About the Authors:
Carl Bonander
Roles Conceptualization, Data curation, Formal analysis, Funding acquisition, Methodology, Project administration, Visualization, Writing – original draft
* E-mail: [email protected]
Affiliation: School of Public Health and Community Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden
ORCID logo https://orcid.org/0000-0002-1189-9950
Anton Nilsson
Roles Conceptualization, Formal analysis, Methodology, Writing – review & editing
Affiliations Epidemiology, Population Studies and Infrastructures (EPI@LUND), Lund University, Lund, Sweden, Centre for Economic Demography, Lund University, Lund, Sweden
ORCID logo https://orcid.org/0000-0001-5774-7189
Jonas Björk
Roles Conceptualization, Methodology, Writing – review & editing
Affiliations Epidemiology, Population Studies and Infrastructures (EPI@LUND), Lund University, Lund, Sweden, Clinical Studies Sweden, Forum South, Skåne University Hospital, Lund, Sweden
Anders Blomberg
Roles Funding acquisition, Investigation, Project administration, Resources, Writing – review & editing
Affiliation: Department of Public Health and Clinical Medicine, Section of Medicine, Umeå University, Umeå, Sweden
Gunnar Engström
Roles Funding acquisition, Investigation, Project administration, Resources, Writing – review & editing
Affiliation: Department of Clinical Sciences, Lund University, Malmö, Sweden
Tomas Jernberg
Roles Funding acquisition, Investigation, Project administration, Resources, Writing – review & editing
Affiliation: Department of Clinical Sciences, Danderyd University Hospital, Karolinska Institutet, Stockholm, Sweden
Johan Sundström
Roles Funding acquisition, Investigation, Project administration, Resources, Writing – review & editing
Affiliations Department of Medical Sciences, Clinical Epidemiology, Uppsala University, Uppsala, Sweden, The George Institute for Global Health, University of New South Wales, Sydney, Australia
Carl Johan Östgren
Roles Funding acquisition, Investigation, Project administration, Resources, Writing – review & editing
Affiliation: Department of Health, Medicine and Caring Sciences, Linköping University, Linköping, Sweden
Göran Bergström
Roles Conceptualization, Funding acquisition, Investigation, Project administration, Resources, Supervision, Writing – review & editing
Affiliations Department of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden, Department of Clinical Physiology, Sahlgrenska University Hospital, Region Västra Götaland, Gothenburg, Sweden
Ulf Strömberg
Roles Conceptualization, Data curation, Funding acquisition, Investigation, Methodology, Project administration, Supervision, Writing – review & editing
Affiliation: Department of Research and Development, Region Halland, Halmstad, Sweden
Introduction
Selective participation is a general concern in population-based research that aims to make inferences about health outcomes or exposure effects in the general population [1]. For instance, the population-based Swedish CardioPulmonary bioImage Study (SCAPIS, www.scapis.org) aims to improve risk prediction of cardiopulmonary diseases and study disease mechanisms in a general middle-aged population [2]. The study combines new imaging techniques with advanced large‐scale ‘omics’ and epidemiological analyses to characterize a population-based cohort, and is expected to provide new evidence about the prevalence of hidden cardiopulmonary disease and improved prediction models for the general population. To fulfill these aims, the participants of SCAPIS must reflect their intended target population.
However, cohort studies that rely on voluntary clinical examinations tend to be skewed towards healthy individuals with high socioeconomic status [3, 4], and SCAPIS is no exception [5, 6]. This type of non-random participation can pose a severe threat to the internal and external validity of study results [1, 7, 8]. A lack of internal validity implies spurious correlations between exposures (or treatments) and health outcomes [7], and a lack of external validity implies poor generalizability of the study results to the intended target population [1]. These problems may negatively influence the utility of the research findings for public health decision-making [9]. However, they can potentially be remedied by reweighting the study sample to match the intended target population on sociodemographic characteristics using inverse propensity for participation weights [10–13]. Constructing such weights typically requires access to external data on non-participants or (a random sample of) the target population [6, 14].
Population registers with high coverage, such as those available in the Nordic countries, enable linkage of sociodemographic data to each study participant and member of the target population [14]. Such register infrastructures are generally not available in other settings, which presents a challenge for high-quality participation modeling and subsequent adjustment for selective participation. However, previous validation studies have found that using individual-level register data to account for selective participation was able to improve the external validity of study results in some cases [15], but not others [12], indicating that important differences may remain even with access to rich individual-level data on patient histories and sociodemographics.
