Rasch analysis of the PANSS negative subscale and exploration of negative symptom trajectories in first-episode schizophrenia – data from the OPTiMiSE trial
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Rasch analysis of the PANSS negative subscale and exploration of negative symptom trajectories in first-episode schizophrenia – data from the OPTiMiSE trial. / Baandrup, Lone; Allerup, Peter; Nielsen, Mette; Bak, Nikolaj; Düring, Signe W.; Leucht, Stefan; Galderisi, Silvana; Mucci, Armida; Bucci, Paola; Arango, Celso; Díaz-Caneja, Covadonga M.; Dazzan, Paola; McGuire, Philip; Demjaha, Arsime; Ebdrup, Bjørn H.; Kahn, René S.; Glenthøj, Birte Y.
In: Psychiatry Research, Vol. 289, 112970, 07.2020.Research output: Contribution to journal › Journal article › Research › peer-review
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T1 - Rasch analysis of the PANSS negative subscale and exploration of negative symptom trajectories in first-episode schizophrenia – data from the OPTiMiSE trial
AU - Baandrup, Lone
AU - Allerup, Peter
AU - Nielsen, Mette
AU - Bak, Nikolaj
AU - Düring, Signe W.
AU - Leucht, Stefan
AU - Galderisi, Silvana
AU - Mucci, Armida
AU - Bucci, Paola
AU - Arango, Celso
AU - Díaz-Caneja, Covadonga M.
AU - Dazzan, Paola
AU - McGuire, Philip
AU - Demjaha, Arsime
AU - Ebdrup, Bjørn H.
AU - Kahn, René S.
AU - Glenthøj, Birte Y.
PY - 2020/7
Y1 - 2020/7
N2 - The observed heterogeneity in negative symptom treatment response may be partly attributable to inadequate measurement tools or limitations in methods of analysis. Previous Item Response Theory models of the Positive and Negative Syndrome Scale (PANSS) have only examined samples of chronic patients and with mixed results. We examined the scalability of the negative subscale embedded in the PANSS and subsequently explored negative symptom trajectories across four weeks of amisulpride treatment. Data were derived from the OPTiMiSE trial comprising 446 patients with first-episode schizophrenia or schizophreniform disorder. Using the Rasch Model to examine psychometric properties of the PANSS negative subscale, we found that the composite score across items was not an adequate measure of negative symptom severity. Consequently, we chose an exploratory statistical approach involving Principal Component Analysis which yielded one significant component clustering into two significant symptom trajectories: 1) Subtle but constant decrease in negative symptom severity (N = 323; 72%), and 2) symptom instability across visits (N = 19; 4%). Explorative analytic methods as presented here may pave the way for more efficient and sensitive methods of analyzing negative symptom response in research and in clinical practice.
AB - The observed heterogeneity in negative symptom treatment response may be partly attributable to inadequate measurement tools or limitations in methods of analysis. Previous Item Response Theory models of the Positive and Negative Syndrome Scale (PANSS) have only examined samples of chronic patients and with mixed results. We examined the scalability of the negative subscale embedded in the PANSS and subsequently explored negative symptom trajectories across four weeks of amisulpride treatment. Data were derived from the OPTiMiSE trial comprising 446 patients with first-episode schizophrenia or schizophreniform disorder. Using the Rasch Model to examine psychometric properties of the PANSS negative subscale, we found that the composite score across items was not an adequate measure of negative symptom severity. Consequently, we chose an exploratory statistical approach involving Principal Component Analysis which yielded one significant component clustering into two significant symptom trajectories: 1) Subtle but constant decrease in negative symptom severity (N = 323; 72%), and 2) symptom instability across visits (N = 19; 4%). Explorative analytic methods as presented here may pave the way for more efficient and sensitive methods of analyzing negative symptom response in research and in clinical practice.
KW - Composite score
KW - Item response theory
KW - Rating scale
KW - Symptom relief
KW - Treatment response
U2 - 10.1016/j.psychres.2020.112970
DO - 10.1016/j.psychres.2020.112970
M3 - Journal article
C2 - 32438207
AN - SCOPUS:85084521245
VL - 289
JO - Psychiatry Research
JF - Psychiatry Research
SN - 0165-1781
M1 - 112970
ER -
ID: 242407497