Skip to main content
Erschienen in:

01.06.2019 | PTSD (S Creech and L Sippel, Section Editors)

Augmenting Treatment for Posttraumatic Stress Disorder and Co-Occurring Conditions with Oxytocin

verfasst von: Julianne C. Flanagan, PhD, Jennifer M. Mitchell, PhD

Erschienen in: Current Treatment Options in Psychiatry | Ausgabe 2/2019

Einloggen, um Zugang zu erhalten

Abstract

Purpose of Review

The goal of this manuscript is to review the extant literature examining the neurobiological and behavioral mechanisms underlying the potential utility of intranasal oxytocin as a novel pharmacologic intervention for the treatment of posttraumatic stress disorder (PTSD) and for the treatment of comorbid PTSD and alcohol and substance use disorders.

Recent Findings

Research indicates that intranasal oxytocin is a low-cost and easily accessible medication with an excellent safety profile. Oxytocin holds promise for facilitating more effective PTSD treatment, particularly when used in combination with evidence-supported psychotherapy interventions. There is still a significant need to identify the mechanisms of action underlying oxytocin treatment of PTSD and to maximize methods of nasal spray delivery, examine dose-response outcomes, and clarify the characteristics of individuals and populations that are most likely to benefit from adjunctive oxytocin treatment.

Summary

Collectively, preclinical and human laboratory research suggest that oxytocin may be an effective mechanism by which treatment outcomes for PTSD and common comorbidities can be enhanced. Adequately powered randomized controlled trials are needed to address efficacy, identify predictors of treatment outcome, and to assess the use of intranasal oxytocin within appropriate PTSD populations.
Literatur
1.
Zurück zum Zitat Kessler RC, Petukhova M, Sampson NA, Zaslavsky AM, Wittchen HU. Twelve-month and lifetime prevalence and lifetime morbid risk of anxiety and mood disorders in the United States. Int J Methods Psychiatr Res. 2012;21:169–84.CrossRefPubMedPubMedCentral Kessler RC, Petukhova M, Sampson NA, Zaslavsky AM, Wittchen HU. Twelve-month and lifetime prevalence and lifetime morbid risk of anxiety and mood disorders in the United States. Int J Methods Psychiatr Res. 2012;21:169–84.CrossRefPubMedPubMedCentral
2.
Zurück zum Zitat Tanielian T, Haycox LH, Schell TL, Marshall GN, Burnam MA, Eibner C, et al. Invisible wounds of war. Summary and recommendations for addressing psychological and cognitive injuries. DTIC Document; 2008. Tanielian T, Haycox LH, Schell TL, Marshall GN, Burnam MA, Eibner C, et al. Invisible wounds of war. Summary and recommendations for addressing psychological and cognitive injuries. DTIC Document; 2008.
3.
Zurück zum Zitat Pietrzak RH, Goldstein RB, Southwick SM, Grant BF. Prevalence and axis I comorbidity of full and partial posttraumatic stress disorder in the United States: results from Wave 2 of the National Epidemiologic Survey on Alcohol and Related Conditions. J Anxiety Disord. 2011;25(3):456–65.CrossRefPubMed Pietrzak RH, Goldstein RB, Southwick SM, Grant BF. Prevalence and axis I comorbidity of full and partial posttraumatic stress disorder in the United States: results from Wave 2 of the National Epidemiologic Survey on Alcohol and Related Conditions. J Anxiety Disord. 2011;25(3):456–65.CrossRefPubMed
4.
Zurück zum Zitat Petrakis IL, Rosenheck R, Desai R. Substance use comorbidity among veterans with posttraumatic stress disorder and other psychiatric illness. Am J Addict. 2011;20(3):185–9.CrossRefPubMed Petrakis IL, Rosenheck R, Desai R. Substance use comorbidity among veterans with posttraumatic stress disorder and other psychiatric illness. Am J Addict. 2011;20(3):185–9.CrossRefPubMed
5.