Collecting neighborhood-level data on the population may serve as a more practical alternative while retaining a relatively high precision in settings where individual-level data cannot be accessed [16, 17]. While neighborhood data alone cannot fully capture and adjust for individual-level selection effects [16], it may also encode contextual influences on participation, risk factors, and health outcomes [18]. Combining data on individual sociodemographic profiles and neighborhood conditions may help account for selection effects beyond those that individual- or neighborhood-level data can account for separately. To our knowledge, only one previous study has directly compared the use of individual-level and aggregate data for handling selective participation; that study focused on statistical approaches that use aggregate summary-level statistics and compared them to a gold-standard individual-level approach [17]. The findings suggested that while individual-level data are preferable, aggregate data can also be leveraged to improve external validity. However, the focus of that study was not on combining data at both levels, and it did not consider neighborhood-level data at a fine scale.
The Swedish register infrastructure, which contains rich information on the entire population [19], provides a useful setting for evaluating the use of individual and area-level data for improving the external validity of study results, both on their own and in combination. The objective of the present study was to investigate the value of combining individual-level and area-level sociodemographic register data for predicting study participation in the context of the Swedish register infrastructure, using the Swedish CardioPulmonary bioImage Study (SCAPIS) as a case study. We also applied the method to assess the potential effects of baseline selection on the distribution of metabolic risk factors and lifestyle factors, which will help inform future research about potential biases caused by selective participation in SCAPIS.
Methods
Recruitment and participation in SCAPIS
The recruitment strategy and overall design of the SCAPIS cohort are documented in detail elsewhere [2] and will only be briefly summarized here. To recruit study participants for SCAPIS, written invitations were sent to 59,909 randomly selected men and women between 50 and 64 years of age living in the areas surrounding six university hospitals in Sweden. Of the invited individuals, 30,154 (50.3%) agreed to participate, and baseline clinical examinations were completed between 2013 and 2018. Site-specific details are provided in Table 1.
[Figure omitted. See PDF.]
Table 1. Participation and recruitment into the Swedish CardioPulmonary bioImage Study (SCAPIS) by site and in total.
https://doi.org/10.1371/journal.pone.0265088.t001
Data collection
The present study combines external individual- and neighborhood-level register data on the participants of SCAPIS with data from a random sample of the target population living in the same areas, at the same time, as those invited to participate in the cohort study (Table 1). Specifically, the target population consists of individuals aged 50 to 64 years living in one of the 1,925 demographic statistical areas (DeSO [In Swedish: Demografiska statistikområden]) surrounding the university hospitals that were included in SCAPIS (out of the 5,984 DeSOs in Sweden; see the map in S1 Fig in S1 Appendix for reference) sometime between 2013 and 2018 depending on site (see Table 1 for details). The DeSO geography is one of the finer geographical divisions available in Sweden. It was created by Statistics Sweden with the intention of monitoring segregation and socioeconomic conditions in small areas, which makes it especially useful for capturing variation in socioeconomic deprivation at the area level [20]. Throughout the study period (2013–2018), approximately 280 individuals aged 50 to 64 years lived in an average DeSO within the study area (range: 2–546; interquartile range: 229–333). To simplify the presentation, we will refer to DeSOs as neighborhoods throughout the rest of the paper.
The Swedish Total Population Register covers the entire Swedish population and includes information such as age, country of birth, and place of residence [21]. Based on this register, Statistics Sweden provided anonymized data on the study area population from 2013 to 2018, from which we drew a random sample of individuals (n = 59,909) to represent the target population of SCAPIS. The sample was drawn with the same sampling probabilities from the same neighborhoods and recruitment periods as those invited to participate in SCAPIS (Table 1) and therefore represents the same target population as those invited to participate in the study [14]. For each member of the target population, we also received individual-level data on income divided into three groups based on household disposable income per consumption unit (‘low’, income in the lowest quartile of the households in Sweden; ‘medium’, income in quartiles 2 and 3; and ‘high’, income in the highest quartile) and immigrant group (three groups according to country of birth: the Nordic countries, other Western countries, and non-Western countries, the latter referring to inhabitants born in Eastern Europe, Asia, Africa or South America). Statistics Sweden also linked corresponding data to the SCAPIS participants via Swedish personal identification numbers [22]. The individual-level variables were derived from the Income and Taxation Register and the Total Population Register, which contain data on all Swedish taxpayers and the entire population, respectively.
