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Re: st: Thinking through best way to do a longitudinal analysis

From   Austin Nichols <>
Subject   Re: st: Thinking through best way to do a longitudinal analysis
Date   Sun, 16 Aug 2009 18:02:38 -0400

Chelsea <> :
You can use -statsby- or just calculate directly using a loop over
individuals with -foreach- or using time series operators and the
formula for regression.  But why do you think a linear trend is
appropriate?  Or are you planning to transform the depvar first?  More
importantly, why do you want the individual trends?  Start with
-xtmixed- regressions of the depvar on a spline in time interacted
with the dummy for contraception.  But contraception is not
exogenous--do you have some strategy for causal inference?  I.e. how
do you know any observed difference is the result of contraception
versus some other characteristic associated with contraception?

On Sun, Aug 16, 2009 at 4:23 PM, Polis, Chelsea B.<> wrote:
> Thanks so much to both of you for the suggestions and all of these great references!  I will download all of these articles and read them.  In the meantime, do you think calculating individual slopes is a bad idea?  If not, do you know how I might go about doing this in STATA?
> Thank you!
> Chelsea
> -----Original Message-----
> From: [] On Behalf Of Cameron McIntosh
> Sent: Friday, August 14, 2009 10:36 PM
> Subject: RE: st: Thinking through best way to do a longitudinal analysis
> Chelsea,
> I'll try and point you in what I think might be a good direction. You may want to read up on growth mixture modeling:
> Wang, M., & Bodner, T.E. (2007). Growth Mixture Modeling: Identifying and Predicting Unobserved Subpopulations With Longitudinal Data. Organizational Research Methods, 10(4), 635-656.
> Dolan, C.V., Schmittmann, V.D., Lubke, G.H. & Neale, M.C. (2005). Regime switching in the latent growth curve mixture model. Structural Equation Modeling, 12, 94-119
> Muthén, B.O. (2004). Latent variable analysis: Growth mixture modeling and related techniques for longitudinal data. In D.Kaplan (Ed.), Handbook of quantitative methodology for the social sciences (pp. 345-368). Newbury Park, CA: Sage.
> In this case you "know" your "latent classes" (hormonal contraception or not), but that's no problem. The varying assessment times and missing data could be a bit tricky but there is some literature out there:
> Blozis, S.A., & Cho, Y.I. (2008). Coding and centering of time in latent curve models in the presence of interindividual time heterogeneity. Structural Equation Modeling, 15(3), 413-433.
> Biesanz. J.C., Deeb-Sossa, N., Papadakis, A.A., Bollen, K.A., Curran, P..J. (2004). The role of coding time in estimating and interpreting growth curve models. Psychological Methods, 9(1), 30-52.
> Duncan, S.C., & Duncan, T.E. (1994). Modeling incomplete longitudinal substance use data using latent variable growth curve methodology. Multivariate Behavioral Research, 29(4), 313-338.
> -gllamm- might be able to do what you want (if not, Mplus for sure). Hope this is helpful,
> Cam
> ----------------------------------------
>> Date: Fri, 14 Aug 2009 13:27:15 -0700
>> From:
>> Subject: Re: st: Thinking through best way to do a longitudinal analysis
>> To:
>> Another option is to use a linear mixed model approach.
>> Scott Millis
>> --- On Fri, 8/14/09, Polis, Chelsea B.  wrote:
>>> From: Polis, Chelsea B.
>>> Subject: st: Thinking through best way to do a longitudinal analysis
>>> To: ""
>>> Date: Friday, August 14, 2009, 2:38 PM
>>> I am trying to do an analysis on the
>>> CD4 decline trajectory of 190 HIV+ women, comparing
>>> those who were on hormonal contraception around the time of
>>> HIV seroconversion against those
>>> who weren't.  Each subject in my sample has at least
>>> two (and as many as six) CD4 measurements,
>>> the first and the last of which include a time span of at
>>> least one year.  I created a
>>> variable to anchor the CD4 measurements in time by
>>> generating a variable that indicates how
>>> many days since HIV seroconversion the CD4 measurement was
>>> taken.  The data are not balanced
>>> (since women have anywhere between 2 to 6 measurements) and
>>> CD4 counts were not measured for
>>> each individual at the same point in time after
>>> seroconversion (for example, the first measurement
>>> available for each woman ranges in days since
>>> seroconversion from 69 to 1919).
>>> I think one way to go about this would be to calculate the
>>> individual slope for each subject and
>>> compare the slopes between contraceptive users and
>>> non-users using a t-test.  Is there a command
>>> to obtain those kind of individual regression slopes for
>>> each woman, and would my data have to be
>>> in long or wide format?
>>> Or am I thinking about this improperly?  Would it be
>>> better to construct a longitudinal marginal
>>> model with generalized estimating equations, and if so, can
>>> someone point me in the direction of
>>> a text that might help me figure out how to do that with
>>> what I think is probably an unusual data
>>> structure (many of the examples I have seen in coursework
>>> use data measured at regular intervals)?
>>> Many thanks,
>>> Chelsea

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