Terminal decline in objective and self-reported measures of motor function before death: 10 year follow-up of Whitehall II cohort studyBMJ 2021; 374 doi: https://doi.org/10.1136/bmj.n1743 (Published 05 August 2021) Cite this as: BMJ 2021;374:n1743
- Benjamin Landré, postdoctoral fellow1,
- Aurore Fayosse, statistician1,
- Céline Ben Hassen, postdoctoral fellow1,
- Marcos D Machado-Fragua, postdoctoral fellow1,
- Julien Dumurgier, associate professor1 2,
- Mika Kivimaki, professor3,
- Séverine Sabia, research associate1 3,
- Archana Singh-Manoux, professor1 3
- 1Université de Paris, Inserm U1153, CRESS, Epidemiology of Ageing and Neurodegenerative diseases, Paris, France
- 2Cognitive Neurology Center, Lariboisière – Fernand Widal Hospital, AP-HP, Université de Paris, Paris, France
- 3Department of Epidemiology and Public Health, University College London, London, UK
- Correspondence to: B Landré (or @epiageing on Twitter)
- Accepted 5 July 2021
Objectives To examine multiple objective and self-reported measures of motor function for their associations with mortality.
Design Prospective cohort study.
Setting UK based Whitehall II cohort study, which recruited participants aged 35-55 years in 1985-88; motor function component was added at the 2007-09 wave.
Participants 6194 participants with motor function measures in 2007-09 (mean age 65.6, SD 5.9), 2012-13, and 2015-16.
Main outcome measures All cause mortality between 2007 and 2019 in relation to objective measures (walking speed, grip strength, and timed chair rises) and self-reported measures (physical component summary score of the SF-36 and limitations in basic and instrumental activities of daily living (ADL)) of motor function.
Results One sex specific standard deviation poorer motor function in 2007-09 (cases/total, 610/5645) was associated with an increased mortality risk of 22% (95% confidence interval 12% to 33%) for walking speed, 15% (6% to 25%) for grip strength, 14% (7% to 23%) for timed chair rises, and 17% (8% to 26%) for physical component summary score over a mean 10.6 year follow-up. Having basic/instrumental ADL limitations was associated with a 30% (7% to 58%) increased mortality risk. These associations were progressively stronger when measures were drawn from 2012-13 (mean follow-up 6.8 years) and 2015-16 (mean follow-up 3.7 years). Analysis of trajectories showed poorer motor function in decedents (n=484) than survivors (n=6194) up to 10 years before death for timed chair rises (standardised difference 0.35, 95% confidence interval 0.12 to 0.59; equivalent to a 1.2 (men) and 1.3 (women) second difference), nine years for walking speed (0.21, 0.05 to 0.36; 5.5 (men) and 5.3 (women) cm/s difference), six years for grip strength (0.10, 0.01 to 0.20; 0.9 (men) and 0.6 (women) kg difference), seven years for physical component summary score (0.15, 0.05 to 0.25; 1.2 (men) and 1.6 (women) score difference), and four years for basic/instrumental ADL limitations (prevalence difference 2%, 0% to 4%). These differences increased in the period leading to death for timed chair rises, physical component summary score, and ADL limitations.
Conclusion Motor function in early old age has a robust association with mortality, with evidence of terminal decline emerging early in measures of overall motor function (timed chair rises and physical component summary score) and late in basic/instrumental ADL limitations.
