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Structural Equation Modeling

1. Structural equation modeling (SEM) involves creating models of connectivity between brain regions activated during a task and testing how well these models fit experimental data. SEM analyzes the covariance between observations from different brain regions. 2. An example SEM model with 4 brain regions (A, B, C, D) and connections between them is shown. The path coefficients estimated by SEM represent effective connectivity between regions. 3. Models are evaluated based on goodness-of-fit criteria like chi-square, GFI, and RMSEA values, with better fitting models having smaller values. Differences in path coefficients between models can indicate qualitative or quantitative changes in connectivity between conditions.

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0% found this document useful (0 votes)
106 views14 pages

Structural Equation Modeling

1. Structural equation modeling (SEM) involves creating models of connectivity between brain regions activated during a task and testing how well these models fit experimental data. SEM analyzes the covariance between observations from different brain regions. 2. An example SEM model with 4 brain regions (A, B, C, D) and connections between them is shown. The path coefficients estimated by SEM represent effective connectivity between regions. 3. Models are evaluated based on goodness-of-fit criteria like chi-square, GFI, and RMSEA values, with better fitting models having smaller values. Differences in path coefficients between models can indicate qualitative or quantitative changes in connectivity between conditions.

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Ferra Yanuar
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1.

Structural Equation Modeling


Roughly speaking, SEM involves creation of possible connectivity models involving brain regions that are active for a given task, then testing the goodness of fit of these models to see if they can account for a significant amount of the experimental data. Here we use this technique to investigate possible connections between cortical regions that are active during processing of visual and audio-visual speech stimuli in both normal hearing and congenitally deaf individuals. SEM is a multivariate technique used to analyze the covariance of observations (McIntosh et al., 1996). When applying SEM techniques, one also has to find a compromise between model complexity, anatomical accuracy and interpretability since there are mathematical constraints that impose limits to how complex the model can be. The first step in the analysis is to define an anatomical model (constraining model), and the next step is to use the interregional covariances of activity to estimate the parameters of the model.

A x v
w

y D

Figure 1 Example of a structural model

Consider a simple example above in Figure 1 (from McIntosh and Gonzalez-Lima, 1994). Here, A, B, C and D represent the brain areas and the arrows labeled v, w, x, y, and z represent the anatomical connections. These together comprise the anatomical model for structural equation modeling analyses. In most cases, the time-series for each region A, B, C and D are extracted from the imaging data (fMRI data), and are normalized to zero mean and unit variance. Then the covariance matrices are computed on the basis of this time-series or observations obtained from these regions. The values for v, w, x, y, and z are calculated through a series of algebraic manipulations and are known as the path coefficients. These path coefficients (or connection strengths) are the parameters of the model, and these represent the estimates of effective connectivity. Essentially, the parameters of the model are estimated by minimizing the difference between the observed covariances and the covariances implied by the anatomical structural model. Mathematically, the above model can be written as a set of structural equations as:

A = A B = vA + B C = xA + wB + c D = yB + zC + D
For these equations, A, B, C and D are the known variables (measured covariances); v, w, x, y, and z are the unknown variables. For each region, a separate variable is included, and these represent the residual influences. Simply stated, this variable can be interpreted as the combined influences of areas outside the model and the influence of a brain region upon itself (McIntosh and Gonzalez-Lima, 1992). The path coefficients are normally computed using software packages such as AMOS, LISREL, and MX32. The starting values of the estimates are initially obtained using two-stage least squares, and they are iteratively modified using a maximum likelihood fit function (Joreskog and Sorbom, 1989). Minimizing the differences between observed and implied covariances is usually done with steepest-descent iterations. The structural equation modeling technique differs from other statistical approaches such as multiple regression or ANOVA where the regression coefficients are obtained from minimizing the sum squared differences between the predicted and observed dependent variables. In structural equation modeling, instead of considering individual observations (or variables) as with other usual statistical approaches, the covariance structure is emphasized. In the context of neural systems, the covariance measure corresponds to how much the neural activities of two or more brain regions are related. Applying structural equation modeling analysis to neuroimaging data has a particular advantage compared to applying it to economics, social sciences or psychology datasets, since the connections (or pathways) between the dependent variables (activity of brain areas) can be determined based on anatomical knowledge and the activity can also be measured directly. With applications in other fields, this is not always true: the models are sometimes hypothetical and cannot be measured directly.

