Aaron N. McInnes , Sarah T. Olsen , Christi R.P. Sullivan, Dawson C. Cooper, Saydra Wilson, Ayse Irem Sonmez, C. Sophia Albott, Stephen C. Olson, Carol B. Peterson, Barry R. Rittberg, Alexander Herman, Matej Bajzer, Ziad Nahas, Alik S. Widge
{"title":"经颅磁刺激治疗抑郁症的轨迹建模和反应预测","authors":"Aaron N. McInnes , Sarah T. Olsen , Christi R.P. Sullivan, Dawson C. Cooper, Saydra Wilson, Ayse Irem Sonmez, C. Sophia Albott, Stephen C. Olson, Carol B. Peterson, Barry R. Rittberg, Alexander Herman, Matej Bajzer, Ziad Nahas, Alik S. Widge","doi":"10.1016/j.pmip.2024.100135","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>Repetitive transcranial magnetic stimulation (rTMS) therapy could be improved by more accurate and earlier prediction of response. Latent class mixture (LCMM) and non-linear mixed effects (NLME) modeling have been applied to model the trajectories of antidepressant response (or non-response) to TMS, but it is not known whether such models are useful in predicting clinically meaningful change in symptom severity, i.e. categorical (non)response as opposed to continuous scores.</p></div><div><h3>Methods</h3><p>We compared LCMM and NLME approaches to model the antidepressant response to TMS in a naturalistic sample of 238 patients receiving rTMS for treatment resistant depression, across multiple coils and protocols. We then compared the predictive power of those models.</p></div><div><h3>Results</h3><p>LCMM trajectories were influenced largely by baseline symptom severity, but baseline symptoms provided little predictive power for later antidepressant response. Rather, the optimal LCMM model was a nonlinear two-class model that accounted for baseline symptoms. This model accurately predicted patient response at 4 weeks of treatment (AUC=0.70, 95 % CI=[0.52–0.87]), but not before. NLME offered slightly improved predictive performance at 4 weeks of treatment (AUC=0.76, 95 % CI=[0.58–0.94], but likewise, not before.</p></div><div><h3>Conclusions</h3><p>In showing the predictive validity of these approaches to model response trajectories to rTMS, we provided preliminary evidence that trajectory modeling could be used to guide future treatment decisions.</p></div>","PeriodicalId":19837,"journal":{"name":"Personalized Medicine in Psychiatry","volume":"47 ","pages":"Article 100135"},"PeriodicalIF":0.0000,"publicationDate":"2024-08-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Trajectory modeling and response prediction in transcranial magnetic stimulation for depression\",\"authors\":\"Aaron N. McInnes , Sarah T. Olsen , Christi R.P. Sullivan, Dawson C. Cooper, Saydra Wilson, Ayse Irem Sonmez, C. Sophia Albott, Stephen C. Olson, Carol B. Peterson, Barry R. Rittberg, Alexander Herman, Matej Bajzer, Ziad Nahas, Alik S. Widge\",\"doi\":\"10.1016/j.pmip.2024.100135\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>Repetitive transcranial magnetic stimulation (rTMS) therapy could be improved by more accurate and earlier prediction of response. Latent class mixture (LCMM) and non-linear mixed effects (NLME) modeling have been applied to model the trajectories of antidepressant response (or non-response) to TMS, but it is not known whether such models are useful in predicting clinically meaningful change in symptom severity, i.e. categorical (non)response as opposed to continuous scores.</p></div><div><h3>Methods</h3><p>We compared LCMM and NLME approaches to model the antidepressant response to TMS in a naturalistic sample of 238 patients receiving rTMS for treatment resistant depression, across multiple coils and protocols. We then compared the predictive power of those models.</p></div><div><h3>Results</h3><p>LCMM trajectories were influenced largely by baseline symptom severity, but baseline symptoms provided little predictive power for later antidepressant response. Rather, the optimal LCMM model was a nonlinear two-class model that accounted for baseline symptoms. This model accurately predicted patient response at 4 weeks of treatment (AUC=0.70, 95 % CI=[0.52–0.87]), but not before. NLME offered slightly improved predictive performance at 4 weeks of treatment (AUC=0.76, 95 % CI=[0.58–0.94], but likewise, not before.</p></div><div><h3>Conclusions</h3><p>In showing the predictive validity of these approaches to model response trajectories to rTMS, we provided preliminary evidence that trajectory modeling could be used to guide future treatment decisions.</p></div>\",\"PeriodicalId\":19837,\"journal\":{\"name\":\"Personalized Medicine in Psychiatry\",\"volume\":\"47 \",\"pages\":\"Article 100135\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-08-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Personalized Medicine in Psychiatry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2468171724000218\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Personalized Medicine in Psychiatry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2468171724000218","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Trajectory modeling and response prediction in transcranial magnetic stimulation for depression
Background
Repetitive transcranial magnetic stimulation (rTMS) therapy could be improved by more accurate and earlier prediction of response. Latent class mixture (LCMM) and non-linear mixed effects (NLME) modeling have been applied to model the trajectories of antidepressant response (or non-response) to TMS, but it is not known whether such models are useful in predicting clinically meaningful change in symptom severity, i.e. categorical (non)response as opposed to continuous scores.
Methods
We compared LCMM and NLME approaches to model the antidepressant response to TMS in a naturalistic sample of 238 patients receiving rTMS for treatment resistant depression, across multiple coils and protocols. We then compared the predictive power of those models.
Results
LCMM trajectories were influenced largely by baseline symptom severity, but baseline symptoms provided little predictive power for later antidepressant response. Rather, the optimal LCMM model was a nonlinear two-class model that accounted for baseline symptoms. This model accurately predicted patient response at 4 weeks of treatment (AUC=0.70, 95 % CI=[0.52–0.87]), but not before. NLME offered slightly improved predictive performance at 4 weeks of treatment (AUC=0.76, 95 % CI=[0.58–0.94], but likewise, not before.
Conclusions
In showing the predictive validity of these approaches to model response trajectories to rTMS, we provided preliminary evidence that trajectory modeling could be used to guide future treatment decisions.