Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where Petra Ludäscher is active.

Publication


Featured researches published by Petra Ludäscher.


Journal of Nervous and Mental Disease | 2008

Motives for nonsuicidal self-injury among women with borderline personality disorder.

Nikolaus Kleindienst; Martin Bohus; Petra Ludäscher; Matthias F. Limberger; Katrin Kuenkele; Ulrich Ebner-Priemer; Alexander L. Chapman; Markus Reicherzer; Rolf-Dieter Stieglitz; Christian Schmahl

Patients with borderline personality disorder (BPD) are known to use nonsuicidal self-injury (NSSI) as a dysfunctional strategy to regulate intense emotions. The primary purpose of this study was to clarify the motives for NSSI along with their interrelations. We further investigated the variety of emotions preceding NSSI and possible effects of NSSI on these emotions. To this end, a structured self-rating questionnaire on NSSI was administered to 101 female BPD-patients exhibiting NSSI. Most patients reported multiple motives for NSSI. The motives were more likely to compound than to exclude one another. Negative reinforcement was almost always involved in NSSI, whereas positive reinforcement (e.g., “getting a kick”) played an additional role among about half of the patients. NSSI was usually preceded by a large variety of negative feelings that were reported to clearly improve with NSSI. In conclusion, therapists should anticipate a multidimensional functional spectrum when exploring motives of NSSI.


Psychiatry Research-neuroimaging | 2007

Elevated pain thresholds correlate with dissociation and aversive arousal in patients with borderline personality disorder

Petra Ludäscher; Martin Bohus; Klaus Lieb; Alexandra Philipsen; Anja Jochims; Christian Schmahl

In addition to reduced pain perception, patients with borderline personality disorder (BPD) show higher pain thresholds under subjective stress conditions as compared with non-stress conditions. However, the correlation between symptoms of stress and pain thresholds has not been investigated so far. Using a new and convenient methodology, electric stimulation, we expected higher pain and detection thresholds in patients with BPD than in to healthy controls as well as a positive correlation between pain thresholds and symptoms of stress (aversive arousal and dissociation) in BPD patients. Twelve female patients with BPD and twelve healthy controls were included in the study. Electric stimulation was applied on the right index finger, and detection and pain thresholds were assessed by gradually intensifying the stimuli. We found significantly elevated pain thresholds in patients with BPD as compared with healthy controls, but no difference between patients and controls in detection thresholds. In patients, a significant positive correlation was revealed between pain thresholds and dissociation as well as between pain thresholds and aversive arousal. Besides demonstrating a close correlation between pain thresholds and symptoms of stress in patients with BPD, this study replicated earlier findings of reduced pain perception in patients with BPD. Measuring electric pain thresholds is a valid and reasonable method for larger studies.


Acta Psychiatrica Scandinavica | 2009

A cross-sectional investigation of discontinuation of self-injury and normalizing pain perception in patients with borderline personality disorder

Petra Ludäscher; Wolfgang Greffrath; Christian Schmahl; Nikolaus Kleindienst; Anja Kraus; Ulf Baumgärtner; Walter Magerl; R.-D. Treede; Martin Bohus

Objective:  Several studies have shown reduced pain perception in patients with borderline personality disorder (BPD) and current self‐injurious behavior (SIB). The aim of the present study was to test whether pain perception in patients with current SIB is different from that of patients who had stopped SIB, and whether pain perception of the latter group differs from healthy controls (HC).


World Journal of Biological Psychiatry | 2008

Pain sensitivity is reduced in borderline personality disorder, but not in posttraumatic stress disorder and bulimia nervosa.

Christian Schmahl; Miriam Meinzer; Andrea Zeuch; Manfred M. Fichter; Marian Cebulla; Nikolaus Kleindienst; Petra Ludäscher; Regina Steil; Martin Bohus

Background. Several studies revealed reduced pain sensitivity in patients suffering from borderline personality disorder (BPD) under baseline and stress conditions. To establish whether these findings are specific for BPD, we compared pain thresholds in patients with BPD, posttraumatic stress disorder (PTSD), bulimia nervosa, and healthy controls. Methods. The study included 76 female subjects: 16 patients with BPD, 16 patients with PTSD, 20 patients with bulimia nervosa and 24 healthy controls. Heat and cold pain thresholds were assessed under baseline and stress conditions, using a contact thermode. Mental stress was induced by the Paced Auditory Serial Addition Task. Results. Under baseline conditions, pain thresholds in patients with BPD were significantly higher compared to healthy controls. Patients with PTSD and bulimia nervosa did not show significant differences in pain thresholds compared to healthy controls. Under stress conditions, the difference between BPD patients and healthy controls became even more prominent, whereas the results in the other patient groups remained insignificant. Conclusions. Our results support the hypothesis that reduced pain sensitivity is a prominent feature of BPD, which may differentiate this disorder from other stress-related psychiatric conditions.