Goodness-of-fit Criteria
Typically in SEM, statistical inference is used to measure: (1) the goodness of the overall fit of the model, i.e. how significantly different are the observed covariance structure and the covariance structure implied by the anatomical model, and (2) the difference between alternative models for modeling modulatory influence or experimental context by using the nested or stacked model approach. For the purpose of assessing the overall fit of the model, the 2 values relative to the degrees of freedom are most widely calculated. This is often referred to as the chi-square test and is an absolute test of model fit. If the p-value associated with the 2 value is below 0.05, the model is rejected in absolute fit sense. Because the 2 goodness-of-fit criterion is very sensitive to sample size and non-normality of the data, often other descriptive measures of fit are used in addition to the absolute 2 test. When the number of samples is greater than a few hundred, the 2 test has a high tendency to always show statistically significant results, ensuing in a rejected model. However other descriptive

fit statistics can be used in conjunction to the absolute test to assess the overall fit and are used to claim a model to be accepted though the 2 fit index may argue otherwise. Since the sample sizes in our analyses are too large for the 2 test, the 2 measure will not be used as the sole indicator of fit. A number of goodness-of-fit criteria have been formulated for SEM analyses; commonly used criteria include goodness-of-fit index (GFI), and adjusted GFI (AGFI). The GFI is essentially the ratio of the sum of the squared differences between the observed and implied covariance matrices to the observed variances. The AGFI is the adjusted version of GFI where the degrees of freedom of a model and the number of unknown variables are taken into consideration for adjustment. Both GFI and AGFI values fall between 0 and 1, where 0 represents no fit and 1 is a perfect fit (Hu and Bentler, 1999). Usually a value above 0.90 is considered acceptable, and a good fit. Other measures of fit used in this study are the root mean square residual (RMR) and the root mean square error approximation (RMSEA). RMR is the square root of the mean squared differences between sample variances and covariances, and estimated variances and covariances, so a smaller RMR value represents a better fit, and 0 represents a perfect fit. RMSEA incorporates the parsimony criterion and is relatively independent of sample size and number of parameters. A suggested rule of thumb for an RMSEA fit is that a value less than or equal to 0.06 indicates an adequate fit (Hu and Bentler, 1999).

Model Interpretation - Path Coefficients


The connection strength (path coefficient) represents the response of the dependent variable to a unit change in an explanatory variable when other variables in the model are held constant (Bollen, 1989). The path coefficients of a structural equation model are similar to correlation or regression coefficients and are interpreted as follows (McIntosh and GonzalezLima, 1994): A positive coefficient means that a unit increase in the activity measure of one structure leads to a direct increase in the activity measure of structures it projects to, proportional to the size of the coefficient. A negative coefficient means that an increase in the activity measure in one structure leads to a direct, proportional decrease in the activity measure of structures it projects to.

Differences in path coefficients for two different models (i.e., for two different conditions) can be of two types. A difference in the sign (without marked difference in absolute magnitude) reflects a reversal in the interactions within that pathway, or a qualitative change across conditions. In other words, the nature of the interaction between regions has changed. A difference in the absolute magnitude of the path coefficients (without sign change) is interpreted as a change in the strength of the influences conveyed through that pathway. The influence of a pathway or structure on the system is either increased or decreased according to the difference of the magnitude. A difference in the sign with marked difference in absolute magnitude suggests that there are discontinuities along these pathways, and these path coefficients are more difficult to interpret. (McIntosh and Gonzalez-Lima, 1992)

Nested Model Comparison


Since SEM is inherently linear, it cannot directly model non-linear changes in connection strength. However, to overcome this problem, two models can be constructed and these two models can be compared to test for non-linear changes. This is known as the nested (or stacked) model approach (McIntosh, 1998; Della-Maggiore et al., 2000). The first model defined in this approach is the restricted null model, in which the path coefficients are forced to be equal between all conditions and the second model is the corresponding alternate free model, in which the path coefficients are allowed to change between different conditions or subject groups. The 2 values are computed for both the null model and the alternative model with corresponding degrees of freedom. If the 2 value for the null model is statistically significantly larger than the alternative model, the null model is refuted and the alternative model is assumed to provide a better fit. In other words, different conditions within the free model are deemed to be significantly distinguishable in terms of their path connectivity, and one can infer that there is a statistically significant global difference in path coefficients between the conditions. The 2diff is evaluated with the degrees of freedom equal to the difference in the degrees of freedom for the null and free model. If the 2diff test for the null and free model is found to be statistically significant, one can also use pair-wise parameter comparisons (Arbuckle and Wothke, 1999) to determine which pairs of parameters are significantly different between the experimental conditions in the free model. For the pair-wise parameter comparison test, critical ratios for differences between two parameters in question are calculated by dividing the difference between the parameter estimates by an estimate of the standard error of the difference. Under appropriate assumptions and with a correct model, the critical ratios follow a standard normal distribution.