Ageing is characterised by a decline in cognitive and motor function over the adult life course,1234 along with an increase in heterogeneity of individual trajectories, partly as a result of pathological processes of age related chronic diseases.56 In the years immediately preceding death, an accelerated decline in functioning has been observed,78 referred to as “terminal decline.”7 As described in a recent review, terminal decline is observed in multiple domains, although much of the research is confined to cognitive decline.9
Better understanding of changes in functional status in the one or two years before death is useful for planning care, but it has minimal utility for identifying individuals who could benefit from clinical or behavioural interventions. Consideration of longer spans to study decline preceding death is also supported by findings showing decline in motor and cognitive function to be manifest starting in midlife.24 Furthermore, several studies have shown midlife poorer cognitive and motor function to be associated with higher mortality risk.10111213 The long term change in trajectories of functioning before death is less well characterised in relation to motor function. For cognitive function, long term trajectories are known, and change-point studies show that differences in different measures emerge up to 15 years before death.14
Change in motor function in the years before death is a dynamic process and may reflect changes over a longer period than at end of life examined in several studies.151617 To date, few studies have considered a longer follow-up. An exception is a study showing decline in walking speed starting 10 years before death.18 Some studies have used composite measures of motor function,161920 in which the role played by strength and upper and lower body function cannot be separated. A further limitation, apart from notable exceptions,15 is a lack of studies assessing both objective and self-reported measures of function. To overcome these limitations, the aim of this longitudinal cohort study was to examine multiple measures of motor function for their associations with mortality by using time-to-event analyses to capture the importance of between person differences in motor function and retrospective trajectory analyses to compare within person change in motor function over 10 years in survivors and deceased participants. Use of this twin analytical strategy allows both between person and within person differences in motor function to be examined in relation to mortality in the same study, with the second being reflected in the shape of the change in motor function leading to death.
The Whitehall II study is an ongoing prospective cohort of 10 308 British civil servants, 6895 men and 3413 women, aged 35-55 in 1985-88.21 Since baseline, follow-up clinical examinations have taken place approximately every four to five years using home based assessment for participants who choose this option and clinic based assessments (in London and major cities in the UK) for others; each wave takes approximately two years to complete. Measurement of motor function was introduced to the study at the 2007-09 clinical examination and repeated in 2012-13 and 2015-16 (flowchart in supplementary figure A). In addition to clinical examinations within the study, data over the follow-up are obtained via linkage to electronic health records of the UK National Health Service (NHS). The NHS provides most of the healthcare in the country, including inpatient and outpatient care, and record linkage is done using a unique NHS identifier held by all UK residents. Participants provided written informed consent at each wave.
Motor function (2007-09, 2012-13, and 2015-16)
Walking speed was measured over an 8 ft (2.44 m) marked course, with no obstructions for an additional 2 ft at either end. Participants wore either low heeled, close fitting footwear or walked barefoot with instructions to “walk to the other end of the course at your usual walking pace, just as if you were walking down the street to go to the shops. Walk all the way past the other end of the tape before you stop.” Three tests were conducted, and a research nurse used a stopwatch to record the time taken to complete the test; we used the mean of three trials (m/s) in the analysis. Use of a walking stick, if habitual, was allowed.
Grip strength was measured using a Smedley hand grip dynamometer. Participants were seated, elbow on the table, forearm pointing upwards, and palm of the hand facing up. The dynamometer was adjusted to suit participants’ dominant hand and they were instructed to squeeze the dynamometer as hard as possible for two seconds. Three tests were performed with a one minute rest between tests; we used the maximum of these values in the analyses.22
Timed chair rises was the time (in seconds) to stand up and sit down five times. Participants started out sitting on an armless chair with feet resting on the floor and arms folded across the chest. They were instructed to stand up and sit down five times as quickly as possible without using their arms. To retain 275 participants with data on all other measures of motor function except timed chair rises, we imputed these data by using the sex specific mean score of the bottom fifth of performance as in a previous study.23
Self-reported functioning was measured using the physical component summary score of the Short Form 36 General Health Survey (SF-36).24 A low physical component summary score indicates limitations in self-care and daily activities, experiencing severe pain, and poor general health.
Self-reported functional limitations were assessed using difficulties in basic activities of daily living (ADL) and instrumental ADL.2526 Basic ADL were assessed by questions on the following six items: dressing, walking, bathing, eating, getting in bed, and using the toilet; instrumental ADLs included difficulty in cooking, shopping for groceries, making telephone calls, taking medication, doing housework, and managing money. Impaired functional status was determined by one or more limitations on a combined basic and instrumental ADL scale.
We defined death from any cause by using mortality records drawn from the British national mortality register (NHS Central Registry) until October 2019. The tracing exercise was carried out using the NHS identification number of each participant.
