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      Prevalence and patterns of multimorbidity in Australian baby boomers: the Busselton healthy ageing study

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          Abstract

          Background and objective

          Chronic medical conditions accumulate within individuals with age. However, knowledge concerning the trends, patterns and determinants of multimorbidity remains limited. This study assessed the prevalence and patterns of multimorbidity using extensive individual phenotyping in a general population of Australian middle-aged adults.

          Methods

          Participants ( n = 5029, 55% female), born between 1946 and 1964 and attending the cross-sectional phase of the Busselton Healthy Ageing Study (BHAS) between 2010 and 2015, were studied. Prevalence of 21 chronic conditions was estimated using clinical measurement, validated instrument scores and/or self-reported doctor-diagnosis. Non-random patterns of multimorbidity were explored using observed/expected (O/E) prevalence ratios and latent class analysis (LCA). Variables associated with numbers of conditions and class of multimorbidity were investigated.

          Results

          The individual prevalence of 21 chronic conditions ranged from 2 to 54% and multimorbidity was common with 73% of the cohort having 2 or more chronic conditions. (mean ± SD 2.75 ± 1.84, median = 2.00, range 0–13). The prevalence of multimorbidity increased with age, obesity, physical inactivity, tobacco smoking and family history of asthma, diabetes, myocardial infarct or cancer. There were 13 pairs and 27 triplets of conditions identified with a prevalence > 1.5% and O/E > 1.5. Of the triplets, arthritis (> 50%), bowel disease (> 33%) and depression-anxiety (> 33%) were observed most commonly. LCA modelling identified 4 statistically and clinically distinct classes of multimorbidity labelled as: 1) “Healthy” (70%) with average of 1.95 conditions; 2) “Respiratory and Atopy” (11%, 3.65 conditions); 3) “Non-cardiometabolic” (14%, 4.77 conditions), and 4) “Cardiometabolic” (5%, 6.32 conditions). Predictors of multimorbidity class membership differed between classes and differed from predictors of number of co-occurring conditions.

          Conclusion

          Multimorbidity is common among middle-aged adults from a general population. Some conditions associated with ageing such as arthritis, bowel disease and depression-anxiety co-occur in clinically distinct patterns and at higher prevalence than expected by chance. These findings may inform further studies into shared biological and environmental causes of co-occurring conditions of ageing. Recognition of distinct patterns of multimorbidity may aid in a holistic approach to care management in individuals presenting with multiple chronic conditions, while also guiding health resource allocation in ageing populations.

          Supplementary Information

          The online version contains supplementary material available at 10.1186/s12889-021-11578-y.

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          Most cited references41

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          A brief measure for assessing generalized anxiety disorder: the GAD-7.

          Generalized anxiety disorder (GAD) is one of the most common mental disorders; however, there is no brief clinical measure for assessing GAD. The objective of this study was to develop a brief self-report scale to identify probable cases of GAD and evaluate its reliability and validity. A criterion-standard study was performed in 15 primary care clinics in the United States from November 2004 through June 2005. Of a total of 2740 adult patients completing a study questionnaire, 965 patients had a telephone interview with a mental health professional within 1 week. For criterion and construct validity, GAD self-report scale diagnoses were compared with independent diagnoses made by mental health professionals; functional status measures; disability days; and health care use. A 7-item anxiety scale (GAD-7) had good reliability, as well as criterion, construct, factorial, and procedural validity. A cut point was identified that optimized sensitivity (89%) and specificity (82%). Increasing scores on the scale were strongly associated with multiple domains of functional impairment (all 6 Medical Outcomes Study Short-Form General Health Survey scales and disability days). Although GAD and depression symptoms frequently co-occurred, factor analysis confirmed them as distinct dimensions. Moreover, GAD and depression symptoms had differing but independent effects on functional impairment and disability. There was good agreement between self-report and interviewer-administered versions of the scale. The GAD-7 is a valid and efficient tool for screening for GAD and assessing its severity in clinical practice and research.
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            The PHQ-9: validity of a brief depression severity measure.