2. Effective Connectivity Analyses Using SEM


To further investigate the cortical interactions involved in auditory-visual speech perception, we performed structural equation modeling (SEM) analyses of our fMRI data. The SEM analyses were conducted on both normally hearing and deaf subjects to identify pathways that underlie the processing of visual speech. SEM is a multivariate technique used to analyze the covariance of observations (McIntosh et al., 1996). When applying SEM techniques, one also has to find a compromise between model complexity, anatomical accuracy and interpretability since there are mathematical constraints that impose limits to how complex the model can be.

Anatomical Models
Based on previous findings on functional specializations of brain regions known to be associated with visual and auditory stimulus processing, along with known anatomical connections in primates (see Discussion), a number of cortical regions were identified and used to construct a plausible, yet relatively simple anatomical model for our SEM analyses. Six cortical regions and their hypothesized connections comprised the structural model constructed for the effective connectivity analyses. Here the collections of connectivity data on the macaque brain (COCOMAC; http://www.cocomac.org) database was used extensively to search interconnectivity patterns reported in the literature. We hypothesized that there are projections from higher-order visual cortex (V2) to the fusiform gyrus (FG), the angular gyrus (AG), and to higher-order auditory cortex, more specifically the posterior superior temporal sulcus (STS). We further assumed projections from the FG and the AG to the STS. The opercular region of the inferior frontal gyrus (IFG, BA 44) and the lateral region of premotor cortex (PMC) brain areas that are generally believed to play a role in auditoryvisual speech perception and production were also included in our anatomical model and were assumed to have connectivity with AG, FG, and STS. To define an anatomical model that would best account for the underlying neural circuitry during auditory-visual speech perception in both the Hearing and Deaf groups, we searched through a set permissible functional connection patterns which included our conjectured connectivity mentioned above. After sorting through global fit measures for a set of connectivity patterns, we identified the following structural model (depicted as a path diagram in Figure 1) to provide the best fit across all subjects and two conditions.

IFG AG

V2

STS

PMC

FG

Figure 1 Anatomical model for SEM analyses (V2 = Secondary Visual Cortex, AG = Angular Gyrus, FG = Fusiform Gyrus, STS = Superior Temporal Sulcus, IFG = Inferior Frontal Gyrus, PMC = Premotor Cortex)

Data Extraction and Model Fitting


Activities in the cortical regions of interest (ROIs) of the SEM path models were extracted for all subjects for the CVCV Visual-Only and CVCV Audio-Visual conditions. For each subject, local maxima were identified within each region based on functional maps for the CVCV Visual-Only condition. The mni2tal algorithm (http://www.mrccbu.cam.ac.uk/Imaging) was used to transform the MNI coordinates into Talairach coordinates, and the Talairach Daemon client (http://ric.uthscsa.edu/TDinfo/) was used to identify the corresponding atlas labels and Brodmanns areas. BOLD signals in each ROI were extracted separately from the right and the left hemispheres using the Marsbar toolbox (http://marsbar.sourceforge.net) for experimental conditions. For each ROI of a single subject, the average signal was extracted using the SPM scaling design and the mean value option from a spherical region (r=5mm) centered at the peak activation coordinate. The extracted series from each temporal block were normalized for each subject and signal outliers were removed, and the first scan in each block (TR = 3s) was discarded to account for the delay in hemodynamic response. Finally, these values were concatenated across all subjects to create a single time-series for each ROI and experimental condition, and lastly the covariance matrix was calculated by treating these time-series as the measurements of the observed variables. The SEM analyses were conducted in AMOS 5 software (http://www.spss.com/amos/index.htm). Maximum likelihood estimation was performed on path coefficients between observed variables, thereby giving a measure of causal influence. The statistical significance of these parameter estimates was also computed.