Zurück zum Zitat Kilmer B, Eibner C, Ringel JS, Pacula RL. Invisible wounds, visible savings? Using microsimulation to estimate the costs and savings associated with providing evidence-based treatment for PTSD and depression to veterans of Operation Enduring Freedom and Operation Iraqi Freedom. Psychol Trauma Theory Res Pract Policy. 2011;3(2):201–11.CrossRef Kilmer B, Eibner C, Ringel JS, Pacula RL. Invisible wounds, visible savings? Using microsimulation to estimate the costs and savings associated with providing evidence-based treatment for PTSD and depression to veterans of Operation Enduring Freedom and Operation Iraqi Freedom. Psychol Trauma Theory Res Pract Policy. 2011;3(2):201–11.CrossRef
6.
Zurück zum Zitat Kehle-Forbes SM, Meis LA, Spoont MR, Polusny MA. Treatment initiation and dropout from prolonged exposure and cognitive processing therapy in a VA outpatient clinic. Psychol Trauma Theory Res Pract Policy. 2016;8(1):107–14.CrossRef Kehle-Forbes SM, Meis LA, Spoont MR, Polusny MA. Treatment initiation and dropout from prolonged exposure and cognitive processing therapy in a VA outpatient clinic. Psychol Trauma Theory Res Pract Policy. 2016;8(1):107–14.CrossRef
7.
Zurück zum Zitat Hembree EA, Foa EB, Dorfan NM, Street GP, Kowalski J, Tu X. Do patients drop out prematurely from exposure therapy for PTSD? J Trauma Stress. 2003;16(6):555–62.CrossRefPubMed Hembree EA, Foa EB, Dorfan NM, Street GP, Kowalski J, Tu X. Do patients drop out prematurely from exposure therapy for PTSD? J Trauma Stress. 2003;16(6):555–62.CrossRefPubMed
8.
Zurück zum Zitat Bradley R, Greene J, Russ E, Dutra L, Westen D. A multidimensional meta-analysis of psychotherapy for PTSD. Am J Psychiatr. 2005;162:214–27.CrossRefPubMed Bradley R, Greene J, Russ E, Dutra L, Westen D. A multidimensional meta-analysis of psychotherapy for PTSD. Am J Psychiatr. 2005;162:214–27.CrossRefPubMed
9.
Zurück zum Zitat Bisson JI, Roberts NP, Andrew M, Cooper R, Lewis C. Psychological therapies for chronic post-traumatic stress disorder (PTSD) in adults. Cochrane Libr. 2013. Bisson JI, Roberts NP, Andrew M, Cooper R, Lewis C. Psychological therapies for chronic post-traumatic stress disorder (PTSD) in adults. Cochrane Libr. 2013.
10.
Zurück zum Zitat Schnurr PP, Lunney CA. Residual symptoms following prolonged exposure and present-centered therapy for PTSD in female veterans and soldiers. Depress Anxiety. 2019;36(2):162–9.CrossRefPubMed Schnurr PP, Lunney CA. Residual symptoms following prolonged exposure and present-centered therapy for PTSD in female veterans and soldiers. Depress Anxiety. 2019;36(2):162–9.CrossRefPubMed
11.
Zurück zum Zitat Larsen SE, Fleming CJ, Resick PA. Residual symptoms following empirically supported treatment for PTSD. Psychol Trauma Theory Res Pract Policy. 2019;11(2):207.CrossRef Larsen SE, Fleming CJ, Resick PA. Residual symptoms following empirically supported treatment for PTSD. Psychol Trauma Theory Res Pract Policy. 2019;11(2):207.CrossRef
12.