PLOS ONE | 2012

COMT val158met Polymorphism and Neural Pain Processing

Christian Schmahl; Petra Ludäscher; Wolfgang Greffrath; Anja Kraus; Gabriele Valerius; Thomas G. Schulze; Marcella Rietschel; Michael N. Smolka; Martin Bohus

A functional polymorphism (val158met) of the gene coding for Catechol-O-methyltransferase (COM) has been demonstrated to be related to processing of emotional stimuli. Also, this polymorphism has been found to be associated with pain regulation in healthy subjects. Therefore, we investigated a possible influence of this polymorphism on pain processing in healthy persons as well as in subjects with markedly reduced pain sensitivity in the context of Borderline Personality Disorder (BPD). Fifty females (25 patients with BPD and 25 healthy control participants) were included in this study. Genotype had a significant – though moderate - effect on pain sensitivity, but only in healthies. The number of val alleles was correlated with the BOLD response in several pain-processing brain regions, including dorsolateral prefrontal cortex, posterior parietal cortex, lateral globus pallidus, anterior and posterior insula. Within the subgroup of healthy participants, the number of val alleles was positively correlated with the BOLD response in posterior parietal, posterior cingulate, and dorsolateral prefrontal cortex. BPD patients revealed a positive correlation between the number of val alleles and BOLD signal in anterior and posterior insula. Thus, our data show that the val158met polymorphism in the COMT gene contributes significantly to inter-individual differences in neural pain processing: in healthy people, this polymorphism was more related to cognitive aspects of pain processing, whereas BPD patients with reduced pain sensitivity showed an association with activity in brain regions related to affective pain processing.


International Clinical Psychopharmacology | 2012

Evaluation of naltrexone for dissociative symptoms in borderline personality disorder

Christian Schmahl; Nikolaus Kleindienst; Matthias F. Limberger; Petra Ludäscher; Jana Mauchnik; Peter Deibler; Sonja Brünen; Christoph Hiemke; Klaus Lieb; Sabine C. Herpertz; Markus Reicherzer; Mathias Berger; Martin Bohus

Data from a pilot study suggest that naltrexone might reduce dissociative symptoms in patients with borderline personality disorder. However, the interpretation of these data is limited by the lack of a control group and by the nonblind nature of this study. Hence, we examined the effects of naltrexone using a more rigorous design that controlled for major confounders such as spontaneous reduction of dissociation over time and placebo effects. Unmedicated patients with BPD [according to Diagnostic and Statistical Manual of Mental Disorders-IVth edition (DSM-IV)] were included in two small double-blind placebo-controlled randomized trials (total n=29). Patients received both 3 weeks of naltrexone (50 or 200 mg/day) and 3 weeks of placebo in a randomized order. Twenty-five patients completed the study according to protocol. Dissociation under naltrexone and placebo, respectively, was compared by repeated-measures analyses of variance. In either trial, both the intensity and duration of dissociative symptoms were numerically lower under naltrexone than under placebo. However, the effects were too small to reach statistical significance. Our data provide the first estimate of the pure pharmacological antidissociative efficacy of naltrexone from a rigorously designed trial.


Journal of Psychopharmacology | 2015

No evidence for differential dose effects of hydrocortisone on intrusive memories in female patients with complex post-traumatic stress disorder – a randomized, double-blind, placebo-controlled, crossover study

Petra Ludäscher; Christian Schmahl; Robert E. Feldmann; Nikolaus Kleindienst; Miriam Schneider; Martin Bohus

Background: Post-traumatic stress disorder is characterized by intrusive traumatic memories. Presently, a controversial debate is ongoing regarding whether reduced cortisol secretion in post-traumatic stress disorder promotes an automatic retrieval of trauma-associated memories. Hence, a pharmacological elevation of cortisol was proposed to decrease post-traumatic stress disorder symptoms, particularly intrusions. The present study investigated the impact of two different doses of hydrocortisone on automatic memory retrieval using a randomized, double-blind, placebo-controlled, crossover study in 30 inpatients with post-traumatic stress disorder. Methods: All participants were female and received various psychotropic medications. They were randomly assigned to one of two groups within a crossover design: they received either 1 week placebo followed by 1 week hydrocortisone 10/d, followed by 1 week placebo, followed by hydrocortisone 30 mg/d (15 participants) or 1 week hydrocortisone 30 mg/d, followed by 1 week placebo, followed by 1 week hydrocortisone 10 mg/d, followed by 1 week placebo (15 participants). The outcome measures were the frequency and the intensity of intrusions, the overall symptomatology of post-traumatic stress disorder and the general psychopathology. Results: We did not find any differences in the frequency and the intensity of post-traumatic stress disorder-related intrusions between the 10 mg hydrocortisone, the 30 mg hydrocortisone and the placebo condition. All effect sizes for the hydrocortisone condition vs. placebo were very small. Additionally, the overall symptomatology of post-traumatic stress disorder and the general psychopathology did not differ between the hydrocortisone therapies and placebo. Conclusions: Our results do not show any effect of the hydrocortisone administration on intrusions in complex post-traumatic stress disorder.