Results
The structural model in Figure 1 was analyzed separately for the Hearing and the Deaf groups, and also separately for the left and the right hemispheres, resulting in four independent models Hearing (left hemisphere), Hearing (right hemisphere), Deaf (left hemisphere), and Deaf (right hemisphere). In order to investigate if any of the path models connection strengths change between the CVCV Visual-only and the CVCV Audio-Visual conditions (i.e. to test for changes in the connection strengths between when the auditory speech information is absent vs. available), multi-group analyses were conducted with the nested models approach. The null (constrained) models parameters were restricted to be equal between the two conditions, whereas the free (unconstrained) models parameters were allowed to be different for the two separate conditions. Several indices for goodness-of-fit, as discussed in the Methods section, for the four nested models are listed in Table 11 along with their 2 statistics for model comparisons. The goodness-of-fit indices indicate that the anatomical model (Figure 1) adequately fits the experimental data for both subject groups and for both hemispheres especially when the models were unconstrained. This implies that our anatomical model is suitably represents a network of cortical regions that may underlie a audio-visual speech processing for both subject groups, while being sensitive enough to the changes in the availability of auditory speech. The 2 fit index for the Hearing (Right) model suggested that the absolute fit may not be acceptable (2(6) = 12.771, P = 0.047) as its p-value is near the borderline cut-off point of P > 0.05, but as stated in the Methods section, other descriptive fit statistics (RMR = 0.013, GFI = 0.998, AFGI = 0.986, RMSEA = 0.024) reflect a good overall fit, hence this model was not rejected in our analyses. The stability index (Fox, 1980; Bentler and Freeman, 1983) was also calculated for each model since our path model includes a nonrecursive subset of regions: AG, FG, STS, IFG, and PMC. As listed in Table 11, both the Hearing and the Deaf right hemisphere models estimates were found to be well below one and thus stable. However, the Deaf (Left) models stability indices were all greater than one (STI = 2.387, 2.387, 1.131). If the stability index value is greater than or equal to one for any of the nonrecursive subsets of a path model, the parameter estimates are known to yield an unstable system, producing results that are particularly difficult to interpret. Therefore, we decided not to present the parameter estimates from the Deaf (Left) model. All nested models except for the Hearing (Left) model (2diff = 23.995, df = 15, P = 0.065) showed statistically significant differences across unconstrained and constrained models. Since the Hearing (Left) model did not satisfy the conventional level of significance p < 0.05, its path coefficients should be interpreted with some caution.

Goodness-of-fit Index Criteria Model


X2 P RMR GFI AGFI RMSEA

Stability Index
VO AV

df=15

2diff

Model Comparison
P

Hearing (Left) Unconstrained Constrained Hearing (Right) Unconstrained Constrained Deaf (Left) Unconstrained Constrained Deaf (Right) Unconstrained Constrained

3.237 27.232 12.771 40.810 8.638 36.981 5.982


40.641

.779 .163 .047 .006 .195 .017 .425


.006

.006 .024 .013 .023 .011 .020 .016


.020

.999 .996 .998 .993 .999 .994 .999


.994

.996 .991 .986 .987 .990 .988 .993


.987

.000 .012 .024 .022 .015 .019 .000


.021

.982 .977 .157 .183

.982 .157

23.995 28.039 28.343 34.658

.065 .003 .020 .021

2.387 2.387 1.141 .328 .328


1.042

Table 1 Goodness-of-fit indices for SEM

Tables 12 and 13 list the estimated path coefficients that minimize the difference between observed and model coefficients for the Hearing (Left and Right) and Deaf (Right) models along with their corresponding standard errors, critical ratios, and p-values for both the CVCV Visual-Only and CVCV Audio-Visual conditions. Here, the estimated path coefficients represent the strength of connections or the strength of the influence conveyed through that pathway. The last two columns of the table list critical ratios for pair-wise parameter differences between the two experimental tasks and their levels of significance. The estimated pathway connection strengths are also summarized graphically in Figures 10, 11 and 12 for the Hearing (Right), Hearing (Left) and the Deaf (Right) models respectively. In these figures, thicker arrows are used to represent pathways with statistically significant pair-wise differences in connection strengths across the two experimental tasks.