Zurück zum Zitat Krystal JH, Davis LL, Neylan TC, Raskind MA, Schnurr PP, Stein MB, et al. It is time to address the crisis in the pharmacotherapy of posttraumatic stress disorder: a consensus statement of the PTSD Psychopharmacology Working Group. Biol Psychiatry. 2017;82(7):e51–e9.CrossRefPubMed Krystal JH, Davis LL, Neylan TC, Raskind MA, Schnurr PP, Stein MB, et al. It is time to address the crisis in the pharmacotherapy of posttraumatic stress disorder: a consensus statement of the PTSD Psychopharmacology Working Group. Biol Psychiatry. 2017;82(7):e51–e9.CrossRefPubMed
13.
Zurück zum Zitat Olff M, Langeland W, Witteveen A, Denys D. A psychobiological rationale for oxytocin in the treatment of posttraumatic stress disorder. CNS Spectr. 2010;15(8):522–30.CrossRefPubMed Olff M, Langeland W, Witteveen A, Denys D. A psychobiological rationale for oxytocin in the treatment of posttraumatic stress disorder. CNS Spectr. 2010;15(8):522–30.CrossRefPubMed
14.
Zurück zum Zitat Eskandarian S, Vafaei AA, Vaezi GH, Taherian F, Kashefi A, Rashidy-Pour A. Effects of systemic administration of oxytocin on contextual fear extinction in a rat model of post-traumatic stress disorder. Basic Clin Neurosci. 2013;4(4):315.PubMedPubMedCentral Eskandarian S, Vafaei AA, Vaezi GH, Taherian F, Kashefi A, Rashidy-Pour A. Effects of systemic administration of oxytocin on contextual fear extinction in a rat model of post-traumatic stress disorder. Basic Clin Neurosci. 2013;4(4):315.PubMedPubMedCentral
15.
Zurück zum Zitat Missig G, Ayers LW, Schulkin J, Rosen JB. Oxytocin reduces background anxiety in a fear-potentiated startle paradigm. Neuropsychopharmacology. 2010;35(13):2607–16.CrossRefPubMedPubMedCentral Missig G, Ayers LW, Schulkin J, Rosen JB. Oxytocin reduces background anxiety in a fear-potentiated startle paradigm. Neuropsychopharmacology. 2010;35(13):2607–16.CrossRefPubMedPubMedCentral
16.
Zurück zum Zitat MacDonald K, MacDonald TM. The peptide that binds: a systematic review of oxytocin and its prosocial effects in humans. Harv Rev Psychiatry. 2010;18(1):1–21.CrossRefPubMed MacDonald K, MacDonald TM. The peptide that binds: a systematic review of oxytocin and its prosocial effects in humans. Harv Rev Psychiatry. 2010;18(1):1–21.CrossRefPubMed
17.
Zurück zum Zitat Acheson D, Feifel D, de Wilde S, Mckinney R, Lohr J, Risbrough V. The effect of intranasal oxytocin treatment on conditioned fear extinction and recall in a healthy human sample. Psychopharmacology. 2013;229(1):199–208.CrossRefPubMedPubMedCentral Acheson D, Feifel D, de Wilde S, Mckinney R, Lohr J, Risbrough V. The effect of intranasal oxytocin treatment on conditioned fear extinction and recall in a healthy human sample. Psychopharmacology. 2013;229(1):199–208.CrossRefPubMedPubMedCentral
18.
Zurück zum Zitat Koch S, van Zuiden M, Nawijn L, Frijling JL, Veltman DJ, Olff M. Intranasal oxytocin as strategy for medication-enhanced psychotherapy of PTSD: salience processing and fear inhibition processes. Psychoneuroendocrinology. 2014;40:242–56.CrossRefPubMed Koch S, van Zuiden M, Nawijn L, Frijling JL, Veltman DJ, Olff M. Intranasal oxytocin as strategy for medication-enhanced psychotherapy of PTSD: salience processing and fear inhibition processes. Psychoneuroendocrinology. 2014;40:242–56.CrossRefPubMed
19.