In addition to the individual-level information, we also linked data on neighborhood-level aggregates of the above-mentioned income and immigrant groups (percentages of the population aged 50–64 years in each group) to each individual, in addition to the following indicators of neighborhood socioeconomic conditions obtained from Statistics Sweden: the percentage of individuals aged 50–64 years with a university degree, the percentage of unemployed working-age individuals, the percentage of single-parent households (all ages), and the percentage of the population living in rental housing (all ages).
Statistical analysis
Estimation of propensity scores for participation.
We used multivariable logistic regressions to model participation in a stacked dataset containing both the participants and the population sample (n = 30,154+59,909 = 90,063). With this data structure, the estimated odds of belonging to the participant sample in the data set can be interpreted as the estimated propensity score (i.e., probability) for participation [14]. We note that a practical issue that may arise with this approach is that the estimated propensity score may sometimes exceed one by chance; in the few cases when this occurred (0 to 0.12% of observations depending on the model), a score of one was assigned for simplicity. The regression models were estimated in R (version 4.0.4; R Core Team, Vienna, Austria).
Model assessment and comparison.
We assessed the classification ability of regression models based on individual-level sociodemographics only, area-level data only, and a combination of data from both levels.
The individual-level model contained the following individual-level characteristics: age, sex, income, and country of birth. The area-level model contained the following neighborhood-level characteristics: site, percentage of households with low and middle income, percentage of the population of non-Nordic and non-Western origin, percentage with a university education, percentage living in rental housing, percentage of unemployed working-age individuals, and the percentage of single-parent households (percentage of high-income households and percentage of Nordic origin were omitted to avoid collinearity with the other income and country of birth categories). The combined model contained all characteristics included in the individual-level and area-level models.
In addition to these models, we also estimated a model with spline terms to assess deviations from non-linearity for continuous variables and a model with two-way interactions between all variables.
We calculated the area under the receiver operating characteristic curve (AUC) using an approach developed for participation modeling with stacked datasets [23] (see S1 Appendix for details). The AUC calculations were performed in Stata (version 16.1; StataCorp LLC, College Station, Texas).
Assessment of changes in cardiopulmonary risk factors after reweighting.
We used the combined model with two-way interactions to compute inverse probability for participation weights for the SCAPIS participants. These weights were then used to examine changes in the distribution of 32 cardiopulmonary risk factors (see results section for details; data collection procedures used in SCAPIS are detailed elsewhere [2]).
To facilitate comparison between variables of different scales, we computed standardized differences using methods appropriate for categorical and continuous variables [24, 25], which is the recommended approach for assessing covariate balance between groups (e.g., a sample and a population) and between unweighted and weighted samples [24]. An absolute standardized difference above 0.10 is typically used as a reference point to indicate a meaningful covariate imbalance [26], where 0.10 can be read as 10% of one standard deviation of the variable in question.
Ethics statement
This project has been approved by the Regional Ethics Committee in Umeå (diary number 2010-228-31M, with addendum 2011-02-21, for SCAPIS and diary number 2016-511-31 for the linkage of register data to SCAPIS participants). Written informed consent was obtained from all SCAPIS participants.
Statistics Sweden delivered the population data to us in aggregate form (the individual-level information was recreated from stratified counts). These data cannot be linked to any living person and does not constitute sensitive personal data, and their use is therefore exempt from the need for ethics approval according to the Swedish Ethical Review Act (2003:460).
Results
The standardized differences between SCAPIS participants and the target population exceeded a magnitude of 0.10 in 12 out of 15 sociodemographic characteristics (Table 2). The most considerable differences were related to income and country of birth at both the individual and neighborhood levels, followed by neighborhood-level unemployment, single-parent households, rental housing, and university education (Table 2). As determined by these characteristics, SCAPIS participants appeared to have higher individual socioeconomic status and live in more affluent neighborhoods than the target population and non-participants of the SCAPIS study. We also note that the SCAPIS participants were, on average, slightly older than the target population (33% in the age range 50–54 years in SCAPIS, 37% in the target population).
[Figure omitted. See PDF.]