CVCV Visual-Only Model


Estimated path coefficient Standard Error Critical Ratio P-value Estimated path coefficient

CVCV Audio-Visual
Standard Error Critical Ratio P-value

Pairwise Comparison
Critical Ratio for Difference P-value

Hearing (Left)
V2 AG V2 FG V2 STS FG AG AG FG AG STS STS AG FG STS STS FG STS PMC PMC STS STS IFG IFG STS IFG PMC PMC IFG FG PMC AG PMC
.377 .493 .542 .136 .136 .761 .134 -.074 .133 .322 -.009 .969 -1.135 .161 .161 .070 .083 .353 .364 .263 .220 .220 .477 .054 .111 .145 .469 -.244 .513 -.182 .299 .299 .089 -.097 .035 .029 .126 .018 .018 .128 .057 .126 .053 .107 .212 .057 .225 .036 .036 .035 .066 .042 .047 .093 .034 .034 .110 .089 .181 .128 .107 .135 .047 .093 .017 .017 .053 .061 10.791 16.700 4.315 7.570 7.570 5.967 2.347 -.590 2.516 3.001 -.041 17.033 -5.045 4.436 4.436 2.022 1.259 8.412 7.715 2.841 6.462 6.462 4.331 .609 .611 1.133 4.397 -1.804 10.923 -1.956 17.620 17.620 1.668 -1.594 *** * *** *** *** *** *** *** *** *** *** * .555 * ** .967 *** *** *** *** * .208 *** *** ** *** *** *** .280 .581 .191 .175 .175 .644 .145 .321 -.041 .411 -.022 .942 -1.049 .178 .178 .053 -.040 .275 .410 .102 .274 .274 .271 .136 .194 -.008 .021 .451 .607 -.525 .288 .288 .173 .080 .031 .028 .110 .020 .020 .124 .061 .135 .056 .138 .284 .068 .216 .044 .044 .047 .069 .033 .029 .069 .023 .023 .113 .087 .113 .076 .111 .156 .052 .108 .023 .023 .050 .052 9.028 20.977 1.741 8.743 8.743 5.180 2.386 2.372 -.732 2.985 -.076 13.940 -4.868 4.064 4.064 1.123 -.585 8.465 13.963 1.462 11.845 11.845 2.397 1.554 1.726 -.105 .188 2.896 11.712 -4.867 12.586 12.586 3.436 1.555 ** *** *** *** *** *** *** *** * *** *** .082 *** *** *** * * .464 ** .939 *** *** *** *** .261 .558 *** *** -2.242 2.185 -2.549 1.448 1.448 -.800 .188 2.113 -2.260 .700 -.050 -.486 .604 .407 .407 -.302 -1.636 -1.744 .891 -1.718 1.444 1.444 -1.783 1.025 .434 -1.202 -2.335 2.697 1.621 -2.471 -.375 -.375 1.007 1.930 x * * ** * * * * **

Hearing(Right)
V2 AG V2 FG V2 STS FG AG AG FG AG STS STS AG FG STS STS FG STS PMC PMC STS STS IFG IFG STS IFG PMC PMC IFG FG PMC AG PMC

Table 2 Hearing group: estimated path coefficients [*** = p-value < 0.001; ** = p-value < 0.01; * = pvalue < 0.05]

IFG AG
.377 .280 .136 .175 .761 .644 .083 -.040 -1.134 -1.049 .969 .942 .161 .178

.134 .145

V2

.542 .191 .133 -.041 .493 .581 -.074 .321

STS
.322 .411

-.009 -.022

PMC

FG

.070 .053

Figure 2 Hearing (left): estimated path coefficients [black: CVCV Visual-Only, blue: CVCV AudioVisual]

IFG AG
.353 .275 .220 .274 .477 .271 -.097 .080 -.182 -.525 .513 .607 .299 .288

.054 .136

V2

.263 .102 .145 -.008 .364 .410 .111 .194

STS
.469 .021

-.244 .451

PMC

FG

.089 .173

Figure 3 Hearing (right): estimated path coefficients [black: CVCV Visual-Only, blue: CVCV AudioVisual]

CVCV Visual-Only Model


Estimated path coefficient Standard Error Critical Ratio Pvalue

CVCV Audio-Visual
Estimated path coefficient Standard Error Critical Ratio Pvalue

