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IPS254 Thaddeus Tarpey et al.
               For  the  diagnosis  of  autism  spectrum  disorder  (ASD),  the  debate  has
            centered  on  whether  distinct  disease  categories  exist  or  is  there  is  an
            underlying “spectrum”  of  disease severity that includes for example ADHD
            (Grzadzinski et al., 2011). This issue was the focus of a recent article Kim et al.
            (2018) that proposes that ASD consists of three spectrums instead of a single
            spectrum. Their statistical analysis that led them to conclude ASD consists fo
            three spectrums was based on Latent Class Factor Analysis (LCFA). The LCFA
            incorporates both categorical features for presumed latent classes as well as
            “dimensional”  features  corresponding  to  within  group  continuous  latent
            factors. Their statistical strategy in determining an appropriate model to use
            was  to  build  up  the  model  starting  with  only  two  latent  classes  and  one
            continuous factor per group and then increase the number of classes and
            factors per class.
               Another avenue of discovery in the context of psychiatric nosology is to
            incorporate  information  of  defining  diagnosis  categories  not  only  on
            symptoms but also on treatment outcome. Of course, a  problem with this
            approach is that the type of treatment usually depends on diagnosis. However,
            many psychiatric illnesses are treated with the same types of medications.
               A  major  statistical  challenge  for  this  work  is  the  issue  of  aliasing.  For
            psychiatric nosology, finite mixtures of normal distributions are an attractive
            approach to the unsupervised learning problem of estimating parameters for
            discrete disease populations. However, it has long been recognized that finite
            mixture  distributions  are  often  indistinguishable  from  homogenous
            continuous distributions (Pearson, 1895). If the components of the mixture
            distribution are normal, then the model is identifiable (e.g., Teicher, 1961). If
            distinct populations do not exist and disease severity varies continuously, then
            one can use an infinite mixture of normals which is also identifiable under
            certain conditions (Bruni and Koch, 1985). If it is believed there are distinct
            disease categories, then from a statistical point of view, this problem can be
            cast  in  the  context  of  unsupervised  learning  and  finite  mixture  model
            approaches may be suitable. However, if distinct disease classes do not exist,
            and disease severity varies continuously along a spectrum, then an infinite
            mixture  model  may  be  a  more  appropriate  statistical  approach  to  the
            psychiatric  nosology  problem.  For  example,  Tarpey  and  Petkova  (2010)
            proposed an infinite mixture model in the context of a simple regression where
            the  predictor  variable  is  continuous  and  latent.  If  the  latent  predictor  is
            Bernoulli, then the regression model becomes a 2-component finite mixture
            model. Tarpey and Petkova (2010) considered a predictor variable that has a
            beta distribution whereby in the limiting cases, the beta can converge to a
            Bernoulli. In this way, the 2-component mixture and infinite mixture can be
            described in a single model. Tarpey and Petkova (2010) introduced this model
            in order to model placebo response when treating depression.

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