Table 2. Sociodemographic characteristics of the participants in the Swedish CardioPulmonary bioImage Study (SCAPIS), a random sample of its target population, and inferred characteristics of the non-participants of the study.
https://doi.org/10.1371/journal.pone.0265088.t002
The results from the individual-level, neighborhood-level, and combined multivariable logistic regression models for predicting participation in SCAPIS are presented in Table 3. Histograms of the predicted probabilities can be found in S2 Fig in S1 Appendix. The classification ability (AUC) of the models based only on individual-level or neighborhood-level characteristics were 66.9% and 65.5%, respectively. Combining characteristics from both levels improved the classification ability (AUC: 70.2%). Notably, both individual and neighborhood-level socioeconomic conditions independently predicted participation in the combined model (for instance, the neighborhood percentage of low-income individuals was predictive of participation in SCAPIS even when adjusting for income at the individual level) (Table 3). Including interactions between all included variables and cubic splines to account for potential non-linearity in continuous variables only marginally improved the model’s classification ability (AUC: 71.1%; 70.3%, respectively). Predicted probabilities from the combined model with interactions varied considerably within strata defined by the individual-level characteristics and site (e.g., from almost zero to approximately 30% among 60 to 64-year-old women of non-Western origin with low incomes within the same city [Uppsala]; S3 Fig in S1 Appendix).
[Figure omitted. See PDF.]
Table 3. Results from logistic regression models predicting participation in SCAPIS, with coefficients expressed as odds ratios with 95% confidence intervals in parentheses.
https://doi.org/10.1371/journal.pone.0265088.t003
Comparisons of absolute standardized differences between SCAPIS participants and the target population before and after weighting using the estimated propensity scores from the individual-level, neighborhood-level, and combined models, are presented in Fig 1 (detailed data can be found in S1-S3 Tables in S1 Appendix). As expected, weights based on individual-level data could not balance neighborhood-level characteristics and vice versa. Balance was achieved on all observed characteristics in the combined model, indicating sufficient overlap in covariate distributions between the sample and population to standardize the participants to match the target population.
[Figure omitted. See PDF.]
Fig 1.
Balance (in absolute standardized differences) between SCAPIS participants and the target population before and after inverse probability for participation weighting based on (a) individual characteristics, (b) neighborhood characteristics and (c) the combination of both. The variables are ordered from largest to smallest unweighted standardized difference with variable groups (individual [Ind.] and neighborhood [Area]). The standardized difference, averaged over all included variables before and after weighting within variable groups, are illustrated with dashed and solid vertical lines, respectively.
https://doi.org/10.1371/journal.pone.0265088.g001
We applied the weights from the model with individual factors only, area-level factors only, and the combined model with two-way interactions to study changes in 32 cardiopulmonary risk factors measured at baseline. Standardized differences between the weighted and unweighted SCAPIS participants from each model are presented in Fig 2, where an increase (positive difference) suggests that the target population has a higher mean value or prevalence (depending on the type of variable) than the participants, and a decrease (negative difference) indicates the opposite. Overall, we find that most risk factors changed more substantially when we reweighted the participants using individual and neighborhood-level sociodemographics than using individual or neighborhood data alone (Fig 2). However, even when using weights based on data from both levels, only one determinant (self-reported frequency of alcohol consumption) decreased by more than 0.10 (25% reported drinking once a month or less in SCAPIS versus an estimated 30% in the target population). The remaining factors changed less meaningfully. Two decreased with a magnitude between 0.05 to 0.10 (alcohol consumption in grams per day [7.11 vs. 6.52 g/day on average] and high-density lipoprotein [HDL] cholesterol levels [1.63 vs. 1.59 mmol/L], and five increased with a magnitude between 0.05 and 0.10 (current smokers [12% vs. 14%], dyspnea [9.5% vs. 11.6%], body mass index [27.0 vs. 27.2 kg/m2], triglyceride levels [1.25 vs. 1.29 mmol/L], and estimated glomerular filtration rate [85.1 vs. 85.9 ml/min/1.73 m2]). The remaining 24 determinants changed with a magnitude of less than 0.05 (Fig 2). These changes were similar within age groups (S4-S6 Figs in S1 Appendix), indicating that the observed changes are not only driven by the difference in age structure between the sample and population and that socioeconomic conditions also play a key role. Detailed descriptive statistics for each determinant before and after weighting based on the combined individual- and neighborhood-level weights can be found in S4 Table in S1 Appendix.
[Figure omitted. See PDF.]
Fig 2. Standardized differences between the unweighted SCAPIS participants and weighted SCAPIS participants standardized to match the target population on individual and neighborhood-level sociodemographic characteristics.
