Partners:
Jena, Germany
London, UK
Utrecht, Netherlands
Amsterdam, Netherlands
Barcelona, Spain
Bonn, Germany
Heidelberg, Germany
Szeged, Hungary
Zurich, Switzerland
Marie Curie Action:
035987
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Normative Study of Healthy Twin Pairs
We have carried out a sufficiently representative study of healthy twins in order to
systematically investigate the issue of within-pair concordance in monozygotic (mz)
and dizygotic (dz) twins [Lykken and Stassen: data of 1,300 dz and 1,434 mz twin pairs].
By definition, the genetic similarity between mz co-twins is "1" and that of dz
co-twins "0.5". On the phenotype level, however, the concordance of mz and dz co-twins
follows a normal distribution with mean values and variances ("norm of reaction").
In particular, the dz concordance can vary from complete dissimilarity (comparable
unrelated individuals) and perfect similarity (comparable to mz co-twins). The analysis
of quantitative traits "finger ridge count", "body height", "brain-wave patterns",
"shoe size", and "body weight" yield almost perfect mz:dz ratios of 2:1, thus suggesting
an additive genetic model in the background (Table). In that case the mz concordance
gives the size of the genetic backgound (e.g., 82% of the observed inter-individual
variance of barinwave patterns is explainable by genetic factors). Significant
deviations from the 2:1 ratio indicate a more complex interplay between environment
and genetic factors. For example, several IQ dimensions display the same high
concordances for dz and mz co-twins, thus suggesting dominant environmental factors.
Quantitative Syndrome-Oriented Approaches to Psychopathology
Major psychiatric disorders are familial in the sense that they "run" in families but
they do not seggregate. In fact, the underlying vulnerability acts unspecificly
and is neither a necessary nor a sufficient condition for developing a psychiatric
disorder or a particular clinical diagnosis. The phenotypical picture is not
homotypic in terms of clinical diagnoses, for example, we frequently observe first
degree relatives with a diagnosis of depression in families ascetrained through index
cases with a diagnosis of schizophrenia. Quantitative syndrome-oriented approaches
apparently offer advantages over the qualitative taxonomy of diagnostic systems.
Specifically, multidimensional syndrome patterns have turned out (1) to resolve the
fine gradations of within-family psychopathologies that do not reach diagnostic
thresholds, and (2) to relate to the time course of recovery under psychotropic drug
treatment.
Twins with Schizophrenia
Quantitative sychopathology syndrome scores suggest that mz
co-twins who shared the same environment have a 3.7-fold higher risk to both suffer
from schizophrenic disorders, compared to dz co-twins raised together (Table).
Significant deviations from the mz:dz ratio of 2:1 indicate the existence of strong
non-linearities which are typical for self-regulating systems, such as the monoaminergic
systems or the inflammatory response system. In fact, there is evidence that mz co-twins
concordant for schizophrenia may possess a less "robust" variant of the inflammatory
response system that can more easily be triggered by exogenous factors compared to the
more "robust" variants postulated for mz co-twins discordant for schizophrenia.
Moreover, data from 753 patients under antidepressants or antipsychotics suggest that
up to 15% of the response to antidepressants and up to 25% of the response to
antipsychotics might be explainable through the inflammatory response system.
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Within-pair concordances of psychopathology syndrome scores in mz and dz twins where
at least one co-twin suffers from schizophrenic disorder. No more than 55% of mz and 15% of
dz co-twins are concordant for schizophrenia, thus displaying significant deviations
from the mz:dz ratio of 2:1.
Detailed analyses of our family data showed that: (1) patients with a clinical diagnosis of
schizoaffective disorders have the highest genetic vulnerability; (2) the genetic vulnerability
depends on the age of onset and the severity of psychopathology scores;
(3) genetic vulnerability appears to be ethnicity-independent.
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