Schmerz | 2006

Schmerzverarbeitung bei Borderline-Persönlichkeitsstörung, Fibromyalgie und Posttraumatischer Belastungsstörung

Anja Jochims; Petra Ludäscher; Martin Bohus; Rolf-Detlef Treede; Christian Schmahl

ZusammenfassungDiese Übersicht fasst relevante experimentelle Studien zur Schmerzwahrnehmung und Schmerzverarbeitung bei ausgewählten psychiatrischen Störungsbildern zusammen, bei denen traumatischer Stress in der Ätiologie eine Rolle spielt. Bei der Borderline-Persönlichkeitsstörung, der Posttraumatischen Belastungsstörung und der Fibromyalgie bestehen Hinweise auf unterschiedliche neurophysiologische und neuropsychologische Schmerzverarbeitungsmuster. Experimentelle Studien bei Borderline-Patienten zeigen eine Desensibilisierung hinsichtlich der Schmerzschwellen, Fibromyalgiepatienten weisen ein entgegengesetztes Muster auf, welches auf eine zentrale Sensibilisierung hinweist. Es wird weiterhin ein kurzer Überblick über Methoden zur Erhebung der Schmerzwahrnehmung (peripher und zentral) sowie zu neurobiologischen Mechanismen der Schmerzverarbeitung gegeben. Hier wird im Besonderen auf die Unterscheidung zwischen dem sensorisch-diskriminativen System und dem affektiv-motivationalen System Bezug genommen. Bezogen auf den Ergebnisstand der aktuellen Forschung werden ein Ausblick auf zukünftige Forschung und therapeutische Implikationen dargestellt.AbstractThe authors review relevant experimental studies on pain perception and processing in psychiatric disorders with traumatic stress as an etiological factor. In borderline personality disorder, post-traumatic stress disorder, and fibromyalgia neurophysiological and neuropsychological patterns of pain processing appear to be different. Experimental studies in borderline patients show a desensitization of pain thresholds whereas patients with fibromyalgia show an opposite pattern, which could be explained by a central augmentation of pain processing. Furthermore, the authors outline methods to assess pain perception (peripheral and central) and describe the neurobiological mechanisms of pain processing, particularly the distinction between the sensory-discriminative lateral system and the affective-motivational medial system. Finally, suggestions for further research and implications for therapy are proposed.The authors review relevant experimental studies on pain perception and processing in psychiatric disorders with traumatic stress as an etiological factor. In borderline personality disorder, post-traumatic stress disorder, and fibromyalgia neurophysiological and neuropsychological patterns of pain processing appear to be different. Experimental studies in borderline patients show a desensitization of pain thresholds whereas patients with fibromyalgia show an opposite pattern, which could be explained by a central augmentation of pain processing. Furthermore, the authors outline methods to assess pain perception (peripheral and central) and describe the neurobiological mechanisms of pain processing, particularly the distinction between the sensory-discriminative lateral system and the affective-motivational medial system. Finally, suggestions for further research and implications for therapy are proposed.


Schmerz | 2006

[Pain processing in patients with borderline personality disorder, fibromyalgia, and post-traumatic stress disorder].

Anja Jochims; Petra Ludäscher; Martin Bohus; Rolf-Detlef Treede; Christian Schmahl