Sociodemographic variables included age, sex, ethnicity (white or non-white), marital status (living with a partner or single), and occupational position at age 50 (high, intermediate, or low, reflecting income and status at work).21 Health behaviours included smoking (never smoker, ex-smoker, current smoker), alcohol consumption (no alcohol in the previous week; moderate, 1-14 units/week; high, >14 units/week), time spent in moderate and vigorous physical activity (<150 minutes per week, at least the recommended amount of physical activity), and frequency of consumption of fruits and vegetables (less than daily, at least once a day). Body mass index, estimated using height and weight (kg/m2) assessed at the clinical examination, was categorised as <20, 20-24, 25-29.9, and ≥30.
We ascertained chronic diseases by using data from multiple sources, including clinical examinations in the study and linkage to electronic health records. We used three national databases: the national hospital episode statistics (HES) database with inpatient and outpatient data; the Mental Health Services Data Set, which in addition to inpatient and outpatient data also has data on care in the community; and the cancer registry. Chronic conditions considered were diabetes (fasting glucose ≥7.0 mmol/L, reported diabetes diagnosed by a doctor, use of diabetes medication, ICD-10 (international classification of diseases, 10th revision) codes E10-E14), coronary heart disease (12 lead resting electrocardiogram, ICD-10 codes I20-I25), stroke (MONICA-Ausburg stroke questionnaire, ICD-10 codes I60-I64), cancer (cancer registry with malignant cancer, ICD-10 codes C00-C97, to include colorectal, lung, breast, prostate, smoking related, and melanoma skin cancers), dementia (ICD-10 codes F00-F03, F05.1, G30, G31), Parkinson’s disease (self-report of longstanding illness, ICD-10 code G20), chronic obstructive pulmonary disease (self-report of longstanding illness, ICD-10 codes J41-J44), depression (self-report of longstanding illness, use of antidepressants, ICD-10 codes F32-F33), and arthritis (self-report of longstanding illness, ICD-10 codes M05, M06, M15-M19). We created a multimorbidity score as the count of these chronic conditions, ranging from 0 to 9.
We standardised all continuous measures of motor function by using sex specific mean and standard deviation from baseline (2007-09). We examined the association between motor function and mortality in two ways: firstly using time-to-event analysis and then by comparison of retrospective trajectories of motor function over 10 years.
Time-to-event analysis—We used Cox proportional hazards regression to examine the association of motor function in 2007-09, 2012-13, and 2015-16 (separate models) with mortality. We used age as the time scale, left-truncated participants at age at assessment, and right-censored them at age of death or end of mortality follow-up (October 2019), whichever came first. We verified the proportional hazards assumption by plotting Schoenfeld residuals. Analyses were adjusted firstly for sociodemographic factors (sex, ethnicity, marital status, and occupational position at age 50) (model 1); additionally for health behaviours (physical activity, alcohol, tobacco, and fruit/vegetable consumption) (model 2), and then for body mass index and the multimorbidity score (model 3). Walking speed, grip strength, and SF-36 physical component summary score measures were rescaled so that hazard ratios associated with all continuous measure of motor function reflected the association with mortality for one standard deviation poorer performance. For basic/instrumental ADL limitations, the hazard ratio reflected having at least one limitation versus none.
Retrospective analysis of motor function trajectories over 10 years—We examined trajectories of motor function by using a backwards time scale such that time 0 was 31 December 2017 for survivors and date of death for participants who died between baseline (2007-09) and 31 December 2017. Deaths after this date were not considered in these analyses to restrict analyses on mortality occurring not long after the last measure of motor function. We defined retrospective trajectories by using linear mixed models for all motor function measures except basic/instrumental ADL limitations, for which we used logistic regression with generalised estimated equation and an unstructured correlation matrix. Time and time squared, and their interactions with age at time 0, sex, ethnicity, marital status, and occupation position were included in model 1; subsequent adjustment for covariates was the same as that in the fully adjusted Cox regression (model 3). Age was centred at the overall mean at time 0, and in the linear mixed models random effects for the intercept and time were used to allow for differences in motor function at the intercept (time 0) and change in motor function over time. We estimated the difference in motor function for the continuous measures and prevalence of basic/instrumental ADL limitations in survivors and decedents for each year, over the 10 years preceding end of follow-up or death, with a positive value indicating poorer motor function performance among decedents.
