1 / 42

Multilevel Analysis

Multilevel Analysis. Kate Pickett Senior Lecturer in Epidemiology. Perspective. Health researchers: Are interested in answering research questions (not maths) Want to be able to apply statistical techniques Want to be able to interpret results

Télécharger la présentation

Multilevel Analysis

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Multilevel Analysis Kate Pickett Senior Lecturer in Epidemiology

  2. Perspective • Health researchers: • Are interested in answering research questions (not maths) • Want to be able to apply statistical techniques • Want to be able to interpret results • Want to be able to communicate with consumers and statisticians

  3. Aims for this session • Understand the rationale for multilevel analysis • Understand common terminology • Interpret output from multilevel models • Be able to read and critically appraise studies using multilevel models

  4. Context and composition • Studying populations (groups) and individuals From Rose, G. Sick individuals and sick populations. Int J Epidemiol 1985;14:32-38

  5. Levels of analysis • Health researchers may collect and use data collected at the level of: • Individuals, patients • Families or other social groupings • Clinics or hospitals • Small areas, neighbourhoods • Large populations

  6. Population A Population B How is Population A different from Population B?

  7. Ecological studies • Data are aggregated and represent a group, rather than an individual • incidence rate of an illness • prevalence of a particular health service • We don’t know which particular individuals within the group were ill or received the service • These group-based outcome measures are analyzed by correlating them with determinants measured for the same groups

  8. Source: Pickett KE, Kelly S, Brunner E, Lobstein T, Wilkinson RG. Wider income gaps, wider waistbands? An ecological study of obesity and income inequality. J Epidemiol Community Health 2005;59:670–674.

  9. The ecological fallacy • Associations at the group level may not hold at an individual level • Eg, we might see that rates of obesity are correlated internationally with per capita calorie intake • But, we don’t know if it is the obese individuals who are eating all the calories • Many group-level variables are correlated so we may get spurious correlations • Eg, obesity rates may also be correlated with number of zoos per capita or some other completely unrelated factor

  10. The atomistic fallacy • But the ecological fallacy has a flip side • Factors that affect outcomes in individuals may not operate in the same way at the population level • Eg, teenage births are more common among the poor, but teenage birth rates are very high in some very wealthy countries.

  11. Example of teenage births Source: Pickett KE, Mookherjee S, Wilkinson RG. Adolescent Birth Rates,Total Homicides, and Income Inequality In Rich Countries, AJPH 2005;95:1181-1183.

  12. Sometimes ecological studies are done because it is quick and easy Sometimes ecological studies are the best design for the research question BECAUSE Some determinants are “ecological”: Population density Air quality/pollution GNP Income inequality % unemployed Ambient temperature Ecological variables

  13. Context and composition • But what if we are interested in both types of variables (individual and population) simultaneously? • Eg: we might want to know about the effect of population-level unemployment on health, above and beyond the health impact of being unemployed for any given individual

  14. Multilevel models

  15. Introduction to multilevel models • Hierarchical models • Mixed effects models • Random effects models

  16. Developed in education research Observations of students in a single class are not independent of one another “Standard” statistical models assume that observations are independent Two-level hierarchy Students within classes Three-level hierarchy Students within classes within schools Four-level hierarchy Students within classes within schools within local authority areas Background

  17. Health research context • Patients within a medical practice • Residents within neighbourhoods • Subjects within trial clusters • Hospitals within PCTs….

  18. Examples for class • Some examples are drawn from Twisk JWR “Applied Multilevel Analysis” Cambridge University Press, 2006 • Example data are available at: http:\www.emgo.nl\researchtools • Research question: what is the relationship between total cholesterol and age? • Statistical software: Stata but note that MLwiN is free to UK academics: http://www.cmm.bristol.ac.uk/MLwiN/download/index.shtml)

  19. Simple linear regression Total cholesterol = β0 + β1 x age + ε

  20. Simple linear regression, adding a categorical variable Total cholesterol = β0 + β1 x age + β2 x gender +ε

  21. Simple linear regression, adding another variable (doctor) Total cholesterol = β0 + β1 x age + β2 x MD1 + β3 x MD2+ β4 x MD3+ β5 x MD4+…..+ βm x MDm-1+ ε

  22. Multilevel analysis • Instead of estimating all those separate intercepts, we estimate the variance of them • In our example that means estimating 1 additional parameter, rather than 11 • We are allowing the intercept to be random (random effects modelling) • An efficient way of correcting for a variable with many categories • Trade-off: • Assumes that the different intercepts are normally distributed

  23. Example data Cholesterol Dataset • 441 patients • Age 44-86 years • Cholesterol 3.90-8.86 mmol/l • 12 doctors

  24. Non-multilevel regression . regress cholesterol age Source | SS df MS Number of obs = 441 -------------+------------------------------ F( 1, 439) = 142.06 Model | 99.3395851 1 99.3395851 Prob > F = 0.0000 Residual | 306.984057 439 .699280312 R-squared = 0.2445 -------------+------------------------------ Adj R-squared = 0.2428 Total | 406.323642 440 .923462822 Root MSE = .83623 ------------------------------------------------------------------------------ cholesterol | Coef. Std. Err. t P>|t| [95% Conf. Interval] -------------+---------------------------------------------------------------- age | .0512619 .0043009 11.92 0.000 .042809 .0597148 _cons | 2.798691 .268571 10.42 0.000 2.270847 3.326536 ------------------------------------------------------------------------------ Example using Stata