ZusammenfassungDiese Übersicht fasst relevante experimentelle Studien zur Schmerzwahrnehmung und Schmerzverarbeitung bei ausgewählten psychiatrischen Störungsbildern zusammen, bei denen traumatischer Stress in der Ätiologie eine Rolle spielt. Bei der Borderline-Persönlichkeitsstörung, der Posttraumatischen Belastungsstörung und der Fibromyalgie bestehen Hinweise auf unterschiedliche neurophysiologische und neuropsychologische Schmerzverarbeitungsmuster. Experimentelle Studien bei Borderline-Patienten zeigen eine Desensibilisierung hinsichtlich der Schmerzschwellen, Fibromyalgiepatienten weisen ein entgegengesetztes Muster auf, welches auf eine zentrale Sensibilisierung hinweist. Es wird weiterhin ein kurzer Überblick über Methoden zur Erhebung der Schmerzwahrnehmung (peripher und zentral) sowie zu neurobiologischen Mechanismen der Schmerzverarbeitung gegeben. Hier wird im Besonderen auf die Unterscheidung zwischen dem sensorisch-diskriminativen System und dem affektiv-motivationalen System Bezug genommen. Bezogen auf den Ergebnisstand der aktuellen Forschung werden ein Ausblick auf zukünftige Forschung und therapeutische Implikationen dargestellt.AbstractThe authors review relevant experimental studies on pain perception and processing in psychiatric disorders with traumatic stress as an etiological factor. In borderline personality disorder, post-traumatic stress disorder, and fibromyalgia neurophysiological and neuropsychological patterns of pain processing appear to be different. Experimental studies in borderline patients show a desensitization of pain thresholds whereas patients with fibromyalgia show an opposite pattern, which could be explained by a central augmentation of pain processing. Furthermore, the authors outline methods to assess pain perception (peripheral and central) and describe the neurobiological mechanisms of pain processing, particularly the distinction between the sensory-discriminative lateral system and the affective-motivational medial system. Finally, suggestions for further research and implications for therapy are proposed.The authors review relevant experimental studies on pain perception and processing in psychiatric disorders with traumatic stress as an etiological factor. In borderline personality disorder, post-traumatic stress disorder, and fibromyalgia neurophysiological and neuropsychological patterns of pain processing appear to be different. Experimental studies in borderline patients show a desensitization of pain thresholds whereas patients with fibromyalgia show an opposite pattern, which could be explained by a central augmentation of pain processing. Furthermore, the authors outline methods to assess pain perception (peripheral and central) and describe the neurobiological mechanisms of pain processing, particularly the distinction between the sensory-discriminative lateral system and the affective-motivational medial system. Finally, suggestions for further research and implications for therapy are proposed.


Borderline Personality Disorder and Emotion Dysregulation | 2016

Women with exposure to childhood interpersonal violence without psychiatric diagnoses show no signs of impairment in general functioning, quality of life and sexuality

Sophie Rausch; Julia Herzog; Janine Thome; Petra Ludäscher; Meike Müller-Engelmann; Regina Steil; Kathlen Priebe; Thomas Fydrich; Nikolaus Kleindienst

BackgroundChildhood interpersonal violence is a major risk factor for developing Posttraumatic Stress Disorder (PTSD), other axis-I disorders or Borderline Personality Disorder (BPD). Individuals with a history of childhood sexual abuse (CSA) and childhood physical abuse (CPA) who meet the criteria of any axis-I disorder usually also exhibit general psychopathologic symptoms and impairments in quality of life and sexuality. The present study investigates whether women with a history of potentially traumatic CSA/CPA without any axis-I disorder or BPD show subthreshold symptoms of PTSD-specific and general psychopathology and impairments in global functioning, quality of life, and sexuality.MethodsData were obtained from N = 92 female participants: n = 31 participants with a history of potentially traumatic CSA/CPA (defined as fulfilling PTSD criterion A) without any axis-I disorder or BPD; n = 31 participants with PTSD related to CSA/CPA; and n = 30 healthy controls without any traumatic experiences. All three groups were matched for age and education. Those with a history of CSA/CPA with and without PTSD were further matched with regard to severity of physical and sexual abuse.ResultsWhile women with a history of potentially traumatic CSA/CPA without axis-I disorder or BPD clearly differed from the PTSD-group in the collected measures, they did not differ from healthy controls (e.g., GAF:87, BSI:0.3, BDI-II:4.5). They showed neither PTSD-specific nor general subthreshold symptoms nor any measurable restrictions in quality of life or sexual satisfaction.ConclusionsWomen with a history of potentially traumatic childhood interpersonal violence without axis-I disorder or BPD show a high level of functioning and a low level of pathological impairment that are comparable to the level of healthy controls. Further studies are needed to identify what helped these women survive these potentially traumatic experiences without developing any mental disorders.Trial registrationGerman Clinical Trials Registration ID: DRKS00006095. Registered 21 May 2014.

Collaboration


Dive into the Petra Ludäscher's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Regina Steil

Goethe University Frankfurt

View shared research outputs
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar
Top Co-Authors

Avatar

Thomas Fydrich

Humboldt University of Berlin

View shared research outputs
Top Co-Authors

Avatar
Researchain Logo
Decentralizing Knowledge