correct symbols drawn in 90 s . Logical Memory Delayed Recall is a story memory test with a 20–30 min delay . CERAD Word List Delayed Recall is a memory test. Ten words are presented and the subject is asked to recall the words again after a delay with distraction .
Mixed-effects longitudinal regression was used to assess the influence of exposure to surgery/GA on the longitudinal change of the previously described response variables and how those alterations contrasted according to sex and APOE4 carrier status. Main effects of surgery, sex, and APOE4 carrier status on rates of change were first considered for subjects before assessment of the interactions between those key study covariates. Confounders previously identified as influences on the outcomes were selected a priori (age, education level, Cumulative Illness Rating Score (CIRS) at baseline) and were controlled for in all regression models; additionally, baseline values of outcomes were also controlled for when directly assessing rates of change. The Cumulative Illness Rating Score (CIRS) is a validated and reliable method to measure comorbidity previously cited as a key source of variance when evaluating these cohorts [33,34,35]. The key study covariates of interest, exposure to surgery/GA, APOE4 status, and sex, were dichotomized to give four groups for each sex (Surgery-exposed APOE4 carriers, unexposed APOE4 carriers, exposed non-carriers, and unexposed non-carriers). Differences in the longitudinal rates of change were then directly contrasted between the groups using the appropriate design matrices to identify the corresponding effects of sex, genotype, and surgical exposure.
Carrier status of the APOE4 allele pooled both heterozygous (APOE2,4 and APOE3,4) and homozygous (APOE4,4) carriers into a single APOE4+ group to create the dichotomous variable of APOE4 carriers vs non-carriers. This was done due to the limited number of APOE2,4 carriers and homozygous APOE4,4 carriers as to avoid overfitting of model covariates. There were only three participants with homozygosity for E4 with surgical exposure; two men and one woman. In addition, no difference in homozygous vs heterozygous carriers was observed with respect to either sex or surgical exposure.
With multiple distinct longitudinal cohorts used in this study (i.e. OBAS, ISAAC, etc.), the annual rates of change in outcomes were contrasted among the different studies to evaluate any potential cohort dependencies. Cohort-based population differences were observed in the response at entry into the studies but had no influence on rates of change, the principal consideration of the current study, and were therefore considered differences in natural history for the subjects. With no observable difference in the time-dependent changes in outcomes between the study populations, the multiple cohorts were pooled into a single disposition.
A mixed-effects model framework was used to most appropriately leverage the repeated visits within the studies and correct for serial correlation according to subject. A compound symmetry error covariance model was used with parameters estimated using restricted maximum likelihood procedures with missing data points in the analytical sample considered missing at random. Model diagnostics used a combination of formal fit criteria, specifically Cook’s distance and the observation leverages, and visual inspection of the residual plots to evaluate model fit and integrity. Individual data points within subjects found to be both outcome outliers as well as having undue and extensive influence on sensitivity of longitudinal change were removed from the final analysis and prevent false significance. Removal of these overly influential observations were specifically done for MMSE (2 observations: scores of 6 and 2 at study exit), CDR-SB (1 observation: score of 18 at study exit), Digit Symbol (3 observations: scores of 83 and 88 at study entry, score of 7 at study exit), and SDMT (1 observation: score of 1 at study exit). Due to the use of multiple outcomes, results were only considered significant at p < 0.05 after a two-level correction to the p values. Significance for a given statistic was required to first meet a false-positive rate of α = 0.05 while maintaining 80% discriminative power. The significance of this selected set was then further adjusted using the more stringent Holm-Sidak family-wise error rate (FWER) correction to correct for multiple comparisons. Final significance of a given model was based on these FWER adjusted p values. A three-way interaction between sex, APOE4 status, and anesthesia exposure was the main variable used to evaluate any longitudinal contrasts between subject sex, genetic factors and surgical/general anesthetic exposure and identify final moderating effects among the three covariates of interest.