The horizontal lines show by much the mean changes after reweighting the data using three sets of weights (based on area data only, based on individual data only, or based on both). The vertical reference lines at -0.10, -0.05, 0.05 and 0.10 highlight potentially meaningful differences. An increase in mean (or prevalence, depending on variable type) suggests that the mean is greater in the target population than among SCAPIS participants. A decrease suggests the opposite (i.e., that the estimates incidate a lower mean in the target population relative to SCAPIS participants).
https://doi.org/10.1371/journal.pone.0265088.g002
Discussion
Our study demonstrates the potential usefulness of combining individual-level register data on sociodemographic characteristics with neighborhood-level data to improve the validity of study results in the presence of selective participation. Notably, our combined model showed a comparable classification ability to a participation model developed for the pilot phase of SCAPIS (AUC: 71.1% versus 73.2%) [6], which used considerably more detailed individual-level data on sociodemographic and disease histories.
Together with related research [17], our study provides quantitative insight into the relative importance of individual- and neighborhood-level data in study participation models. Importantly, meaningful differences in income and country of birth remained in our data after adjustment for neighborhood-level characteristics, suggesting that weights based on neighborhood-level data may fail to capture individual-level selection effects. This result highlights a potential problem with using only neighborhood-level data to address selection issues, especially since disease outcomes are more strongly associated with individual-level lifestyle factors than area-level factors [27]. Conversely, another key implication from our study is that the addition of neighborhood characteristics may substantially improve the quality of the participation model even when individual-level data are available. We also found a larger shift in the risk factor distribution when using weights based on the combination of individual- and neighborhood-level data than when using weights based on either data source alone. These results imply that one may leverage area-level information to improve the validity of study results even if individual-level data are available. However, additional research is required to assess how these results extend to other contexts and area-level data at other scales (e.g., less fine-scaled geographical units).
The results also have implications for research based on SCAPIS (and similar cohort studies). One important takeaway is that the SCAPIS participants appear reasonably similar to the target population on the distribution of baseline risk factors. If anything, our weighted estimates suggest that the validity of analyses related to self-reported alcohol consumption and, to a lesser extent, renal function, body mass index, dyspnea, and smoking may be affected by selective participation. Specifically, SCAPIS participants appear to consume alcohol more frequently, although the difference could potentially be explained by socioeconomic differences in self-reporting bias [28]. The frequency of alcohol consumption should also not be confused with a higher prevalence of problem drinking [29], which did not differ as much between the sample and population according to our estimates (Fig 2). We note, however, that a recent study examining the effects of selection in the UK Biobank found that the association between alcohol consumption and cardiovascular disease seems to be particularly affected by sample selection [30].
The prevalence of current smokers also appears to be lower in the SCAPIS sample than in the target population. This measure is also self-reported, but bias in self-reported smoking does not appear to be as sensitive to socioeconomic status as measures of alcohol use [31]. The SCAPIS participants also seem to have a slightly lower body mass index and renal function (measured by estimated glomerular fibrillation rates [32]) and a lower prevalence of dyspnea. Overall, the directions of change in these factors after weighting the sample to match a less advantaged target population are generally in line with our expectations given previous research on their socioeconomic gradients [29, 33–36]. The average SCAPIS participant seems to have higher HDL cholesterol and lower triglyceride levels, suggesting that lipid profiles may differ between SCAPIS participants and the target population. This result can potentially be explained, at least in part, by the negative effect of smoking on HDL [37] and the positive association between BMI and triglycerides [38].
Each of the risk factors listed above is associated with premature mortality and morbidity [39–45], and a meaningful imbalance between the sample and target population could therefore imply a risk of selection bias and lack of generalizability. Such biases depend on the causal pathway(s) between the sample selection mechanism, target parameter, and outcome(s) of interest (see, e.g., references [11, 13, 46] for details). While they, therefore, need to be evaluated before each analysis, our results may provide important clues as to which analyses may be more problematic than others. For instance, SCAPIS researchers may need to proceed with extra caution when analyzing associations between alcohol or smoking habits and cardiopulmonary outcomes.
Limitations
There are some limitations to our analyses that are important to keep in mind. Firstly, we can only account for selection due to the sociodemographic factors that we observed in our data, but study participation may also depend on other, unobserved factors. Secondly, we currently lack the prospective data required to fully assess the potential bias due to selective participation in associations between cardiopulmonary risk factors and prospective outcomes in SCAPIS. In general, the rich register infrastructures available in the Nordic countries allow for comprehensive investigations into the effects of selection [12, 15], which could be used to extend our analyses once sufficient prospective data become available.