  25. . xtmixed cholesterol age ||doctor:, ml var Performing EM optimization: Performing gradient-based optimization: Iteration 0: log likelihood = -404.68939 Iteration 1: log likelihood = -404.68939 Computing standard errors: Mixed-effects ML regression Number of obs = 441 Group variable: doctor Number of groups = 12 Obs per group: min = 36 avg = 36.8 max = 39 Wald chi2(1) = 262.76 Log likelihood = -404.68939 Prob > chi2 = 0.0000 ------------------------------------------------------------------------------ cholesterol | Coef. Std. Err. z P>|z| [95% Conf. Interval] -------------+---------------------------------------------------------------- age | .0495866 .003059 16.21 0.000 .0435911 .0555822 _cons | 2.905812 .259134 11.21 0.000 2.397919 3.413705 ------------------------------------------------------------------------------ ------------------------------------------------------------------------------ Random-effects Parameters | Estimate Std. Err. [95% Conf. Interval] -----------------------------+------------------------------------------------ doctor: Identity | var(_cons) | .3685781 .1541985 .1623381 .8368327 -----------------------------+------------------------------------------------ var(Residual) | .3314923 .0226341 .2899706 .3789597 ------------------------------------------------------------------------------ LR test vs. linear regression: chibar2(01) = 282.37 Prob >= chibar2 = 0.0000 Multilevel Model in Stata

  26. Do we need the multilevel model? • Likelihood ratio test: • Compare -2 log likelihood of model with random intercept to -2 log likelihood of ordinary linear model • Difference has a Chi-square distribution with df = difference in number of parameters estimated • Difference = 284.73, highly significant

  27. Model parameters • Effects of age in each model: • Coefficient in ordinary model = 0.0513 • Coefficient in multilevel model = 0.0496 • 95% CI in ordinary model (0.0428, 0.0597) • 95% CI in multilevel model (0.0435,0.0556) • Age is significant in both models

  28. Intraclass correlation coefficient • This measures how dependent the observations are within clusters • Eg, how correlated are the observations of patients belonging to the same doctor? • Defined as: • Variance between clusters/Total variance • The smaller the variance within clusters, the greater the ICC

  29. ICC (a) Distribution of an outcome variable Assume that the total variance = 10

  30. ICC (b) ICC is low because: Variance within groups is high (9) Variance between groups is low (1) Numerator is small, relative to denominator ICC = 1/10=0.1

  31. ICC (c) The groups are now more spread out, more different, and: ICC is bigger because: Variance within groups is lower (5) Variance between groups is higher (5) ICC=5/10 = 0.5

  32. ICC (d) The groups are now completely different, and: ICC is maximised because: Variance within groups is minimal (1) Variance between groups is maximal (9) Numerator is large, relative to denominator ICC=9/10 = 0.9 MUCH MORE DEPENDENCE WITHIN CLUSTER – each observation provides less unique information

  33. Impact on significance tests Table of alpha values under different conditions of sample size and ICC

  34. ICC in our example • ICC = between doctor variance/total variance • ICC = 0.3686/(0.3686+0.3315) = 0.3686/0.7001 = 0.526 52.6% of the total individual differences in cholesterol are at the doctor level

  35. ICC • When ICC is high • Evidence of a contextual effect on the outcome • Evidence of differences in composition between the clusters • Explore by including explanatory variables at each level • When ICC is low • No need for a multilevel analysis

  36. Back to unemployment example

  37. Data Structure Population B Population A Red = unemployed

  38. An ordinary regression model Health =b0 + b1 (unemployed) + b2 (% unemployed) + e e represents the effect of all omitted variables and measurement error and is assumed to have a random effect (so it gets ignored)

  39. Data Structure Population B Population A Aside from unemployment, subjects in A are different from B in other ways: composition (shape, size), context (density)

  40. A multi-level regression model i = individual, j=context: yij = bxij + BXi + Ej + eij Health = b (unemployedij) + B(% unemployedi) +Ej + eij

  41. When data are hierarchical or multi-level by nature, they should be analysed appropriately The coefficients or odds ratios from the models can be interpreted as usual The ICC shows how much variance in the outcome occurs between the higher-level contexts If appropriate methods are not used, standard errors and significance tests may be wrong and coefficients biased What does this mean for critical appraisal of the health literature?

  42. A summary • Ecological studies • Appropriate when the research question concerns only ecological effects • Ecological fallacy may be a problem • Individual-level studies • Appropriate when the research question concerns only individual-level effects • Atomistic fallacy may be a problem • Multi-level studies • Appropriate when the research question concerns both context and composition of populations

More Related