Out of a total of 1033 participants with known APOE status, there were 382 men and 651 women while 253 participants had surgery/GA after study enrollment (men n = 89, women n = 164). The mean follow-up after study enrollment was 7.3 years (SD = 4.7), and the mean follow-up after surgery/GA was 6.3 years (SD = 4.3). Demographics, past medical history characteristics, and cognitive outcomes at study entry for all participants are listed in Table 2 along with differences according to sex. For the entire cohort, including all participants regardless of surgical exposure status, women entered the studies older (81.0 vs 78.4 years, p < 0.001) while the men were significantly more educated (15.0 vs 13.9 years, p < 0.0001) and had an increased prevalence of obesity (63% vs 29%, p < 0.0001). Overall, men were more likely to be APOE4 carriers (35% vs 28% p = 0.008) although this sex disparity was not observed for subjects with eventual exposure to surgery/GA (p = 0.76). The analytic cohort was 86% white and 14% non-white (Black, Asian, or Native American). There was no difference in APOE4 carrier prevalence in non-white compared to white participants (32% vs 20%, p = 0.27). With regard to participant comorbidities, there was no difference in average CIRS score nor prevalence of diabetes between the two sexes. There was, however, an increased prevalence of hypertension (74% vs 52%, p < 0.001) and thyroid disorders (11 vs 2%, p < 0.01) in the women exposed to surgery/GA when compared to men. Cognitive outcomes saw some sex distinctions at study entry with women showing better performance on MMSE (25.8 vs 26.7, p = 0.008), the CERAD delayed word list (5.4 vs 6.0, p = 0.002), and Digit Symbol test (34.9 vs 38.6, p = 0.003) while men exhibited better baseline performance on Animal Category Fluency (17.8 vs 16.3, p < 0.001).
No sex differences in postoperative cognitive decline after exposure to surgery & general anesthesia
After controlling for age, level of education, APOE4, Cumulative Illness Rating Scale (CIRS) score, and baseline outcome values, there were many outcomes with altered rates of change after surgical exposure when pooling men and women together and comparing all exposed participants to all unexposed participants (Table 3, surgical exposure main effect). However, there were no sex differences in rate of postoperative cognitive decline after exposure to surgery/GA on any of the specific tests (Table 3, sex effect-surgical exposure). Further, there were no sex differences in the rate of decline in cognitive test scores when comparing men and women who were not exposed to surgery/GA (Table 3, sex effect-no surgical exposure).
Older men with APOE4+ are at higher risk of postoperative cognitive dysfunction
Next, we divided the above cohort by APOE4 carrier status, and repeated the analyses comparing the associations of surgery/GA exposure and sex within the same APOE4 carrier to identify the difference in sex-exposure effects with respect to carrier status. The only outcome revealing a sex difference among APOE4 non-carriers in rate of decline was CDR-SB: APOE4− women declined more rapidly after surgery in CDR-SB than APOE4− men (Table 4). For all other outcomes analyzed, there was no interaction between sex and surgical exposure for APOE4 non-carriers. However, when we examined the sex-exposure interaction for APOE4+ carriers, we found that men with at least one copy of the APOE4 allele who were exposed to surgery/GA had a more rapid rate of decline in tests of global cognitive function (MMSE and CDR-SB) and memory (Logical Memory, CERAD word list) (Fig. 1 and Table 5). There were no significant differences in decline on tests of attention or executive function between the two groups. (Tables 4 and 5).
Because not every older adult develops POCD following surgery and anesthesia, we explored whether biological risk factors were involved. Our findings demonstrated novel sex-APOE4 allele interactions for postoperative cognitive decline. Similar to previous reports, we found that men and women had similar rates of postoperative cognitive decline [36,37,38]. However, sex differences emerged with stratified analyses, comparing women and men with the same APOE4 carrier status. Men with an APOE4 allele had more severe postoperative cognitive decline compared to women with an APOE4 allele. These findings suggest a potential explanation for the discordance in the literature regarding the relationship between postoperative cognitive decline and the APOE4 allele .
There has been increasing evidence that the presence of an APOE4 allele confers disease risk in a sex-dependent manner. Studies have shown that APOE4 confers a greater AD risk in women compared to men . Women with APOE4 also have an excess of AD pathology, including neuritic plaques and neurofibrillary tangles [39, 40]. Furthermore, at advanced ages such as those under study in this cohort, a much greater proportion of women are demented compared to men. We speculate that these factors create a “ceiling effect” in women such that the effects of additional brain insults in APOE4 females are not very potent, whereas in men there is more potential for surgery/GA to result in an increase in dementia. Additionally, there is complexity to the relationship between sex and APOE4 carrier status. It has also been demonstrated that men who were APOE4 carriers diagnosed with mild cognitive impairment (MCI) or AD have higher risks of brain microbleeds compared to APOE4-carrying women with MCI or AD .