Conclusions
The accuracy of the SCAPIS participation model was improved by combining individual and small area sociodemographic data. Reweighting the study participants based on this model led to more considerable changes in cardiopulmonary risk factor distributions than using either data source alone. Thus, combining individual and area-level data can potentially improve the assessment and handling of selective participation in cohort studies.
Supporting information
S1 Appendix. Supplementary tables, figures and mathematical derivations.
https://doi.org/10.1371/journal.pone.0265088.s001
(DOCX)
Acknowledgments
We thank the participants and investigators of SCAPIS for enabling this study. We are also grateful for the coordination and assistance provided by Sofia Swedenborg (Swedish Heart-Lung Foundation) to facilitate the writing of this paper.
Citation: Bonander C, Nilsson A, Björk J, Blomberg A, Engström G, Jernberg T, et al. (2022) The value of combining individual and small area sociodemographic data for assessing and handling selective participation in cohort studies: Evidence from the Swedish CardioPulmonary bioImage Study. PLoS ONE 17(3): e0265088. https://doi.org/10.1371/journal.pone.0265088
1. Westreich D, Edwards JK, Lesko CR, Cole SR, Stuart EA. Target Validity and the Hierarchy of Study Designs. Am J Epidemiol. 2019;188: 438–443. pmid:30299451
2. Bergström G, Berglund G, Blomberg A, Brandberg J, Engström G, Engvall J, et al. The Swedish CArdioPulmonary BioImage Study: objectives and design. J Intern Med. 2015;278: 645–659. pmid:26096600
3. Galea S, Tracy M. Participation rates in epidemiologic studies. Ann Epidemiol. 2007;17: 643–653. pmid:17553702
4. Silva Junior SHA da, Santos SM, Coeli CM, Carvalho MS. Assessment of participation bias in cohort studies: systematic review and meta-regression analysis. Cad Saude Publica. 2015;31: 2259–2274. pmid:26840808
5. Bergström G, Persson M, Adiels M, Björnson E, Bonander C, Ahlström H, et al. Prevalence of Subclinical Coronary Artery Atherosclerosis in the General Population. Circulation. 2021;144: 916–929. pmid:34543072
6. Björk J, Strömberg U, Rosengren A, Toren K, Fagerberg B, Grimby-Ekman A, et al. Predicting participation in the population-based Swedish cardiopulmonary bio-image study (SCAPIS) using register data. Scand J Public Health. 2017;45: 45–49. pmid:28683666
7. Hernán MA, Hernández-Díaz S, Robins JM. A structural approach to selection bias. Epidemiology. 2004;15: 615–625. pmid:15308962
8. Björk J, Nilsson A, Bonander C, Strömberg U. A novel framework for classification of selection processes in epidemiological research. BMC Medical Research Methodology. 2020;20: 155. pmid:32536343
9. Lesko CR, Ackerman B, Webster-Clark M, Edwards JK. Target Validity: Bringing Treatment of External Validity in Line with Internal Validity. Curr Epidemiol Rep. 2020;7: 117–124. pmid:33585162
10. Cole SR, Stuart EA. Generalizing evidence from randomized clinical trials to target populations: The ACTG 320 trial. Am J Epidemiol. 2010;172: 107–115. pmid:20547574
11. Pearl J, Bareinboim E. External Validity: From Do-Calculus to Transportability Across Populations. Statistical Science. 2014;29: 579–595.