            While considerable attention has focused on improving the detection of depression, assessment of severity is also important in guiding treatment decisions. Therefore, we examined the validity of a brief, new measure of depression severity. The Patient Health Questionnaire (PHQ) is a self-administered version of the PRIME-MD diagnostic instrument for common mental disorders. The PHQ-9 is the depression module, which scores each of the 9 DSM-IV criteria as "0" (not at all) to "3" (nearly every day). The PHQ-9 was completed by 6,000 patients in 8 primary care clinics and 7 obstetrics-gynecology clinics. Construct validity was assessed using the 20-item Short-Form General Health Survey, self-reported sick days and clinic visits, and symptom-related difficulty. Criterion validity was assessed against an independent structured mental health professional (MHP) interview in a sample of 580 patients. As PHQ-9 depression severity increased, there was a substantial decrease in functional status on all 6 SF-20 subscales. Also, symptom-related difficulty, sick days, and health care utilization increased. Using the MHP reinterview as the criterion standard, a PHQ-9 score > or =10 had a sensitivity of 88% and a specificity of 88% for major depression. PHQ-9 scores of 5, 10, 15, and 20 represented mild, moderate, moderately severe, and severe depression, respectively. Results were similar in the primary care and obstetrics-gynecology samples. In addition to making criteria-based diagnoses of depressive disorders, the PHQ-9 is also a reliable and valid measure of depression severity. These characteristics plus its brevity make the PHQ-9 a useful clinical and research tool.
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              A new equation to estimate glomerular filtration rate.

              Equations to estimate glomerular filtration rate (GFR) are routinely used to assess kidney function. Current equations have limited precision and systematically underestimate measured GFR at higher values. To develop a new estimating equation for GFR: the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation. Cross-sectional analysis with separate pooled data sets for equation development and validation and a representative sample of the U.S. population for prevalence estimates. Research studies and clinical populations ("studies") with measured GFR and NHANES (National Health and Nutrition Examination Survey), 1999 to 2006. 8254 participants in 10 studies (equation development data set) and 3896 participants in 16 studies (validation data set). Prevalence estimates were based on 16,032 participants in NHANES. GFR, measured as the clearance of exogenous filtration markers (iothalamate in the development data set; iothalamate and other markers in the validation data set), and linear regression to estimate the logarithm of measured GFR from standardized creatinine levels, sex, race, and age. In the validation data set, the CKD-EPI equation performed better than the Modification of Diet in Renal Disease Study equation, especially at higher GFR (P < 0.001 for all subsequent comparisons), with less bias (median difference between measured and estimated GFR, 2.5 vs. 5.5 mL/min per 1.73 m(2)), improved precision (interquartile range [IQR] of the differences, 16.6 vs. 18.3 mL/min per 1.73 m(2)), and greater accuracy (percentage of estimated GFR within 30% of measured GFR, 84.1% vs. 80.6%). In NHANES, the median estimated GFR was 94.5 mL/min per 1.73 m(2) (IQR, 79.7 to 108.1) vs. 85.0 (IQR, 72.9 to 98.5) mL/min per 1.73 m(2), and the prevalence of chronic kidney disease was 11.5% (95% CI, 10.6% to 12.4%) versus 13.1% (CI, 12.1% to 14.0%). The sample contained a limited number of elderly people and racial and ethnic minorities with measured GFR. The CKD-EPI creatinine equation is more accurate than the Modification of Diet in Renal Disease Study equation and could replace it for routine clinical use. National Institute of Diabetes and Digestive and Kidney Diseases.
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                Author and article information

                Contributors
                michael.hunter@uwa.edu.au
                Journal
                BMC Public Health
                BMC Public Health
                BMC Public Health
                BioMed Central (London )
                1471-2458
                11 August 2021
                11 August 2021
                2021
                : 21
                : 1539
                Affiliations
                [1 ]Busselton Population Medical Research Institute Inc, Nedlands, WA 6009 Australia
                [2 ]GRID grid.1012.2, ISNI 0000 0004 1936 7910, School of Population and Global Health, The University of Western Australia, ; Crawley, WA 6009 Australia
                [3 ]BPMRI Busselton Health Study Centre, PO Box 659, Busselton, Western Australia 6280
                [4 ]GRID grid.415461.3, ISNI 0000 0004 6091 201X, PathWest Laboratory Medicine of WA, , QEII Medical Centre, ; Nedlands, WA 6009 Australia
                [5 ]GRID grid.3521.5, ISNI 0000 0004 0437 5942, Department of Pulmonary Physiology and Sleep Medicine, , Sir Charles Gairdner Hospital, ; Nedlands, WA 6009 Australia
                [6 ]GRID grid.1012.2, ISNI 0000 0004 1936 7910, Faculty of Health and Medical Sciences, , Medical School, University of Western Australia, ; Crawley, 6009 Australia
                [7 ]GRID grid.1038.a, ISNI 0000 0004 0389 4302, Exercise Medicine Research Institute, Edith Cowan University, ; Joondalup, WA 6027 Australia
                [8 ]GRID grid.1012.2, ISNI 0000 0004 1936 7910, School of Psychological Science, University of Western Australia, ; Perth, WA 6083 Australia
                [9 ]GRID grid.1032.0, ISNI 0000 0004 0375 4078, School of Physiotherapy and Exercise Science, Curtin University, ; Bentley, WA 6845 Australia
                [10 ]GRID grid.3521.5, ISNI 0000 0004 0437 5942, Department of Endocrinology and Diabetes, , Sir Charles Gairdner Hospital, ; Nedlands, WA 6009 Australia
                [11 ]GRID grid.466593.b, ISNI 0000 0004 0636 2475, Ear Science Institute Australia, ; Subiaco, WA 6008 Australia
                [12 ]GRID grid.1012.2, ISNI 0000 0004 1936 7910, Ear Sciences Centre, , The University of Western Australia, ; Crawley, WA Australia
                [13 ]GRID grid.49697.35, ISNI 0000 0001 2107 2298, Department of Speech Language Pathology and Audiology, , University of Pretoria, ; Pretoria, South Africa
                [14 ]GRID grid.415051.4, ISNI 0000 0004 0402 6638, Medical School, University of Western Australia, Fremantle Hospital, ; Fremantle, WA 6959 Australia
                [15 ]GRID grid.1489.4, ISNI 0000 0000 8737 8161, Centre for Ophthalmology and Visual Science, , University of Western Australia, Lions Eye Institute, ; Perth, Australia
                Author information
                http://orcid.org/0000-0001-6704-4815
                https://orcid.org/0000-0001-8874-2305
                https://orcid.org/0000-0003-4730-4645
                https://orcid.org/0000-0002-1653-2496
                https://orcid.org/0000-0002-8856-6046
                https://orcid.org/0000-0002-4915-2254
                https://orcid.org/0000-0001-9987-539X
                https://orcid.org/0000-0002-4468-6097
                https://orcid.org/0000-0003-0302-6129
                https://orcid.org/0000-0002-4207-4724
                https://orcid.org/0000-0002-7786-4128
                https://orcid.org/0000-0002-1766-2612
                https://orcid.org/0000-0002-8723-7574
                https://orcid.org/0000-0002-9979-6867
                https://orcid.org/0000-0003-2911-5381
                https://orcid.org/0000-0003-0749-7411
                https://orcid.org/0000-0001-7914-4709
                https://orcid.org/0000-0002-6018-0547
                Article
                11578
                10.1186/s12889-021-11578-y
                8359115
                34380465
                56fa5bfa-aa6e-46c3-9118-0c54f993941e
                © The Author(s) 2021

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 27 January 2021
                : 30 July 2021
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100003921, Department of Health, Australian Government;
                Funded by: City of Busselton
                Funded by: Government of Western Australia (Department of Jobs, Tourism, Science and Innovation)
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2021

                Public health
                multimorbidity,ageing,co-morbidities,middle-aged,chronic disease
                Public health
                multimorbidity, ageing, co-morbidities, middle-aged, chronic disease

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