[R] BMA, logistic regression, odds ratio, model reduction etc

Frank Harrell f.harrell at vanderbilt.edu
Wed Apr 20 15:01:11 CEST 2011


Deleting variables is a bad idea unless you make that a formal part of the
BMA so that the attempt to delete variables is penalized for.  Instead of
BMA I recommend simple penalized maximum likelihood estimation (see the lrm
function in the rms package) or pre-modeling data reduction that is blinded
to the outcome variable.
Frank


細田弘吉 wrote:
> 
> Hi everybody,
> I apologize for long mail in advance.
> 
> I have data of 104 patients, which consists of 15 explanatory variables
> and one binary outcome (poor/good). The outcome consists of 25 poor
> results and 79 good results. I tried to analyze the data with logistic
> regression. However, the 15 variables and 25 events means events per
> variable (EPV) is much less than 10 (rule of thumb). Therefore, I used R
> package, "BMA" to perform logistic regression with BMA to avoid this
> problem.
> 
> model 1 (full model):
> x1, x2, x3, x4 are continuous variables and others are binary data.
> 
>> x16.bic.glm <- bic.glm(outcome ~ ., data=x16.df,
> glm.family="binomial", OR20, strict=FALSE)
>> summary(x16.bic.glm)
> (The output below has been cut off at the right edge to save space)
> 
>   62  models were selected
>  Best  5  models (cumulative posterior probability =  0.3606 ):
> 
>                          p!=0    EV         SD        model 1    model2
> Intercept                100    -5.1348545  1.652424    -4.4688  -5.15
> -5.1536
> age                        3.3   0.0001634  0.007258      .
> sex                        4.0
>    .M                           -0.0243145  0.220314      .
> side                      10.8
>     .R                           0.0811227  0.301233      .
> procedure                 46.9  -0.5356894  0.685148      .      -1.163
> symptom                    3.8  -0.0099438  0.129690      .          .
> stenosis                   3.4  -0.0003343  0.005254      .
> x1                        3.7  -0.0061451  0.144084      .
> x2                       100.0   3.1707661  0.892034     3.2221     3.11
> x3                        51.3  -0.4577885  0.551466    -0.9154     .
> HT                         4.6
>   .positive                      0.0199299  0.161769      .          .
> DM                         3.3
>   .positive                     -0.0019986  0.105910      .          .
> IHD                        3.5
>    .positive                     0.0077626  0.122593      .          .
> smoking                    9.1
>        .positive                 0.0611779  0.258402      .          .
> hyperlipidemia            16.0
>               .positive          0.1784293  0.512058      .          .
> x4                         8.2   0.0607398  0.267501      .          .
> 
> 
> nVar                                                       2          2
>          1          3          3
> BIC                                                   -376.9082
> -376.5588  -376.3094  -375.8468  -374.5582
> post prob                                                0.104
> 0.087      0.077      0.061      0.032
> 
> [Question 1]
> Is it O.K to calculate odds ratio and its 95% confidence interval from
> "EV" (posterior distribution mean) and“SD”(posterior distribution
> standard deviation)?
> For example, 95%CI of EV of x2 can be calculated as;
>> exp(3.1707661)
> [1] 23.82573     -----> odds ratio
>> exp(3.1707661+1.96*0.892034)
> [1] 136.8866
>> exp(3.1707661-1.96*0.892034)
> [1] 4.146976
> ------------------> 95%CI (4.1 to 136.9)
> Is this O.K.?
> 
> [Question 2]
> Is it permissible to delete variables with small value of "p!=0" and
> "EV", such as age (3.3% and 0.0001634) to reduce the number of
> explanatory variables and reconstruct new model without those variables
> for new session of BMA?
> 
> model 2 (reduced model):
> I used R package, "pvclust", to reduce the model. The result suggested
> x1, x2 and x4 belonged to the same cluster, so I picked up only x2.
> Based on the subject knowledge, I made a simple unweighted sum, by
> counting the number of clinical features. For 9 features (sex, side,
> HT2, hyperlipidemia, DM, IHD, smoking, symptom, age), the sum ranges
> from 0 to 9. This score was defined as ClinicalScore. Consequently, I
> made up new data set (x6.df), which consists of 5 variables (stenosis,
> x2, x3, procedure, and ClinicalScore) and one binary outcome
> (poor/good). Then, for alternative BMA session...
> 
>> BMAx6.glm <- bic.glm(postopDWI_HI ~ ., data=x6.df,
> glm.family="binomial", OR=20, strict=FALSE)
>> summary(BMAx6.glm)
> (The output below has been cut off at the right edge to save space)
> Call:
> bic.glm.formula(f = postopDWI_HI ~ ., data = x6.df, glm.family =
> "binomial",     strict = FALSE, OR = 20)
> 
> 
>   13  models were selected
>  Best  5  models (cumulative posterior probability =  0.7626 ):
> 
>                 p!=0    EV         SD       model 1    model 2
> Intercept       100    -5.6918362  1.81220    -4.4688    -6.3166
> stenosis          8.1  -0.0008417  0.00815      .          .
> x2              100.0   3.0606165  0.87765     3.2221     3.1154
> x3               46.5  -0.3998864  0.52688    -0.9154      .
> procedure       49.3   0.5747013  0.70164      .         1.1631
> ClinicalScore   27.1   0.0966633  0.19645      .          .
> 
> 
> nVar                                             2          2          1
>          3          3
> BIC                                         -376.9082  -376.5588
> -376.3094  -375.8468  -375.5025
> post prob                                      0.208      0.175
> 0.154      0.122      0.103
> 
> [Question 3]
> Am I doing it correctly or not?
> I mean this kind of model reduction is permissible for BMA?
> 
> [Question 4]
> I still have 5 variables, which violates the rule of thumb, "EPV > 10".
> Is it permissible to delete "stenosis" variable because of small value
> of "EV"? Or is it O.K. because this is BMA?
> 
> Sorry for long post.
> 
> I appreciate your help very much in advance.
> 
> --
> KH
> 
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> and provide commented, minimal, self-contained, reproducible code.
> 


-----
Frank Harrell
Department of Biostatistics, Vanderbilt University
--
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