Pairwise Comparison
Critical Ratio for Difference Pvalue

Deaf (Right) V2 AG V2 FG V2 STS FG AG AG FG AG STS STS AG FG STS STS FG STS PMC PMC STS STS IFG IFG STS IFG PMC PMC IFG FG PMC AG PMC .392 .363 -.101 .377 .377 .594 -.249 .417 -.154 .375 -.093 .462 -.203 .302 .302 .026 -.023 .038 .032 .082 .052 .052 .120 .126 .103 .094 .144 .200 .042 .073 .021 .021 .058 .076 10.332 11.227 -1.223 7.239 7.239 4.951 -1.977 4.060 -1.629 2.607 -.467 11.089 -2.775 14.085 14.085 .439 -.298 *** ** *** *** ** *** *** *** * *** *** *** .294 .316 .090 .284 .284 .414 -.067 .164 .013 .208 .104 .579 -.328 .248 .248 .046 .168 .043 .036 .091 .039 .039 .182 .156 .154 .129 .206 .298 .069 .130 .031 .031 .048 .090 6.835 8.911 .987 7.289 7.289 2.274 -.430 1.064 .100 1.008 .350 8.374 -2.515 7.985 7.985 .960 1.881 *** * *** *** *** *** * *** *** -2.310 -1.103 2.425 -2.101 -2.101 -1.557 2.308 -1.847 1.585 -.863 .705 1.750 -.854 -1.742 -1.742 .316 2.124 * * * * * *

Table 3 Deaf group: estimated path coefficients [*** = p-value < 0.001; ** = p-value < 0.01; * = pvalue < 0.05]

IFG AG
.392 .294 .377 .284 .594 .414 -.023 .168 -.203 -.328 .462 .579 .302 .248

-.249 -.067

V2

-.101 .090 -.154 .013 .363 .316 .417 .164

STS
.375 .208

-.093 .104

PMC

FG

.026 .046

Figure 4 Deaf (right): estimated path coefficients [black: CVCV Visual-Only, blue: CVCV AudioVisual]

Tables 14 and 15 were also constructed to list direct, indirect, and combined total effects each node in the path diagram had on the other nodes. The estimated connection strengths listed in Tables 12 and 13 are equivalent to direct effects listed in Tables 14 and 15.
Visual-Only Audio-Visual

V2 Left FG IFG PMC AG STS Right


d i t d i t d i t d i t d i t
.493 .123 .615 .000 .430 .430 .000 .283 .283 .377 .137 .514 .542 -.145 .397

FG
.000 .020 .020 .000 .021 .021 .070 .018 .088 .136 .004 .140 -.074 .081 .007

IFG
.000 -.086 -.086 .000 -.560 -.560 .161 -.283 -.122 .000 -.086 -.086 -1.135 .577 -.558

PMC
.000 -.014 -.014 .161 -.094 .066 .000 -.022 -.022 .000 -.015 -.015 -.009 -.085 -.094

AG
.136 .058 .194 .000 .391 .391 .083 .198 .281 .000 .074 .074 .761 -.404 .357

STS
.133 -.059 .074 .969 -.466 .503 .322 -.076 .246 .134 -.060 .074 .000 -.522 -.522

V2
.581 .064 .645 .000 .340 .340 .000 .209 .209 .280 .160 .440 .191 .130 .321

FG
.000 .028 .028 .000 .235 .235 .053 .124 .177 .175 .036 .212 .321 -.105 .216

IFG
.000 .008 .008 .000 -.530 -.530 .178 -.312 -.133 .000 -.077 -.077 -1.049 .512 -.537 .000 -.011 -.011 .000 -.151 -.151 .288 -.057 .231 .000 -.052 -.052 -.525 -.044 .167

PMC
.000 .002 .002 .178 -.106 .073 .000 -.030 -.030 .000 -.015 -.015 -.022 -.085 -.106 .000 .009 .009 .288 .209 .497 .000 .153 .153 .000 .039 .039 .451 -.021 -.179

AG
.175 .000 .175 .000 .372 .372 -.040 .220 .180 .000 .083 .083 .644 -.284 .361 .274 .033 .307 .000 .265 .265 .080 .147 .227 .000 .129 .129 .271 -.030 .058

STS
-.041 .033 -.008 .942 -.424 .517 .411 -.119 .292 .145 -.075 .070 .000 -.506 -.506 -.008 .034 .026 .607 -.047 .560 .021 .172 .193 .136 -.016 .120 .000 -.192 -.169