Zurück zum Zitat Lancaster CL, Teeters JB, Gros DF, Back SE. Posttraumatic stress disorder: overview of evidence-based assessment and treatment. J Clin Med. 2016;5:11.CrossRef Lancaster CL, Teeters JB, Gros DF, Back SE. Posttraumatic stress disorder: overview of evidence-based assessment and treatment. J Clin Med. 2016;5:11.CrossRef
20.
Zurück zum Zitat The Management of Posttraumatic Stress Disorder Work Group. VA/DoD clinical practice guideline for the management of posttraumatic stress disorder and acute stress disorder. Washington, D.C.; 2017. The Management of Posttraumatic Stress Disorder Work Group. VA/DoD clinical practice guideline for the management of posttraumatic stress disorder and acute stress disorder. Washington, D.C.; 2017.
21.
Zurück zum Zitat Resick PA, Monson CM, Chard KM. Cognitive processing therapy for PTSD: a comprehensive manual: Guilford Publications; 2016. Resick PA, Monson CM, Chard KM. Cognitive processing therapy for PTSD: a comprehensive manual: Guilford Publications; 2016.
22.
Zurück zum Zitat Shapiro F. Eye movement desensitization and reprocessing: basic principles, protocols, and procedures. New York: Guilford Press; 1995. Shapiro F. Eye movement desensitization and reprocessing: basic principles, protocols, and procedures. New York: Guilford Press; 1995.
23.
Zurück zum Zitat Davidson JT, Rothbaum BO, van der Kolk BA, Sikes CR, Farfel GM. Multicenter, double-blind comparison of sertraline and placebo in the treatment of posttraumatic stress disorder. Arch Gen Psychiatry. 2001;58(5):485–92.CrossRefPubMed Davidson JT, Rothbaum BO, van der Kolk BA, Sikes CR, Farfel GM. Multicenter, double-blind comparison of sertraline and placebo in the treatment of posttraumatic stress disorder. Arch Gen Psychiatry. 2001;58(5):485–92.CrossRefPubMed
24.
Zurück zum Zitat Stein DJ, Ipser J, McAnda N. Pharmacotherapy of posttraumatic stress disorder: a review of meta-analyses and treatment guidelines. CNS Spectr. 2009;14(1):25–31.CrossRefPubMed Stein DJ, Ipser J, McAnda N. Pharmacotherapy of posttraumatic stress disorder: a review of meta-analyses and treatment guidelines. CNS Spectr. 2009;14(1):25–31.CrossRefPubMed
25.
Zurück zum Zitat Friedman MJ, Marmar CR, Baker DG, Sikes CR, Farfel GM. Randomized, double-blind comparison of sertraline and placebo for posttraumatic stress disorder in a Department of Veterans Affairs setting. J Clin Psychiatry. 2007;68:711–20.CrossRefPubMed Friedman MJ, Marmar CR, Baker DG, Sikes CR, Farfel GM. Randomized, double-blind comparison of sertraline and placebo for posttraumatic stress disorder in a Department of Veterans Affairs setting. J Clin Psychiatry. 2007;68:711–20.CrossRefPubMed
26.
Zurück zum Zitat Hetrick SE, Purcell R, Garner B, Parslow R. Combined pharmacotherapy and psychological therapies for post traumatic stress disorder (PTSD). Cochrane Database Syst Rev 2010;7(7). Hetrick SE, Purcell R, Garner B, Parslow R. Combined pharmacotherapy and psychological therapies for post traumatic stress disorder (PTSD). Cochrane Database Syst Rev 2010;7(7).
27.
Zurück zum Zitat Rauch SA, Kim HM, Powell C, Tuerk PW, Simon NM, Acierno R, et al. Efficacy of prolonged exposure therapy, sertraline hydrochloride, and their combination among combat veterans with posttraumatic stress disorder: a randomized clinical trial. JAMA Psychiatry 2018. Rauch SA, Kim HM, Powell C, Tuerk PW, Simon NM, Acierno R, et al. Efficacy of prolonged exposure therapy, sertraline hydrochloride, and their combination among combat veterans with posttraumatic stress disorder: a randomized clinical trial. JAMA Psychiatry 2018.
