Peter,
Many thanks for your prompt reply.
I think you may have been too quick to dismiss model2; there is no need for
time to be negative. The time parameter is Surv represents survival, i.e.
follow-up time. We usually start the follow-up clock at the time a subject is
enrolled into a study, but this is not the only measure of survival time. One
might argue that the clock should start at birth because the subject has
survived to birth to plus the time represented by the ususal follow-up clock.
John
John Sorkin M.D., Ph.D.
Chief, Biostatistics and Informatics
Baltimore VA Medical Center GRECC,
University of Maryland School of Medicine Claude D. Pepper OAIC,
University of Maryland Clinical Nutrition Research Unit, and
Baltimore VA Center Stroke of Excellence
University of Maryland School of Medicine
Division of Gerontology
Baltimore VA Medical Center
10 North Greene Street
GRECC (BT/18/GR)
Baltimore, MD 21201-1524
(Phone) 410-605-7119
(Fax) 410-605-7913 (Please call phone number above prior to faxing)
[EMAIL PROTECTED]
>>> Peter Dalgaard <[EMAIL PROTECTED]> 2/5/2007 9:16 AM >>>
John Sorkin wrote:
> I hope one and all will allow a stats question:
>
> When running a cox proportional hazards model ,there are two ways to
> deal with age,
> including age as a covariate, or to include age as part of the
> follow-up time, viz,
>
> Age as a covariate:
>
> tetest1 <- list(time= c(4, 3,1,1,2,2,3),
> status=c(1,NA,1,0,1,1,0),
> age= c(0, 2,1,1,1,0,0),
> riskfactor= c(0, 0,0,0,1,1,1))
> fitagecovariate<-coxph( Surv(time, status) ~ age +riskfactor, test1)
> fitagecovariate
>
> Age included as part of follow-up time:
>
> test2<-test1
> test2$timeplusage<-test2$time+test2$age
> fitagefollowup<-coxph( Surv(timeplusage, status) ~ riskfactor, test2)
> fitagefollowup
>
> I would appreciate any thoughts about the differences in the
> interpretation of the two models.
> One obvious difference is that in the first model (fitagecovariate) one
> can make inferences about age and in the second one cannot. I think a
> second
> difference may be that in the first model the riskfactor is assumed to
> have values measured at the values of age where as in the second model
> riskfactor is assumed to have given values throughout the subject's
> life.
>
>
Model2 is plainly wrong, unless your times can be negative it represents
long stretches of immortality (more obvious if all ages are about
80...)! Presumably, age is the age at entry, so a delayed-entry model
could be appropriate (Surv(age,timeplusage,status)). If this
modification is made, the main difference is that the time-since-entry
scale can not (easily) have a separate effect in the delayed-entry
model. If time is really is time since diagnosis or operation, then that
could be badly wrong.
> Your thoughts please.
>
> Thanks,
> John
>
> R 2.1.1
> windows XP
>
> John Sorkin M.D., Ph.D.
> Chief, Biostatistics and Informatics
> Baltimore VA Medical Center GRECC,
> University of Maryland School of Medicine Claude D. Pepper OAIC,
> University of Maryland Clinical Nutrition Research Unit, and
> Baltimore VA Center Stroke of Excellence
>
> University of Maryland School of Medicine
> Division of Gerontology
> Baltimore VA Medical Center
> 10 North Greene Street
> GRECC (BT/18/GR)
> Baltimore, MD 21201-1524
>
> (Phone) 410-605-7119
> (Fax) 410-605-7913 (Please call phone number above prior to faxing)
> [EMAIL PROTECTED]
>
> Confidentiality Statement:
> This email message, including any attachments, is for the so...{{dropped}}
>
> ______________________________________________
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> and provide commented, minimal, self-contained, reproducible code.
>
--
O__ ---- Peter Dalgaard Ă˜ster Farimagsgade 5, Entr.B
c/ /'_ --- Dept. of Biostatistics PO Box 2099, 1014 Cph. K
(*) \(*) -- University of Copenhagen Denmark Ph: (+45) 35327918
~~~~~~~~~~ - ([EMAIL PROTECTED]) FAX: (+45) 35327907
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