We used R software (version 4.0.3) for all analyses. Cox regression, linear mixed models, generalised estimated equation, and comparisons between survivors and decedents used the survival (version 3.2-7), nlme (version 3.1-149), geepack (version 1.3-2), and emmeans (version 1.5.2-1) packages, respectively. We reported estimates with 95% confidence intervals and considered two tailed P values to be significant at the 0.05 level.
In addition to considering the motor function measures separately in Cox regression in the main analyses, we did analyses including all motor function measures in the same model. Secondly, to examine the effect of missing data, we repeated the Cox regression analysis using inverse probability weighting to reflect the study population at recruitment (1985).27 This involved calculation of the probability of being included in the present study among participants who were alive by using data from baseline on sociodemographic factors and health behaviours as well as data on chronic conditions over the follow-up; then we used the inverse of these probabilities as weights in the Cox regression. Thirdly, we examined the role of chronic diseases in time-to-event analyses stratified by the status of multimorbidity at the assessment of motor function. Fourthly, we examined the possible influence of cognitive function by adding a measure of global cognition (the Mini Mental State Examination) as a covariate to the analyses. Fifthly, as basic and instrumental ADL were combined in the main analyses, we examined them separately to determine whether trends in long term terminal decline were similar in these two measures of functional limitations. Finally, in an alternative approach, we examined the association between change in motor function over the first two measures of motor function and subsequent mortality by using Cox regression and the same covariates as in the main analyses drawn from the 2012-13 assessments.
Patient and public involvement
Participants of the Whitehall II study and members of the public were not involved in setting the research question or the outcome measures; nor were they involved in developing plans for recruitment, design, or implementation of the study. We recognise the importance of public involvement in instigating change in policy and practice, but funding for these activities was not available. The principal investigators of the Whitehall II study are in the process of seeking solutions to strengthen this aspect of the study. These analyses are part of a postdoctoral fellow’s research, for which no funds were available to consult or involve the public. Therefore, participants and members of the public could not be asked to contribute to interpretation or writing up of results before submission. We are grateful to the patient reviewer who made insightful suggestions that contributed to better contextualise our findings in the discussion section. All results are disseminated to study participants via newsletters and our website, which has a participant portal (https://www.ucl.ac.uk/epidemiology-health-care/research/epidemiology-and-public-health/research/whitehall-ii/participants-area) and to a larger audience via media outreach.
Assessment of motor function was introduced to the study protocol at the 2007-09 wave of data collection when the age range of participants was 55-79 years and repeated in 2012-13 and 2015-16, leading to smaller numbers in analyses due to drop-out and mortality (supplementary figure A). The analyses of motor function trajectories were based on 6194 participants with data on at least one of three waves of motor function and the covariates. Compared with those excluded from these analyses (n=4114), participants included in the analyses were younger (44.0 v 45.6 years at recruitment in 1985-88) and were more likely to be men (72.0% (n=4459) v 59.2% (n=2436)), be white (92.5% (n=5729) v 83.9% (n=3452)), and have higher occupational position (43.2% (n=2674) v 25.1% (n=1034)).
Among the 6194 participants included in the analyses, 654 died between baseline (2007-09) and October 2019; the mean age at death was 76.8 (SD 6.2) years. Table 1 shows that participants who died were more likely to be older at baseline (mean age 69.7 v 65.1 years) and to have multimorbidity (27.2% (n=166) v 12.1% (n=610)) and poorer motor function compared with participants alive at the end of the follow-up. The motor function measures had a modest correlation with each other, ranging from 0.21 to 0.35 (see correlation matrix in supplementary table A).
We observed no sex differences in the association between measures of motor function and mortality; P values for the interaction term between sex and motor function measures ranged from 0.12 to 0.92. We therefore combined men and women in the analyses with sex specific standardisation of continuous motor function measures. Sex specific standard deviations correspond to a difference at baseline of 26.2 cm/s and 25.4 cm/s in walking speed, 8.5 kg and 6.2 kg in grip strength, 3.3 s and 3.6 s in timed chair rises, and 8.0 and 10.7 in physical component summary score among men and women respectively.