The novel sex-APOE4 allele interactions for postoperative cognitive decline suggest that APOE4 carrier status may play an essential role in the male excess of postoperative delirium. While several studies have shown greater postoperative delirium among men [18,19,20], to date there are no investigations revealing a sex difference in postoperative cognitive dysfunction, though none of these investigations have assessed sex-APOE4 interactions. Future studies could consider sex-genetic risk factor interactions in the incidence of deleterious postoperative neurocognitive outcomes, such as delirium and POCD.
Building knowledge regarding the potential impact of sex and APOE4 genotype in older adults facing decisions regarding surgery is important for several reasons. First, if health care providers knew who was at a higher risk for postoperative cognitive decline, they would be able to more accurately counsel these individuals and their families regarding surgical risks and benefits, potentially leading to a decision to forego an elective surgical procedure. Second, this information would also inform key postoperative care and appropriate discharge planning. Many studies have shown that multidisciplinary proactive, personalized discharge planning contributes to increased patient satisfaction, decreased hospital length of stay, and reduced readmission to the hospital [42, 43].
One limitation of this investigation is that the surgical and anesthetic history was obtained by self-report from participants and/or caregivers. However, participants are interviewed twice annually in an attempt to accurately capture this type of health information, increasing confidence in this data. Because we do not have access to surgical or anesthetic records and are unable to account for potentially important differences including duration of general anesthesia, specific anesthetic agents used, or perioperative complications. Another limitation of this and other POCD studies is that participants undergoing surgery and anesthesia might have fundamental differences compared to those who did not have a surgical exposure. We did adjust for age, education level, and CIRS in our data analyses in an attempt to decrease this confounder. Finally, we note that although we had 1069 total participants in this study, only 57 participants that were exposed to surgery/GA were APOE4+. Despite this small number, we were still adequately powered to determine a significant rate of cognitive decline between groups.
Using a retrospective analysis of multiple prospective, longitudinal aging studies, OBAS, ISAAC, KEAP, AADAPt, CBDP, OLL, and the Layton Alzheimer’s Disease Center patient registry, we have shown that APOE4+ men have an increased rate of decline in cognition after exposure to surgery and anesthesia than women APOE4 carriers. This study builds upon prior research indicating that APOE4 has sex-based health implications that may affect treatments. This study is an important initial step to begin to elucidate the role of sex and genetic variables on postoperative outcomes. Moving forward, researchers should consider testing for the effects of genes implicated in postoperative cognitive decline by sex, rather than combing data for both sexes. These investigations are necessary to move toward personalized strategies to improve postoperative outcomes in older adults.
African American Dementia and Aging Project
- APOE :
Oregon Community Brain Donor Program
Clinical Dementia Rating
Clinical Dementia Rating sum of boxes
Consortium to Establish a Registry for Alzheimer’s Disease
Cumulative Illness Rating Score
Family-wise error rate
Intelligent Systems for Assessment of Aging Changes
Klamath Exceptional Aging Project
Mild cognitive impairment
Mini-Mental State Examination
Oregon Alzheimer’s Disease Center
Oregon Brain Aging Study
Oregon Living Laboratory
Postoperative cognitive dysfunction
Symbol Digit Modalities Test
Chen PL, et al. Risk of dementia after anaesthesia and surgery. Br J Psychiatry J Ment Sci. 2014;204(3):188–93.
Monk TG, et al. Predictors of cognitive dysfunction after major noncardiac surgery. Anesthesiology. 2008;108(1):18–30.
Steinmetz J, et al. Long-term consequences of postoperative cognitive dysfunction. Anesthesiology. 2009;110(3):548–55.
Evered LA, et al. Prevalence of dementia 7.5 years after coronary artery bypass graft surgery. Anesthesiology. 2016;125(1):62–71.