28.
Zurück zum Zitat Raskind MA, Peskind ER, Chow B, Harris C, Davis-Karim A, Holmes HA, et al. Trial of prazosin for post-traumatic stress disorder in military veterans. N Engl J Med. 2018;378(6):507–17.CrossRefPubMed Raskind MA, Peskind ER, Chow B, Harris C, Davis-Karim A, Holmes HA, et al. Trial of prazosin for post-traumatic stress disorder in military veterans. N Engl J Med. 2018;378(6):507–17.CrossRefPubMed
29.
Zurück zum Zitat Raskind MA, Peskind ER, Hoff DJ, Hart KL, Holmes HA, Warren D, et al. A parallel group placebo controlled study of prazosin for trauma nightmares and sleep disturbance in combat veterans with post-traumatic stress disorder. Biol Psychiatry. 2007;61(8):928–34.CrossRefPubMed Raskind MA, Peskind ER, Hoff DJ, Hart KL, Holmes HA, Warren D, et al. A parallel group placebo controlled study of prazosin for trauma nightmares and sleep disturbance in combat veterans with post-traumatic stress disorder. Biol Psychiatry. 2007;61(8):928–34.CrossRefPubMed
30.
Zurück zum Zitat Simpson TL, Malte CA, Dietel B, Tell D, Pocock I, Lyons R, et al. A pilot trial of prazosin, an alpha-1 adrenergic antagonist, for comorbid alcohol dependence and posttraumatic stress disorder. Alcohol Clin Exp Res. 2015;39(5):808–17.CrossRefPubMedPubMedCentral Simpson TL, Malte CA, Dietel B, Tell D, Pocock I, Lyons R, et al. A pilot trial of prazosin, an alpha-1 adrenergic antagonist, for comorbid alcohol dependence and posttraumatic stress disorder. Alcohol Clin Exp Res. 2015;39(5):808–17.CrossRefPubMedPubMedCentral
31.
Zurück zum Zitat Germain A, Richardson R, Moul DE. Placebo-controlled comparison of prazosin and cognitive-behavioral treatments for sleep disturbances in US military veterans. J Psychosom Res. 2012;72:89–96.CrossRefPubMed Germain A, Richardson R, Moul DE. Placebo-controlled comparison of prazosin and cognitive-behavioral treatments for sleep disturbances in US military veterans. J Psychosom Res. 2012;72:89–96.CrossRefPubMed
32.
Zurück zum Zitat Raskind MA, Peterson K, Williams T, Hoff DJ, Hart KL, Holmes HA, et al. A trial of prazosin for combat trauma PTSD with nightmares in active-duty soldiers returned from Iraq and Afghanistan. Am J Psychiatr. 2013;170(9):1003–10.CrossRefPubMed Raskind MA, Peterson K, Williams T, Hoff DJ, Hart KL, Holmes HA, et al. A trial of prazosin for combat trauma PTSD with nightmares in active-duty soldiers returned from Iraq and Afghanistan. Am J Psychiatr. 2013;170(9):1003–10.CrossRefPubMed
33.
Zurück zum Zitat Kida S. Reconsolidation/destabilization, extinction and forgetting of fear memory as therapeutic targets for PTSD. Psychopharmacology. 2018;236(1):49–57.CrossRefPubMedPubMedCentral Kida S. Reconsolidation/destabilization, extinction and forgetting of fear memory as therapeutic targets for PTSD. Psychopharmacology. 2018;236(1):49–57.CrossRefPubMedPubMedCentral
34.