Poor performance on both objective and self-reported measures of motor function (1 SD lower performance in continuous measures and one or more limitations in basic/instrumental ADLs) was associated with higher risk of mortality (table 2) in analyses adjusted for sociodemographics (model 1) and health behaviours (model 2). This was the case for measures of motor function in 2007-09 (mean follow-up 10.6 (SD 1.8) years; mortality/total, 610/5645), in 2012-13 (mean follow-up 6.8 (1.0) years; mortality/total, 359/5083), and 2015-16 (mean follow-up 3.7 (0.6) years; mortality/total, 150/4440). Inclusion of body mass index and the multimorbidity score as covariates (model 3) attenuated associations, but poorer scores on all motor function measures remained associated with higher risk of mortality. The associations were stronger when follow-up was shorter; for example, one standard deviation slower walking speed was associated with a 22% (95% confidence interval 12% to 33%) higher risk of mortality when assessed in 2007-09 and a 49% (24% to 79%) higher risk when assessed in 2015-16.
When all motor function measures were entered simultaneously in the Cox regression (supplementary table B), only slower walking speed was associated with higher mortality risk in the fully adjusted analyses (14% (4% to 25%) for the 2007-09 measure, 26% (10% to 44%) for the 2012-13 measure, and 29% (4% to 60%) for the 2015-16 measure of walking speed). Use of inverse probability weighting to account for missing data yielded results similar to those in the main analyses (supplementary table C). The association of motor function with mortality was similar in participants with and without multimorbidity (supplementary table D). Further adjustment for cognitive function did not alter the findings (supplementary table E).
Among the 4606 participants with motor function data in 2007-09 and 2012-13, assessments (supplementary table F; mortality, 316; mean age, 68.4 (5.7) years; mean follow-up, 7.0 (1.0) years), a one standard deviation decline in motor function over time was associated with an increased risk of mortality of 18% (5% to 32%) for walking speed, 22% (4% to 42%) for grip strength, and 16% (3% to 29%) for physical component summary score but not for timed chair rises (hazard ratio 1.08, 0.97 to 1.20). Compared with those with no basic/instrumental ADL limitations at these waves (mortality/total, 202/3567), participants who developed one limitation (mortality/total, 50/406) had a 37% (0% to 87%) higher risk of mortality.
Retrospective trajectories of motor function over 10 years leading to death
A total of 484 deaths among 6194 participants were recorded between the start (2007-09 wave of data collection) and end of follow-up (31 December 2017). The end of follow-up in these analyses was earlier than in the Cox regression to restrict deaths contiguous to the last measure of motor function. Characteristics of these participants (supplementary table G) were similar to those in participants included in the time-to-event analysis.
Figure 1 shows the retrospective trajectories of motor function over the 10 years before death in decedents and before 31 December 2017 in those alive at this date; data are standardised mean scores for all measures except basic/instrumental ADLs, for which probabilities are presented in analyses adjusted for all covariates. The accompanying differences in each of the 10 years are shown adjusted for sociodemographic variables in supplementary table H and adjusted for all covariates in table 3.
In fully adjusted analyses (model 3, table 3), mean walking speed was faster in survivors than in decedents starting at nine years before death (difference in standardised walking speed 0.21 (95% confidence interval 0.05 to 0.36); equivalent to a difference of 5.5 cm/s and 5.3 cm/s in men and women respectively) and persisted to time 0. Grip strength in survivors was higher from year 6 (0.10 (0.01 to 0.20); equivalent to 0.9 (men) and 0.6 (women) kg difference) to year 3 (0.09 (0.00 to 0.18), 0.8 (men) and 0.6 (women) kg difference) before death. The shape of the overall 10 year trajectory of walking speed and grip strength (fig 1 and table 3) was similar in survivors and decedents.