Palotas A, et al. Coronary artery bypass surgery provokes Alzheimer’s disease-like changes in the cerebrospinal fluid. J Alzheimers Dis. 2010;21(4):1153–64.
Hogan KJ. Hereditary vulnerabilities to post-operative cognitive dysfunction and dementia. Prog Neuro-Psychopharmacol Biol Psychiatry. 2013;47:128–34.
Chen CW, et al. Increased risk of dementia in people with previous exposure to general anesthesia: a nationwide population-based case-control study. Alzheimers Dement. 2014;10(2):196–204.
Tang JX, et al. Human Alzheimer and inflammation biomarkers after anesthesia and surgery. Anesthesiology. 2011;115(4):727–32.
Kline RP, et al. Surgery and brain atrophy in cognitively normal elderly subjects and subjects diagnosed with mild cognitive impairment. Anesthesiology. 2012;116(3):603–12.
Schenning KJ, et al. Surgery is associated with ventricular enlargement as well as cognitive and functional decline. Alzheimers Dement. 2016;12(5):590–7.
Xie Z, et al. The inhalation anesthetic isoflurane induces a vicious cycle of apoptosis and amyloid beta-protein accumulation. J Neurosci. 2007;27(6):1247–54.
Planel E, et al. Anesthesia leads to tau hyperphosphorylation through inhibition of phosphatase activity by hypothermia. J Neurosci. 2007;27(12):3090–7.
Fodale V, et al. Anaesthetics and postoperative cognitive dysfunction: a pathological mechanism mimicking Alzheimer’s disease. Anaesthesia. 2010;65(4):388–95.
Liu H, Weng H. Up-regulation of Alzheimer’s disease-associated proteins may cause enflurane anesthesia induced cognitive decline in aged rats. Neurol Sci. 2014;35(2):185–9.
Xu Z, et al. Age-dependent postoperative cognitive impairment and Alzheimer-related neuropathology in mice. Sci Rep. 2014;4:3766.
Cao L, et al. Association between APOE epsilon 4 allele and postoperative cognitive dysfunction: a meta-analysis. Int J Neurosci. 2014;124(7):478–85.
Altmann A, et al. Sex modifies the APOE-related risk of developing Alzheimer disease. Ann Neurol. 2014;75(4):563–73.
Oh ES, et al. Sex differences in hip fracture surgery: preoperative risk factors for delirium and postoperative outcomes. J Am Geriatr Soc. 2016;64(8):1616–21.
Lee HB, et al. Predisposing factors for postoperative delirium after hip fracture repair in individuals with and without dementia. J Am Geriatr Soc. 2011;59(12):2306–13.
Edlund A, et al. Delirium before and after operation for femoral neck fracture. J Am Geriatr Soc. 2001;49(10):1335–40.
Howieson DB, et al. Natural history of cognitive decline in the old old. Neurology. 2003;60(9):1489–94.
Howieson DB, et al. Neurologic function in the optimally healthy oldest old. Neuropsychological evaluation. Neurology. 1993;43(10):1882–6.
Kaye JA, et al. Intelligent Systems For Assessing Aging Changes: home-based, unobtrusive, and continuous assessment of aging. J Gerontol B Psychol Sci Soc Sci. 2011;66(Suppl 1):i180–90.
Leahy MJ, Thurber D, Calvert JF Jr. Benefits and challenges of research with the oldest old for participants and nurses. Geriatr Nurs. 2005;26(1):21–8.
Goeres LM, et al. Rural-urban differences in chronic disease and drug utilization in older Oregonians. J Rural Health. 2016;32(3):269–79.
Morris JC. The Clinical Dementia Rating (CDR): current version and scoring rules. Neurology. 1993;43(11):2412–4.
Folstein MF, Folstein SE, McHugh PR. Mini-mental state. J Psychiatr Res. 1975;12(3):189–98.
Chan AS, et al. Semantic network abnormality predicts rate of cognitive decline in patients with probable Alzheimer’s disease. J Int Neuropsychol Soc. 1995;1(3):297–303.
Armitage SG. An analysis of certain psychological tests used for the evaluation of brain injury. Psychol Monogr. 1946;60(1):i-48.
Wechsler D. Manual for the Wechsler Adult Intelligence Scale—revised. San Antonio, TX: The Psychological Corporation; 1981.