Zurück zum Zitat Maples-Keller JL, Jovanovic T, Dunlop BW, Rauch SA, Yasinski C, Michopoulos V, et al. When translational neuroscience fails in the clinic: dexamethasone prior to virtual reality exposure therapy increases drop-out rates. J Anxiety Disord. 2019;61:89–97.CrossRefPubMed Maples-Keller JL, Jovanovic T, Dunlop BW, Rauch SA, Yasinski C, Michopoulos V, et al. When translational neuroscience fails in the clinic: dexamethasone prior to virtual reality exposure therapy increases drop-out rates. J Anxiety Disord. 2019;61:89–97.CrossRefPubMed
35.
Zurück zum Zitat Bentz D, Michael T, Dominique J, Wilhelm FH. Enhancing exposure therapy for anxiety disorders with glucocorticoids: from basic mechanisms of emotional learning to clinical applications. J Anxiety Disord. 2010;24(2):223–30.CrossRefPubMed Bentz D, Michael T, Dominique J, Wilhelm FH. Enhancing exposure therapy for anxiety disorders with glucocorticoids: from basic mechanisms of emotional learning to clinical applications. J Anxiety Disord. 2010;24(2):223–30.CrossRefPubMed
36.
Zurück zum Zitat Otto MW, McHugh RK, Kantak KM. Combined pharmacotherapy and cognitive-behavioral therapy for anxiety disorders: medication effects, glucocorticoids, and attenuated treatment outcomes. Clin Psychol Sci Pract. 2010;17(2):91–103.CrossRef Otto MW, McHugh RK, Kantak KM. Combined pharmacotherapy and cognitive-behavioral therapy for anxiety disorders: medication effects, glucocorticoids, and attenuated treatment outcomes. Clin Psychol Sci Pract. 2010;17(2):91–103.CrossRef
37.
Zurück zum Zitat Yehuda R, Bierer LM, Pratchett LC, Lehrner A, Koch EC, Van Manen JA, et al. Cortisol augmentation of a psychological treatment for warfighters with posttraumatic stress disorder: randomized trial showing improved treatment retention and outcome. Psychoneuroendocrinology. 2015;51:589–97.CrossRefPubMed Yehuda R, Bierer LM, Pratchett LC, Lehrner A, Koch EC, Van Manen JA, et al. Cortisol augmentation of a psychological treatment for warfighters with posttraumatic stress disorder: randomized trial showing improved treatment retention and outcome. Psychoneuroendocrinology. 2015;51:589–97.CrossRefPubMed
38.
Zurück zum Zitat Litz BT, Salters-Pedneault K, Steenkamp MM, Hermos JA, Bryant RA, Otto MW, et al. A randomized placebo-controlled trial of D-cycloserine and exposure therapy for posttraumatic stress disorder. J Psychiatr Res. 2012;46(9):1184–90.CrossRefPubMed Litz BT, Salters-Pedneault K, Steenkamp MM, Hermos JA, Bryant RA, Otto MW, et al. A randomized placebo-controlled trial of D-cycloserine and exposure therapy for posttraumatic stress disorder. J Psychiatr Res. 2012;46(9):1184–90.CrossRefPubMed
39.
Zurück zum Zitat Mithoefer MC, Mithoefer AT, Feduccia AA, Jerome L, Wagner M, Wymer J, et al. 3,4-Methylenedioxymethamphetamine (MDMA)-assisted psychotherapy for post-traumatic stress disorder in military veterans, firefighters, and police officers: a randomised, double-blind, dose-response, phase 2 clinical trial. Lancet Psychiatry. 2018;5(6):486–97.CrossRefPubMed Mithoefer MC, Mithoefer AT, Feduccia AA, Jerome L, Wagner M, Wymer J, et al. 3,4-Methylenedioxymethamphetamine (MDMA)-assisted psychotherapy for post-traumatic stress disorder in military veterans, firefighters, and police officers: a randomised, double-blind, dose-response, phase 2 clinical trial. Lancet Psychiatry. 2018;5(6):486–97.CrossRefPubMed
40.