Survivors had better performance than decedents on timed chair rises starting at year 10 (0.35 (0.12 to 0.59) SD; equivalent to a difference of 1.2 (men) and 1.3 (women) seconds), and this difference increased steadily with approach to time 0 (0.81 (0.61 to 1.02) SD; corresponding to 2.7 (men) and 2.9 (women) seconds). The physical component summary score was higher in survivors, indicating better motor function, starting from year 7 (0.15 (0.05 to 0.25) SD; equivalent to 1.2 (men) and 1.6 (women) score difference), and this difference increased over the period to time 0 (0.51 (0.31 to 0.70) SD; 4.1 (men) and 5.5 (women) score difference). The probability of basic/instrumental ADL limitation was lower in survivors starting from year 4 (0.02 (0.00 to 0.04)), with an increasing divergence to year 0 (0.09 (0.20 to 0.16)). Further examination of basic and instrumental limitations separately (supplementary table I) suggested that differences between survivors and decedents were due to ADL limitations. Adjustment for cognitive function did not alter the main findings (supplementary table J).
This study of repeated objective and self-reported measures of motor function spanning 10 years before death presents two key findings. Firstly, time-to-event analysis showed poorer motor function at mean age 65, 69, and 72 years to be associated with higher risk of mortality, with associations being stronger with later life measures of motor function. Secondly, trajectories of motor function over 10 years using a backwards time scale showed divergence, or terminal decline, in timed chair rises, physical component summary score (SF-36), and basic/instrumental ADL limitations starting 10, seven, and four years before death respectively. Given the definition of terminal decline as accelerated decline in functioning before death,15 or specifically divergence in trajectories of function, our results suggest important differences in terminal decline as a function of the specific measure of motor function. The difference between survivors and decedents in mean walking speed (from year 9 to year 0) and grip strength (from year 6 to year 3) did not change in the period leading to death. Differences in retrospective trajectories were greatest for timed chair rises and smallest for grip strength; increase in differences between survivors and decedents in the period leading to death was 4.7-fold in physical component summary score, 4.5-fold in basic/instrumental ADL limitations, and 2.3-fold in timed chair rises.
Use of the terminal decline framework allows better understanding of the relation between motor function and mortality owing to assessment of within person changes in motor function.152829 Time-to-event analysis identifies the relevance of specific motor function measures, and the hazard ratio estimates reflect between person rather than within person differences in motor function. The originality of our approach is the use of retrospective trajectories, anchored to the date of death, so that distance to death is the same in those who died and survivors in comparisons of motor function. Increase in heterogeneity in individual trajectories is a hallmark of ageing56; our analysis shows this heterogeneity to be meaningfully associated with mortality.
Strengths and limitations of study
This study adds to the sparse literature on terminal decline in motor function and, to our knowledge, is the first to examine terminal and age related long term trajectories of multiple measures of motor function. The main strength of the study is the use of a twin approach, with modelling of trajectories along with Cox regression. The use of multiple measures of motor function, both objective and self-reported, is a further strength. The ability to consider a range of covariates in the analysis, including health behaviours, body mass index, and several chronic diseases, ensures that results are not driven by a certain behavioural or health profile.
The study findings need to be considered in light of some limitations. Firstly, we were not able to examine trajectories of motor function separately by cause of death owing to small number of deaths in categories of major causes of death. Some evidence suggests that the pattern of terminal decline differs according to cause of death.3031 Secondly, our findings are based on participants in early old age and may not be generalisable to deaths in the ninth and 10th decades of life. Thirdly, although a wide range of chronic conditions and health behaviours were included as covariates, acute events, such as falls or hospital admissions, also probably affect motor function trajectories. Fourthly, data are based on an occupational cohort at recruitment and participants were healthier than the general population, in terms of risk factors levels and incidence of disease. However, this does not necessarily affect risk factor-disease associations.32 For example, the associations of walking speed with mortality risk factors in Whitehall II, such as smoking, obesity, hypertension, and diabetes, are comparable to those found in 21 other cohort studies,3334 and the association between cardiovascular risk factors and incidence of cardiovascular disease in the Whitehall II study is similar to that in general population studies.33 Fifthly, the ethnicity distribution in the study reflects the UK population 30 years ago, and the study lacks sufficient numbers to allow analyses in specific minority groups.
Comparison with previous studies
The overall results from time-to-event analyses in this study are consistent with the existing literature, despite differences in the manner in which motor function was considered in the analysis. A meta-analysis that compared the lowest and highest quarters of performance found grip strength (hazard ratio 1.67), walking speed (2.87), and chair rises (1.96) to be associated with higher risk of mortality.35 Most studies in the meta-analysis had a short follow-up and were based on participants older than 70 at baseline; the exception was grip strength, for which a wider range of data were available, and these studies show stronger associations with a shorter follow-up.35 Another pooled analysis of nine cohort studies (mean age of participants 73.5 years, mean follow-up 12.2 years) reported slower walking speed to be associated with increased mortality risk.36 In our study, repeat assessments of motor function show stronger associations when the follow-up was shorter, particularly for basic/instrumental ADL limitations.
The association of self-reported measures of motor function with mortality has mostly been examined using limitations in ADL in older adults, in whom it has a robust association with mortality,373839 with follow-up ranging from one to >15 years. The evidence on physical functioning scales such as the physical component summary score from SF-36 is more limited; a recent meta-analysis of four studies with a mean follow-up of 1.8 years showed better scores to be associated with lower mortality risk (odds ratio for 1 unit increase: 0.95).40 In our study, both of these self-reported measures were associated with mortality, irrespective of the age at assessment. As with the objective measures of motor function, the hazard ratios of associations with mortality were higher when self-reported function was assessed closer to death.
Studies with repeat measures of motor function have shown decline in walking speed and grip strength in older adults to be associated with higher mortality risk in Cox regression.414243 In this study, analysis of change in motor function between 2007-09 and 2012-13 found decline in both objective (walking speed, grip strength) and self-reported (physical component summary score and limitations in basic/instrumental ADLs) motor function to be associated with increased mortality risk (supplementary table F). However, this approach provides only a mean hazard ratio over the follow-up, which could vary from a few months to several years, rather than change in motor function in the years leading to death. A notable study on “fast” walking speed used a 10 year backwards time scale to show more rapid decline in decedents compared with survivors, but the authors did not do a formal comparison of differences in walking speed in the years leading to death.18 Previous studies have examined terminal decline in ADL limitations over the last few months or years before death.314445 Our data show differences in basic/instrumental ADL limitations to be evident eight years and four years before death (supplementary table I) in analyses unadjusted for chronic conditions and fully adjusted respectively. Terminal decline in physical component summary score, a measure of overall physical functioning, bodily pain, and vitality,24 is rarely examined, and our results on divergence in trajectories four years before death in fully adjusted analyses suggest the usefulness of this measure to monitor motor function.
Meaning of findings
Interest in objective measures of motor function is increasing, reflected in instruments such as the Short Physical Performance Battery (SPPB),46 composed of timed tests of standing balance, walking speed, and chair rises. Performance on this battery has a robust association with mortality.19 In this study, we chose to examine the association of objective and subjective measures of motor function, considering each measure separately, as use of a composite does not allow conclusions to be drawn on the importance of each component because results could be driven by one component or all measures might make a similar contribution. Furthermore, the SPPB does not include self-reported measures, which are easier to measure. Some authors have suggested that measures of upper body function, assessed using a handheld dynamometer, would add to the performance battery,47 but our data do not show substantial differences or terminal decline in grip strength. Our findings also highlight the importance of self-reported measures of motor function.
Motor function is controlled by central and peripheral structures in the nervous system, which include skeletal muscles and neural connections with muscle tissues. Decline in motor function preceding death is likely to be related to disease,48 anomalies in the physiological mechanisms of ageing,49 quantitative and qualitative changes in muscles,50 and more fundamental changes in mitochondria that contribute to accelerated ageing.51 Chronic diseases are thought to be important drivers of motor decline; in this study, adding the multimorbidity score to the analysis attenuated the associations in both time-to-event and backwards trajectories analyses. The importance of chronic diseases might be due to processes of chronic inflammation and oxidative stress; these are likely to operate across the lifecourse,52 as shown by diverging motor function trajectories before death in early old age in our study. However, in our analyses, the association between poorer motor function and increased mortality risk was also observed in participants free of multimorbidity.
The ageing of populations worldwide makes understanding of the functional status of older adults and change in functioning with age important. Research on terminal decline is primarily on cognitive function,9 and when studies examine motor function the focus is on ADL limitations in the last few years of life. Our analysis of trajectories over 10 years in early old age shows the importance of objective and subjective measures of motor function. These results suggest that strategies to reduce accelerated decline should start before old age; early detection of changes in motor function might offer opportunities for prevention and targeted interventions.
What is already known on this topic
Motor function declines with age, with considerable heterogeneity in the rate of decline
In older adults, functional limitations and poorer performance on measures of motor function are associated with higher risk of mortality
Limitations in activities of daily living become common in the last few months or years of life, but whether the difference in motor function trajectories spans a longer time frame is unknown
What this study adds
Poor objective and self-reported motor function, assessed at mean age 65, 69, and 72 years, was associated with higher mortality risk; all associations were stronger with later life measures
Trajectories of motor function over 10 years using a backwards time scale showed terminal decline, increasingly poor motor function in decedents, starting 4-10 years before death
These findings suggest that early detection of changes in motor function might offer opportunities for prevention and targeted interventions
Ethical approval: At each wave, participants provided informed written consent and research ethics approval was obtained from the National Health Service London - Harrow Research Ethics Committee (latest reference number 85/0938).
Data availability statement
Data sharing: Data, protocols, and other metadata of the Whitehall II study are available to the scientific community via either the Whitehall II study data sharing portal (https://www.ucl.ac.uk/epidemiology-health-care/research/epidemiology-and-public-health/research/whitehall-ii/data-sharing) or the DPUK platform (https://www.dementiasplatform.uk/).
We thank all of the participating civil service departments and their welfare, personnel, and establishment officers; the British Occupational Health and Safety Agency; the British Council of Civil Service Unions; all participating civil servants in the Whitehall II study; and all members of the Whitehall II study team. The Whitehall II Study team comprises research scientists, statisticians, study coordinators, nurses, data managers, administrative assistants, and data entry staff, who make the study possible.
Contributors: BL, SS, ASM, and AF developed the hypothesis and study design. BL and AF did the statistical analysis. BL wrote the first and successive drafts of the manuscript. All authors conceived and designed the study, analysed and interpreted the data, and drafted or critically revised the manuscript for important intellectual content, or, in addition, acquired data. ASM and MK obtained funding for the Whitehall II study. BL and AF had full access to the data and take responsibility for the integrity of the data and the accuracy of the data analysis. ASM and SS supervised the study and contributed equally to this work. BL is the guarantor. The corresponding author attests that all listed authors meet authorship criteria and that no others meeting the criteria have been omitted.
Funding: The Whitehall II study is supported by grants from the National Institute on Ageing, NIH (R01AG056477, RF1AG062553); the UK Medical Research Council (R024227, S011676); and the Wellcome Trust (221854/Z/20/Z). SS is supported by the French National Research Agency (ANR-19-CE36-0004-01). MK was supported by NordForsk (75021) and the Academy of Finland (311492). The sponsors had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; and preparation, review, or approval of this manuscript.
Competing interests: All authors have completed the ICMJE uniform disclosure form at http://www.icmje.org/coi_disclosure.pdf and declare; no support from any organisation for the submitted work other than the grants reported in the funding section; no financial relationships with any organisations that might have an interest in the submitted work in the previous three years; no other relationships or activities that could appear to have influenced the submitted work.
The lead author affirms that this manuscript is an honest, accurate, and transparent account of the study being reported; that no important aspects of the study have been omitted; and that any discrepancies from the study as planned (and, if relevant, registered) have been explained.
Dissemination to participants and related patient and public communities: The dissemination plan aims to target a wide audience, including members of the public, patients, and health professionals. It will be achieved using various channels: media outreach via press release from Inserm and University College London, scientific networks, and social media.
Provenance and peer review: Not commissioned; externally peer reviewed.
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