12. Nilsson A, Bonander C, Strömberg U, Björk J. Can the validity of a cohort be improved by reweighting based on register data? Evidence from the Swedish MDC study. BMC Public Health. 2020;20: 1918. pmid:33334333
13. Nilsson A, Bonander C, Strömberg U, Björk J. A directed acyclic graph for interactions. Int J Epidemiol. 2021;50: 613–619. pmid:33221880
14. Bonander C, Nilsson A, Bergström GML, Björk J, Strömberg U. Correcting for selective participation in cohort studies using auxiliary register data without identification of non-participants. Scand J Public Health. 2019; 1403494819890784. pmid:31826719
15. Bonander C, Nilsson A, Björk J, Bergström GML, Strömberg U. Participation weighting based on sociodemographic register data improved external validity in a population-based cohort study. Journal of Clinical Epidemiology. 2019;108: 54–63. pmid:30562543
16. Elliott P, Savitz DA. Design Issues in Small-Area Studies of Environment and Health. Environ Health Perspect. 2008;116: 1098–1104. pmid:18709174
17. Hong J-L, Webster-Clark M, Jonsson Funk M, Stürmer T, Dempster SE, Cole SR, et al. Comparison of Methods to Generalize Randomized Clinical Trial Results Without Individual-Level Data for the Target Population. Am J Epidemiol. 2019;188: 426–437. pmid:30312378
18. Roux AVD, Mair C. Neighborhoods and health. Annals of the New York Academy of Sciences. 2010;1186: 125–145. pmid:20201871
19. Björk J, Berglund A, Härkönen J, Scott K. Practical and methodological issues in register-based research. Scand J Public Health. 2017;45: 3–4. pmid:28683664
20. Strömberg U, Baigi A, Holmén A, Parkes BL, Bonander C, Piel FB. A comparison of small-area deprivation indicators for public-health surveillance in Sweden. Scand J Public Health. 2021;In press, published online: July 20, 2021. pmid:34282665
21. Ludvigsson JF, Almqvist C, Bonamy A-KE, Ljung R, Michaëlsson K, Neovius M, et al. Registers of the Swedish total population and their use in medical research. Eur J Epidemiol. 2016;31: 125–136. pmid:26769609
22. Ludvigsson JF, Otterblad-Olausson P, Pettersson BU, Ekbom A. The Swedish personal identity number: possibilities and pitfalls in healthcare and medical research. Eur J Epidemiol. 2009;24: 659–667. pmid:19504049
23. Nilsson A, Bonander C, Strömberg U, Canivet C, Östergren P-O, Björk J. Reweighting a Swedish health questionnaire survey using extensive population register and self-reported data for assessing and improving the validity of longitudinal associations. PLOS ONE. 2021;16: e0253969. pmid:34197538
24. Austin PC, Stuart EA. Moving towards best practice when using inverse probability of treatment weighting (IPTW) using the propensity score to estimate causal treatment effects in observational studies. Statistics in Medicine. 2015;34: 3661–3679. pmid:26238958
25. Yang D, Dalton J. A unified approach to measuring the effect size between two groups using SAS. SAS Global Forum. 2012;335: 1–6.
26. Austin PC. Balance diagnostics for comparing the distribution of baseline covariates between treatment groups in propensity-score matched samples. Stat Med. 2009;28: 3083–3107. pmid:19757444
27. Steenland K, Henley J, Calle E, Thun M. Individual- and area-level socioeconomic status variables as predictors of mortality in a cohort of 179,383 persons. Am J Epidemiol. 2004;159: 1047–1056. pmid:15155289
28. Devaux M, Sassi F. Social disparities in hazardous alcohol use: self-report bias may lead to incorrect estimates. Eur J Public Health. 2016;26: 129–134. pmid:26585784
29. Roche A, Kostadinov V, Fischer J, Nicholas R, O’Rourke K, Pidd K, et al. Addressing inequities in alcohol consumption and related harms. Health Promotion International. 2015;30: ii20–ii35. pmid:26420810
30. Stamatakis E, Owen KB, Shepherd L, Drayton B, Hamer M, Bauman AE. Is Cohort Representativeness Passé? Poststratified Associations of Lifestyle Risk Factors with Mortality in the UK Biobank. Epidemiology. 2021;32: 179–188. pmid:33492009
31. Vartiainen E, Seppälä T, Lillsunde P, Puska P. Validation of self reported smoking by serum cotinine measurement in a community-based study. Journal of Epidemiology & Community Health. 2002;56: 167–170. pmid:11854334
32. Levey AS, Stevens LA, Schmid CH, Zhang Y (Lucy), Castro AF, Feldman HI, et al. A New Equation to Estimate Glomerular Filtration Rate. Ann Intern Med. 2009;150: 604–612. pmid:19414839
33. Al-Qaoud TM, Nitsch D, Wells J, Witte DR, Brunner EJ. Socioeconomic Status and Reduced Kidney Function in the Whitehall II Study: Role of Obesity and Metabolic Syndrome. Am J Kidney Dis. 2011;58: 389–397. pmid:21719176