Wechsler D. WMS-R: Wechsler Memory Scale-Revised: manual. San Antonio: Psychological Corporation; 1987.
Rosen WG, Mohs RC, Davis KL. A new rating scale for Alzheimer’s disease. Am J Psychiatry. 1984;141(11):1356–64.
de Groot V, et al. How to measure comorbidity. A critical review of available methods. J Clin Epidemiol. 2003;56(3):221–9.
Parmelee PA, et al. Validation of the cumulative illness rating scale in a geriatric residential population. J Am Geriatr Soc. 1995;43(2):130–7.
Linn BS, Linn MW, Gurel L. Cumulative illness rating scale. J Am Geriatr Soc. 1968;16(5):622–6.
Hogue CW, et al. Gender influence on cognitive function after cardiac operation. Ann Thorac Surg. 2003;76(4):1119–25.
Newman MF, et al. Longitudinal assessment of neurocognitive function after coronary-artery bypass surgery. N Engl J Med. 2001;344(6):395–402.
Kadoi Y, et al. Decrease in jugular venous oxygen saturation during normothermic cardiopulmonary bypass predicts short-term postoperative neurologic dysfunction in elderly patients. J Am Coll Cardiol. 2001;38(5):1450–5.
Barnes LL, et al. Sex differences in the clinical manifestations of Alzheimer disease pathology. Arch Gen Psychiatry. 2005;62(6):685–91.
Corder EH, et al. The biphasic relationship between regional brain senile plaque and neurofibrillary tangle distributions: modification by age, sex, and APOE polymorphism. Ann N Y Acad Sci. 2004;1019:24–8.
Cacciottolo M, et al. The APOE4 allele shows opposite sex bias in microbleeds and Alzheimer’s disease of humans and mice. Neurobiol Aging. 2016;37:47–57.
Harari D, et al. Proactive care of older people undergoing surgery (‘POPS’): designing, embedding, evaluating and funding a comprehensive geriatric assessment service for older elective surgical patients. Age Ageing. 2007;36(2):190–6.
Lin C-J, et al. Discharge planning. Int J Gerontol. 2012;6(4):237–40.
This study was funded in part by an Agency for Healthcare Research & Quality-funded BIRCWH K12 award (K12 HD 043488) and by grants from the National Institutes of Health (P30AG024978, R01AG024059, P30AG008017), a Merit Review Grant from the Department of Veteran’s Affairs, and an Alzheimer’s Association Clinician Scientist Fellowship.
Availability of data and materials
The datasets generated and/or analyzed during the current study are available from the corresponding author on reasonable request.
Ethics approval and consent to participate
All studies were approved by the Oregon Health & Science University’s institutional review board (IRB), and all participants provided written informed consent. Electronic IRB (eIRB) numbers are as follows: eIRB 361 Oregon Brain Aging Study (OBAS), eIRB 2353 Intelligent Systems for Assessment of Aging Changes (ISAAC), eIRB 688 Klamath Exceptional Aging, eIRB 1480 African American Dementia and Aging Project (AADAPt), eIRB 1639 Oregon Community Brain Donor Program (CBDP), eIRB 2765 Oregon Living Laboratory (OLL), eIRB 725 Layton Alzheimer’s Disease Center patient registry. Whenever possible, investigators obtained valid informed consent directly from the research participant. If the research participant lacks decision-making capacity, the investigator obtains consent from an Authorized Research Representative (ARR). If at any point the participant expresses resistance or dissent to participation or to the use of ARR consent, the participant is excluded from the research study. The participant may designate an ARR when the participant has adequate decision-making capacity to do so, or an ARR may be identified by the investigator in the same manner that a decision maker for health care treatment would be identified. An investigator still obtains assent of the participant in addition to consent from the ARR.
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Schenning, K.J., Murchison, C.F., Mattek, N.C. et al. Sex and genetic differences in postoperative cognitive dysfunction: a longitudinal cohort analysis. Biol Sex Differ 10, 14 (2019). https://0-doi-org.brum.beds.ac.uk/10.1186/s13293-019-0228-8
- Cognitive decline
- Apolipoprotein E ε4 (APOE4)
- Alzheimer’s disease
- Cohort study
- Sex influence