.364 .000 .000 .000 .220 .145 .410 .000 d .171 .078 -.037 -.044 .085 -.012 .124 .091 i .536 .078 -.037 -.044 .305 .133 .535 .091 t .000 .000 .000 .299 .000 .513 .000 .000 d .309 .142 -.065 -.161 .295 .068 .239 .267 i IFG .309 .142 -.065 .138 .295 .581 .239 .267 t .000 .089 .299 .000 -.097 .469 .000 .173 d .294 .102 -.127 -.084 .316 .088 .205 .126 PMC i .294 .191 .172 -.084 .220 .557 .205 .299 t .353 .220 .000 .000 .000 .054 .275 .274 d .141 .026 -.020 -.024 .091 .019 .187 .065 i AG .494 .246 -.020 -.024 .091 .073 .462 .340 t .263 .111 -.182 -.244 .477 .000 .102 .194 d .167 .054 -.044 -.021 -.030 -.192 .167 .054 i STS .430 .164 -.226 -.265 .447 -.192 .196 .104 t Table 4 Hearing group: estimated parameters for direct, indirect and total effects

FG

Visual-Only

Audio-Visual

V2 Right FG

FG

IFG

PMC

AG

STS

V2

FG

IFG
.000 .002 .002 .000 -.112 -.112 .248 -.080 .168 .000 .018 .018 -.328 .062 -.266

PMC
.000 .000 .000 .248 .030 .278 .000 .073 .073 .000 -.001 -.001 .104 -.084 .020

AG
.284 .022 .306 .000 .332 .332 .168 .193 .362 .000 .059 .059 .414 .004 .417

STS
.013 -.018 -.006 .579 -.027 .552 .208 .091 .299 -.067 .010 -.057 .000 -.174 -.174

.363 .000 .000 .000 .377 -.154 .316 .000 d .134 .024 .048 .032 -.105 -.037 .117 .086 i .498 .024 .048 .032 .272 -.190 .433 .086 t .000 .000 .000 .302 .000 .462 .000 .000 d .215 .317 -.006 -.041 .362 -.044 .210 .198 i IFG .215 .317 -.006 .261 .362 .418 .210 .198 t .193 .275 -.065 .037 .335 .000 .000 .046 d .000 .026 .302 .000 -.023 .375 .197 .155 PMC i .193 .300 .237 .037 .312 .375 .197 .201 t .103 -.113 .060 .040 -.042 .013 .294 .284 d .392 .377 .000 .000 .000 -.249 .105 .007 i AG .495 .263 .060 .040 -.042 -.236 .398 .292 t .440 .074 .035 -.019 -.014 -.339 .090 .164 d -.101 .417 -.203 -.093 .594 .000 .187 .091 i STS .339 .491 -.168 -.112 .580 -.339 .278 .255 t Table 5 Deaf group: estimated parameters for direct, indirect and total effects

Arbuckle J, Wothke W (1999) AMOS 4.0 user's guide. In. Chicago: Smallwaters Corportaion, Inc. Bentler PM, Freeman EH (1983) Tests for stability in linear structural equation systems. Psychometrika 48:143-145. Della-Maggiore V, Sekuler AB, Grady CL, Bennett PJ, Sekuler R, McIntosh AR (2000) Corticolimbic interactions associated with performance on a short-term memory task are modified by age. J Neurosci 20:8410-8416. Fox J (1980) Effect analysis in structural equation models. Sociological Methods and Research 9:3-28. Hu L, Bentler P (1999) Cutoff criteria for fit indices in covariance structure analysis: conventional criteria versus new alternatives. Structural Equation Modeling 6:1-55. McIntosh A, R., Gonzalez-Lima F (1992) The application of structural modeling to metabolic mapping of functional neural systems. In: NATO AS1 series: Advances in metabolic mapping techniques for brain imaging of behavioral and learning functions (Gonzalez-Lima F, Finkenstadt T, Scheich H, eds), pp 219-258. Dordrecht: Kluwer Academic. McIntosh A, R., Gonzalez-Lima F (1994) Structural equation modeling and its application to network analysis in functional brain imaging. Hum Brain Mapp 2. McIntosh AR (1998) Understanding neural interactions in learning and memory using functional neuroimaging. Ann N Y Acad Sci 855:556-571. McIntosh AR, Grady CL, Haxby JV, Ungerleider LG, Horwitz B (1996) Changes in limbic and prefrontal functional interactions in a working memory task for faces. Cereb Cortex 6:571-584.

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