34. Hiscock R, Bauld L, Amos A, Fidler JA, Munafò M. Socioeconomic status and smoking: a review. Annals of the New York Academy of Sciences. 2012;1248: 107–123. pmid:22092035
35. Norberg M, Lindvall K, Stenlund H, Lindahl B. The obesity epidemic slows among the middle-aged population in Sweden while the socioeconomic gap widens. Global Health Action. 2010;3: 5149. pmid:21160918
36. Hedlund U, Eriksson K, Rönmark E. Socio-economic status is related to incidence of asthma and respiratory symptoms in adults. Eur Respir J. 2006;28: 303–310. pmid:16540503
37. Forey BA, Fry JS, Lee PN, Thornton AJ, Coombs KJ. The effect of quitting smoking on HDL-cholesterol—a review based on within-subject changes. Biomark Res. 2013;1: 26. pmid:24252691
38. Shamai L, Lurix E, Shen M, Novaro GM, Szomstein S, Rosenthal R, et al. Association of body mass index and lipid profiles: evaluation of a broad spectrum of body mass index patients including the morbidly obese. Obes Surg. 2011;21: 42–47. pmid:20563664
39. Stringhini S, Carmeli C, Jokela M, Avendaño M, Muennig P, Guida F, et al. Socioeconomic status and the 25 × 25 risk factors as determinants of premature mortality: a multicohort study and meta-analysis of 1·7 million men and women. The Lancet. 2017;389: 1229–1237. pmid:28159391
40. Zhong G-C, Huang S-Q, Peng Y, Wan L, Wu Y-Q-L, Hu T-Y, et al. HDL-C is associated with mortality from all causes, cardiovascular disease and cancer in a J-shaped dose-response fashion: a pooled analysis of 37 prospective cohort studies. Eur J Prev Cardiolog. 2020;27: 1187–1203. pmid:32283957
41. Liu J, Zeng F-F, Liu Z-M, Zhang C-X, Ling W, Chen Y-M. Effects of blood triglycerides on cardiovascular and all-cause mortality: a systematic review and meta-analysis of 61 prospective studies. Lipids Health Dis. 2013;12: 159. pmid:24164719
42. Rehm J, Gmel G, Sempos CT, Trevisan M. Alcohol-Related Morbidity and Mortality. Alcohol Res Health. 2003;27: 39–51. pmid:15301399
43. Santos M, Kitzman DW, Matsushita K, Loehr L, Sueta CA, Shah AM. Prognostic Importance of Dyspnea for Cardiovascular Outcomes and Mortality in Persons without Prevalent Cardiopulmonary Disease: The Atherosclerosis Risk in Communities Study. PLOS ONE. 2016;11: e0165111. pmid:27780208
44. Abdelaal M, le Roux CW, Docherty NG. Morbidity and mortality associated with obesity. Ann Transl Med. 2017;5. pmid:28480197
45. Boriani G, Laroche C, Diemberger I, Popescu MI, Rasmussen LH, Petrescu L, et al. Glomerular filtration rate in patients with atrial fibrillation and 1-year outcomes. Scientific Reports. 2016;6: 30271. pmid:27466080
46. Biele G, Gustavson K, Czajkowski NO, Nilsen RM, Reichborn-Kjennerud T, Magnus PM, et al. Bias from self selection and loss to follow-up in prospective cohort studies. Eur J Epidemiol. 2019;34: 927–938. pmid:31451995
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
© 2022 Bonander et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Abstract
Objectives
To study the value of combining individual- and neighborhood-level sociodemographic data to predict study participation and assess the effects of baseline selection on the distribution of metabolic risk factors and lifestyle factors in the Swedish CardioPulmonary bioImage Study (SCAPIS).
Methods
We linked sociodemographic register data to SCAPIS participants (n = 30,154, ages: 50–64 years) and a random sample of the study’s target population (n = 59,909). We assessed the classification ability of participation models based on individual-level data, neighborhood-level data, and combinations of both. Standardized mean differences (SMD) were used to examine how reweighting the sample to match the population affected the averages of 32 cardiopulmonary risk factors at baseline. Absolute SMDs >0.10 were considered meaningful.
Results
Combining both individual-level and neighborhood-level data gave rise to a model with better classification ability (AUC: 71.3%) than models with only individual-level (AUC: 66.9%) or neighborhood-level data (AUC: 65.5%). We observed a greater change in the distribution of risk factors when we reweighted the participants using both individual and area data. The only meaningful change was related to the (self-reported) frequency of alcohol consumption, which appears to be higher in the SCAPIS sample than in the population. The remaining risk factors did not change meaningfully.
Conclusions
Both individual- and neighborhood-level characteristics are informative in assessing study selection effects. Future analyses of cardiopulmonary outcomes in the SCAPIS cohort can benefit from our study, though the average impact of selection on risk factor distributions at baseline appears small.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer