Geriatric Syndromes in Older Adults With and Without Diabetes
Geriatric Syndromes in Older Adults With and Without Diabetes
ABSTRACT
PURPOSE: Diabetes prevalence is increasing among older adults globally. The current study aimed to
compare geriatric syndrome prevalence in older adults with and without diabetes.
METHOD: Primary research (2011 to 2024) in English, French, or Spanish was included. We used multiple
databases following Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines.
Pooled log odds ratios (ORs) and prevalence rates were calculated using random-effects models. Sensi-
tivity analysis explored heterogeneity, and publication bias was assessed.
RESULTS: Older adults with diabetes exhibited higher prevalence rates of cognitive impairment (9.13%
vs. 4.22%, log OR: 0.1884), depression (8.96% vs. 5.44%, log OR: 0.3543), falls (11.5% vs. 4.47%, log OR:
0.4237), functional impairment (14.2% vs. 10.6%, log OR: 1.02), urinary incontinence (9.72% vs. 4.35%, log
OR: 1.3668), frailty (22.8% vs. 12.1%, log OR: 1.3443), and polypharmacy (22.9% vs. 5.78%, log OR: 2.5420).
Diabetes was also associated with a higher comorbidity burden.
CONCLUSION: Multidisciplinary strategies addressing diabetes and associated conditions are crucial for
older adults with diabetes. Future research should delve into underlying mechanisms and optimize care
strategies. [Research in Gerontological Nursing, 18(2), 99-108.]
As the global population continues to age, the preva- riatric syndromes encompass a range of conditions, such
lence of chronic conditions among older adults has risen as falls, frailty, cognitive impairment, polypharmacy, and
significantly. Among these conditions, diabetes mellitus incontinence, among others. These syndromes are known
stands out as a major public health concern, with a sub- to be associated with adverse outcomes, including func-
stantial impact on the health and well-being of the older tional decline, hospitalizations, and reduced quality of life
population (International Diabetes Federation [IDF], (Doležalová et al., 2021). Diabetes, on the other hand, is
2017). Concurrently, geriatric syndromes, a collection of characterized by chronic hyperglycemia and systemic met-
multifactorial and interrelated conditions that commonly abolic derangements, leading to a heightened risk of car-
affect older adults, have gained increasing attention in diovascular complications, neuropathy, and microvascular
health care research and practice (Inouye et al., 2007). diseases (Kalra & Sharma, 2018).
The coexistence of diabetes and geriatric syndromes Geriatric syndromes are characterized by a complex in-
presents a complex and challenging clinical scenario. Ge- terplay of medical, psychological, and functional factors.
From Laboratory of Biology and Health, Department of Biology, Faculty of Science, Ibn Tofail University, Kenitra, Morocco.
Disclosure: The authors have disclosed no potential conflicts of interest, financial or otherwise.
Address correspondence to Khadija Elmotia, MPH, Laboratory of Biology and Health, Department of Biology, Faculty of Science, Ibn Tofail Uni-
versity, BP 133, Kenitra 14000, Morocco; email: [Link]@[Link].
Submitted: May 16, 2024. Accepted: December 2, 2024. Published online: January 30, 2025.
doi: 10.3928/19404921-20250115-01
TABLE 2
along with the screening tools commonly used for their as- stitute (JBI) risk of bias assessment tool for cohort studies
sessment. and the JBI checklist for cross-sectional studies, chosen for
its relevance to the research objectives and robustness in
Risk of Bias Assessment evaluating study quality (Moola et al., 2020). Two separate
The quality appraisal process used the Joanna Briggs In- reviewers assessed the data independently using the JBI
RESULTS
Figure 1 provides a visual summary of the study se-
lection process based on the PRISMA guidelines. We ini-
tially identified 720 studies through database and manual
searches. After removing duplicates and screening based
on inclusion and exclusion criteria, we included a total of
Figure 1. Flow chart of study selection. 28 studies for the final meta-analysis. Table D (available in
the online version of this article) presents detailed charac-
tool, focusing on various aspects of data quality, includ- teristics of the included studies, outlining the study design,
ing risk of bias, methodological rigor, and internal validity. sample sizes, gender distribution, mean ages, screening
Data analysis was performed with careful consideration tools used for geriatric syndromes, and quality scores.
given to the potential impact of bias on study findings. In our meta-analysis, we found a clear pattern of in-
Any discrepancies or disagreements between reviewers creased geriatric syndromes among older adults with dia-
were resolved through discussion and consensus-building betes compared to those without diabetes, highlighting the
during research team meetings. The detailed risk of bias additional health challenges this population faces (Table 3).
assessment for each included study is presented in Table C
(available in the online version of this article). Cognitive Impairment
Cognitive impairment was approximately twice as
Strategy for Data Synthesis common in individuals with diabetes, affecting 9% com-
For data synthesis, we used JAMOVI (version 2.3) pared to 4% of older adults without diabetes with a log OR
software to estimate the prevalence, standardized mean of 0.18 (Figure A, available in the online version of this
difference, and log ORs as the outcome measures, with a article). This finding underscores the cognitive decline that
random-effects model applied to the data. The restricted often accompanies diabetes.
maximum-likelihood estimator was used to estimate the
amount of heterogeneity (tau²). The presence of hetero- Depression
geneity was assessed using the Q-test for heterogeneity Similarly, the burden of depression was pronounced,
and the I² statistic. If any heterogeneity was detected (i.e., with 8.96% of older adults with diabetes experiencing de-
tau² > 0), a prediction interval for the true outcomes was pressive symptoms versus 5% in those without diabetes
provided. To identify potential outliers and influential (Figure B, available in the online version of this article).
studies, studentized residuals and Cook’s distances were This finding, indicated by an average log OR of 0.3543,
examined. Studies with Cook’s distances exceeding the highlights the heightened psychological challenges faced
median plus six times the interquartile range of the Cook’s by this population.
distances were considered influential. To assess funnel plot
asymmetry, the rank correlation test and regression test, Falls
using the standard error of the observed outcomes as a pre- The risk of falls also emerged as a critical concern, with
dictor, were conducted. a prevalence of 11% in older adults with diabetes compared
to 4% in their non-diabetic counterparts (Figure C, avail-
Sensitivity Analysis able in the online version of this article). Average log OR of
Sensitivity analysis was used to rigorously assess the 0.42 reinforces the link between diabetes and increased fall
<0.0001
<0.0001
<0.0001
<0.0001
p Value
<0.001
<0.001
0.0112
0.0002
Urinary Incontinence
Urinary incontinence further exemplified
the impact of diabetes, affecting 10% of older
adults with the condition versus 4% without
I2 (%)
92.66
88.35
97.94
99.97
74.68
96.55
100
100
diabetes (Figure D, available in the online ver-
sion of this article). The log OR of 1.37 indi-
Average
Log OR
0.3543
0.18
0.42
1.37
1.02
1.34
2.54
Functional Impairment
Functional impairment was prevalent at
14% among those with diabetes, whereas it
p Value
stood at 11% in individuals without diabe-
0.038
0.007
0.058
0.079
0.069
0.159
tes (Figure E, available in the online version
of this article). The log OR of 1.02 suggests a
positive correlation, calling for functional as-
(%) [95% CI]
Prevalence
12 [–1, 25]
sessments in diabetes management.
11 [1, 23]
6 [–2, 14]
Diabetes
Without
5 [0, 11]
4 [1, 8]
4 [1, 8]
4 [0, 9]
Frailty
Frailty was markedly higher in older
adults with diabetes, with a prevalence of 23%
TABLE 3
p Value
<0.001
<0.001
0.006
0.003
0.002
0.041
0.078
compared to 12% in those without diabetes
(Figure F, available in the online version of this
article). This substantial difference, reflected in
a log OR of 1.34, highlights the vulnerability
8.96 [2.6, 15.3]
With Diabetes
(%) [95% CI]
Prevalence
23 [11, 35]
23 [–3, 48]
11 [4, 19]
10 [4, 16]
14 [1, 28]
care approaches.
Polypharmacy
Diabetes (n)
Participants
447,671
369,208
132,451
324,532
31,355
70,165
10,723
22,804
Note. CI = confidence interval; OR = odds ratio; SMD = standardized mean difference.
14,195
29,497
40,520
9,921
1,901
7,211
Comorbidity
16
12
15
7
6
6
Comorbidity
impairment
impairment
Depression
Functional
Urinary
Frailty
Location
Section and Item
Checklist item where item
Topic # is reported
TITLE
Title 1 Identify the report as a systematic review. 1
ABSTRACT
Abstract 2 See the PRISMA 2020 for Abstracts checklist. 1
INTRODUCTION
Rationale 3 Describe the rationale for the review in the context of existing knowledge. 2
Objectives 4 Provide an explicit statement of the objective(s) or question(s) the review addresses. 3
METHODS
Eligibility criteria 5 Specify the inclusion and exclusion criteria for the review and how studies were grouped for the syntheses. 5
Information 6 Specify all databases, registers, websites, organizations, reference lists and other sources searched or consulted to identify studies. Specify the date when 4
sources each source was last searched or consulted.
Search strategy 7 Present the full search strategies for all databases, registers and websites, including any filters and limits used. 4
8 Specify the methods used to decide whether a study met the inclusion criteria of the review, including how many reviewers screened each record and each 4
Selection process
report retrieved, whether they worked independently, and if applicable, details of automation tools used in the process.
9 Specify the methods used to collect data from reports, including how many reviewers collected data from each report, whether they worked 4
Data collection
process independently, any processes for obtaining or confirming data from study investigators, and if applicable, details of automation tools used in the process.
10a List and define all outcomes for which data were sought. Specify whether all results that were compatible with each outcome domain in each study 5-7
were sought (e.g. for all measures, time points, analyses), and if not, the methods used to decide which results to collect.
Data items 6
10b List and define all other variables for which data were sought (e.g. participant and intervention characteristics, funding sources). Describe any
assumptions made about any missing or unclear information.
Study risk of bias 11 Specify the methods used to assess risk of bias in the included studies, including details of the tool(s) used, how many reviewers assessed each study and 8
assessment whether they worked independently, and if applicable, details of automation tools used in the process.
Effect measures 12 Specify for each outcome the effect measure(s) (e.g. risk ratio, mean difference) used in the synthesis or presentation of results. 4
13a Describe the processes used to decide which studies were eligible for each synthesis (e.g. tabulating the study intervention characteristics and comparing 5-6
against the planned groups for each synthesis (item #5)).
13b Describe any methods required to prepare the data for presentation or synthesis, such as handling of missing summary statistics, or data 8
conversions.
Synthesis 13c Describe any methods used to tabulate or visually display results of individual studies and syntheses. 8
methods
13d Describe any methods used to synthesize results and provide a rationale for the choice(s). If meta‐analysis was performed, describe the model(s), 8
method(s) to identify the presence and extent of statistical heterogeneity, and software package(s) used.
13e Describe any methods used to explore possible causes of heterogeneity among study results (e.g. subgroup analysis, meta‐regression). 8
13f Describe any sensitivity analyses conducted to assess robustness of the synthesized results. 8
Reporting bias 14 Describe any methods used to assess risk of bias due to missing results in a synthesis (arising from reporting biases). 8
assessment
Certainty 15 Describe any methods used to assess certainty (or confidence) in the body of evidence for an outcome. 8
assessment
Location
Section and Item
Checklist item where item
Topic # is reported
RESULTS
Study selection 16a Describe the results of the search and selection process, from the number of records identified in the search to the number of studies included in the review, 9
ideally using a flow diagram.
16b Cite studies that might appear to meet the inclusion criteria, but which were excluded, and explain why they were excluded. 9
Study 17 Cite each included study and present its characteristics. 10-13
characteristics
Risk of bias in 18 Present assessments of risk of bias for each included study. 10-13
studies
Results of 19 For all outcomes, present, for each study: (a) summary statistics for each group (where appropriate) and (b) an effect estimates and its precision 10-13
individual studies ([Link]/credible interval), ideally using structured tables or plots.
Results of 20a For each synthesis, briefly summarize the characteristics and risk of bias among contributing studies. 10-13
syntheses 20b Present results of all statistical syntheses conducted. If meta‐analysis was done, present for each the summary estimate and its precision (e.g. 14-18
confidence/credible interval) and measures of statistical heterogeneity. If comparing groups, describe the direction of the effect.
20c Present results of all investigations of possible causes of heterogeneity among study results. 14-18
20d Present results of all sensitivity analyses conducted to assess the robustness of the synthesized results. 14-18
Reporting biases 21 Present assessments of risk of bias due to missing results (arising from reporting biases) for each synthesis assessed. 14-18
Certainty of 22 Present assessments of certainty (or confidence) in the body of evidence for each outcome assessed. 14-18
evidence
DISCUSSION
Discussion 23a Provide a general interpretation of the results in the context of other evidence. 19-20
23b Discuss any limitations of the evidence included in the review. 21
23c Discuss any limitations of the review processes used. 21
23d Discuss implications of the results for practice, policy, and future research. 19-20
OTHER INFORMATION
Registration and 24a Provide registration information for the review, including register name and registration number, or state that the review was not registered. 4
protocol 24b Indicate where the review protocol can be accessed, or state that a protocol was not prepared. 4
24c Describe and explain any amendments to information provided at registration or in the protocol. 4
Support 25 Describe sources of financial or non‐financial support for the review, and the role of the funders or sponsors in the review. 22
Competing 26 Declare any competing interests of review authors. 22
interests
Availability of 27 Report which of the following are publicly available and where they can be found: template data collection forms; data extracted from included studies; _
data, code and data used for all analyses; analytic code; any other materials used in the review.
other materials
Table B. Complete Search Strategy
Embase ('diabetes mellitus'/exp OR 'type 2 diabetes'/exp) AND No filters, From April 1, 250
('cognitive dysfunction'/exp OR 'depression'/exp OR Humans, 2023, to
'falls'/exp OR 'frailty'/exp OR 'polypharmacy'/exp OR Adults aged January 30,
'comorbidity'/exp OR 'urinary incontinence'/exp) 65+ 2024
Manual Reference lists from key articles and review papers N/A From April 1, 50
Search 2023, to
January 30,
2024
Table C. JBI Critical Appraisal Score
Were the Were the Was the Were Were Were Were the Was Quality
criteria for study exposure objective, confou strategies to outcomes appropri score
ate
inclusion in the subjects and measured in standard nding deal with measured in statistica
sample clearly the setting a valid and criteria used factors confounding a valid and l analysis
Study (cross-sectional) used?
defined? described in reliable for identifi factors reliable way?
detail? way? measurement ed? stated?
of the
condition?
Abodo et al., (2017) Yes Yes Yes Yes Yes Yes Yes Yes 8
Aguayo et al., 2019 Yes Yes Yes Yes Yes Yes Yes Yes 8
Argano et al., 2022 Yes yes Yes Yes Yes Yes Yes Yes 8
Yes Yes Yes Yes Yes Yes Yes Yes 8
Cacciatore, et al. 2013
Carmienke et al., 2020 Yes Yes Yes Yes Yes Yes Yes Yes 8
Yes Yes Yes Yes Yes Yes Yes Yes 8
Casagrande et al., 2021
Chau et al., 2011 Yes Yes Yes Yes Yes Yes Yes Yes 8
Cigolle et al., 2011 Yes Yes Yes Yes Yes Yes Yes Yes 8
Dybicz et al., 2011 Yes Yes Yes Yes Yes Yes Yes Yes 8
Forbes et al., 2017 Yes No Yes Yes Yes Yes Yes Yes 8
Huang et al., 2021 Yes Yes Yes Yes Yes Yes Yes Yes 8
Karjalainen, 2021 Yes Yes Yes Yes Yes Yes Yes Yes 8
Karjalainen et al., 2018 Yes Yes Yes Yes Yes Yes Yes Yes 8
Karsli et al., 2022 Yes Yes Yes Yes Yes Yes Yes Yes 8
Kera et al., 2018 Yes Yes Yes Yes Yes Yes Yes Yes 7
Kitamura et al., 2019 Yes Yes Yes Yes Yes Yes Yes Yes 8
Kotsani et al., 2018 Yes Yes Yes Yes Yes Yes Yes Yes 8
Li et al., 2013 Yes Yes Yes Yes Yes Yes Yes Yes 8
Thein et al., 2018 Yes Yes Yes Yes Yes Yes Yes Yes 8
Varghese et al., 2017 Yes Yes Yes Yes Yes Yes Yes Yes 8
Wallander et al., 2017 Yes Yes Yes Yes Yes Yes Yes Yes 8
Wojszel & Magnuszewski, 2020 Yes Yes Yes Yes Yes Yes Yes Yes 8
Yes Yes Yes Yes Yes Yes Yes Yes 8
Zghebi et al., 2020
Table C. JBI Critical Appraisal Score (continued)
Study Groups Exposures Exposure Confounding Strategies to Participants Outcome Follow-up Complete Strategies Appropriate Score
(Cohort) Similar & Measured Measurement Factors Deal with Free of Measurement Time Follow-up for Statistical
Recruited Similarly? Valid & Identified? Confounding? Outcome at Valid & Reported or Reasons Incomplete Analysis?
from Same Reliable? Start? Reliable? & Explained? Follow-
Population? Sufficient? up?
Aguayo Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes 11
et al.,
2019
Forbes et Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes 11
al., 2017
Kitamura Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes 11
et al.,
2019
Lekan & Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes 11
McCoy,
2018
Panahi et Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes 11
al., 2024
Zghebi et Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes 11
al., 2020
Table D. Study Characteristics
Study Country Study Design Sample Size Female Male Mean Age Screening Tools Quality
With Without With Without With Without With Without Score
Diabetes Diabetes Diabetes Diabetes Diabetes Diabetes Diabetes Diabetes
Abodo et al., Ivory Cross- 145 150 NG NG NG NG 79.6 81.2 Mini-GDS 8
2017 Coast sectional MMSE
ADL
Aguayo et Denmark Cohort 635 4,742 46% 57% 54% 43% 72 70 EFS 11
al., 2019
Argano et al., Italy Cross- 1378 3330 NG NG 56.2% 43.8 % 78.45 79.68 GDS 8
2022 sectional Barthel Scale
Short Blessed
Test score
Cacciatore et 188 1,100 67.0% 55.3% 33.0% 44.7 72.8 74.3 FSS 8
Cross-
al., 2013 Italy GDS
sectional
MMSE
Carmienke et Germany Cross- 248 692 58.5% 59.7% 41.5 40.3 73.4 72.7 Coop-Wonca – 8
al., 2020 sectional Charts
STEP
Questionnaire
208 999 49.5 % 58.9% 50.5% 41.1% NG NG CERAD W-L 8
Casagrande
Cross- DSST
et al., 2021 USA
sectional PHQ-9
Chau et al., China Cross- 9,222 57,591 6,130 38,007 3,092 19,584 Abbreviated 8
2011 sectional (86.1%) (86.4%) Mental Test—
Hong Kong
GDS
IADL
ADL
Cigolle, et USA longitudinal 3,506 15,402 52.1% 57.7% 47.9 42.3 NG NG MMSE 8
al., 2011 health ADL
interview IADL
survey data
Dybicz et al., USA Retrospective 761 1556 30.8% 69.2% 38.2% 61.8% NG NG CPS 8
2011 observational Activities of
Daily Living
Domain Scale
(ADL DS)
Forbes et al., UK Cohort 35,717 307,918 52.3% 60.7% 47.7% 39.3 78.13 78.98 Comorbidity 11
2017 index
Polypharmacy
> 5 drugs per
day
Huang et al., UK Cross- 1100 6629 49.3% 56.4% 50.7% 43.6% 70.0 67.2 Polypharmacy 8
2021 sectional >5 drugs
long term
medication per
day
Karjalainen, Finland Cross- 389 604 50.8% 54.4% 49.2% 45.6% 75 77 GDS 8
2021 sectional
Karjalainen Finland Cross- 389 604 50.8% 54.4% 49.2% 45.6% 75 74 GDS 8
et al., 2018 sectional
Karsli et al., Turkey Cross- 149 149 67.1% 59.7% 32.9% 40.3% 70.38 70.97 EFS 8
2022 sectional
At least one
fall in the last
year
Kera et al., Japan Cross- 705 984 56.1% 59.2% 43.9 40.8 72.1 71.3 Grip strength 8
2018 sectional TUG
MMSE
Kitamura et Japan Cohort 181 1090 47% 63% 53% 37% 71.0 72.1 MMSE 11
al., 2019 GDS
Grip strength
TUG
Kotsani et al., Greece Cross- 198 205 55.1% 54.6% 44.9% 45.4% 72.9 74.0 TUG 8
2018 sectional GDS
MMSE
Global
Disability
Scale (GloDiS)
Li et al., Taiwan Cross- 473 2251 56.4% 48.2% 43.6% 51.8% NG NG ADL, IADL 8
2013 sectional GDS
MMSE
Cross- 2,395 7,904 61.0% 59.5% 39.0% 40.5% 74.6 74.6 MMSE 8
sectional Polypharmacy:
≥5 drugs for 3
months
Falls: one or
Moon et al., more falls over
2019 Korea 1 year
GDS
Urinary
incontinence:
diagnosed
incontinence
for ≥3 months
Nezu et al., Japan Cross- 572 3374 36.0% 52.0% 64.0% 48% 72.0 72.0 Japanese version of 8
2014 sectional the Medical Outcomes
Study 36-Item Short-
Form General Health
Survey Version 2.0
(SF-36 v2)
Thein et al., Singapore Cross- 486 2210 59.5% 63.5% 40.5% 36.5% 67.3 65.6 MMSE 8
2018 sectional POMA
ADL
IADL
Varghese et India Cross- 406 744 36.7% 34.1% 63.3% 65.9% 68.2 68.5 GDS 8
al., 2017 sectional SPMSQ
At least one
fall in the last
year
Wallander et Sweden Cohort 84,702 343,603 50% 59% 50% 41% 79.3 81.1 Charlson 11
al., 2017 Comorbidity
Index
Self-reported
fall injury
Wojszel & Poland Cross- 126 290 73.8% 79% 26.2% 21.0% 81 82.5 AMTS 8
Magnuszews sectional GDS
ki, 2020 Barthel Index
Clinical Frailty
Scale
10,202 49,589 NG NG NG NG NG NG Read/ICD-10 11
Zghebi et al., diagnostic
UK Cohort
2020 code
Figure A1. Prevalence of cognitive impairment in older adults without diabetes.
Figure A2. Prevalence of cognitive impairment in older adults with diabetes.
Figure A3. Pooled log odds ratio for cognitive impairment.
Figure B1. Prevalence of depression in older aduls without diabetes.
Figure B2. Prevalence of depression in older aduls with diabetes.
Figure B3. Pooled log odds ratio for depression.
Figure C1. Prevalence of falls in older adults with diabetes.