Zurück zum Zitat Mataix-Cols D, De La Cruz LF, Monzani B, Rosenfield D, Andersson E, Pérez-Vigil A, et al. D-cycloserine augmentation of exposure-based cognitive behavior therapy for anxiety, obsessive-compulsive, and posttraumatic stress disorders: a systematic review and meta-analysis of individual participant data. JAMA Psychiatry. 2017;74(5):501–10.CrossRefPubMed Mataix-Cols D, De La Cruz LF, Monzani B, Rosenfield D, Andersson E, Pérez-Vigil A, et al. D-cycloserine augmentation of exposure-based cognitive behavior therapy for anxiety, obsessive-compulsive, and posttraumatic stress disorders: a systematic review and meta-analysis of individual participant data. JAMA Psychiatry. 2017;74(5):501–10.CrossRefPubMed
41.
Zurück zum Zitat Tuerk PW, Wangelin BC, Powers MB, Smits J, Acierno R, Myers US, et al. Augmenting treatment efficiency in exposure therapy for PTSD: a randomized double-blind placebo-controlled trial of yohimbine HCl. Cogn Behav Ther 2018:1–21. Tuerk PW, Wangelin BC, Powers MB, Smits J, Acierno R, Myers US, et al. Augmenting treatment efficiency in exposure therapy for PTSD: a randomized double-blind placebo-controlled trial of yohimbine HCl. Cogn Behav Ther 2018:1–21.
42.
Zurück zum Zitat Rauch SA, Koola C, Post L, Yasinski C, Norrholm SD, Black K, et al. In session extinction and outcome in virtual reality exposure therapy for PTSD. Behav Res Ther. 2018;109:1–9.CrossRefPubMed Rauch SA, Koola C, Post L, Yasinski C, Norrholm SD, Black K, et al. In session extinction and outcome in virtual reality exposure therapy for PTSD. Behav Res Ther. 2018;109:1–9.CrossRefPubMed
43.
Zurück zum Zitat • Flanagan JC, Sippel LM, Wahlquist A, Moran-Santa Maria MM, Back SE. Augmenting prolonged exposure therapy for PTSD with intranasal oxytocin: a randomized, placebo-controlled pilot trial. J Psychiatr Res. 2017;98:64–9 The first randomized controlled study to examine oxytocin combined with behavioral PTSD treatment.CrossRefPubMedPubMedCentral • Flanagan JC, Sippel LM, Wahlquist A, Moran-Santa Maria MM, Back SE. Augmenting prolonged exposure therapy for PTSD with intranasal oxytocin: a randomized, placebo-controlled pilot trial. J Psychiatr Res. 2017;98:64–9 The first randomized controlled study to examine oxytocin combined with behavioral PTSD treatment.CrossRefPubMedPubMedCentral
44.
Zurück zum Zitat Frijling JL, Zuiden M, Nawijn L, Koch S, Neumann ID, Veltman DJ, et al. Salivary oxytocin and vasopressin levels in police officers with and without post-traumatic stress disorder. J Neuroendocrinol. 2015;27(10):743–51.CrossRefPubMed Frijling JL, Zuiden M, Nawijn L, Koch S, Neumann ID, Veltman DJ, et al. Salivary oxytocin and vasopressin levels in police officers with and without post-traumatic stress disorder. J Neuroendocrinol. 2015;27(10):743–51.CrossRefPubMed
45.
Zurück zum Zitat Reijnen A, Geuze E, Vermetten E. Individual variation in plasma oxytocin and vasopressin levels in relation to the development of combat-related PTSD in a large military cohort. J Psychiatr Res. 2017;94:88–95.CrossRefPubMed Reijnen A, Geuze E, Vermetten E. Individual variation in plasma oxytocin and vasopressin levels in relation to the development of combat-related PTSD in a large military cohort. J Psychiatr Res. 2017;94:88–95.CrossRefPubMed
46.
Zurück zum Zitat Sippel LM, Han S, Watkins LE, Harpaz-Rotem I, Southwick SM, Krystal JH, et al. Oxytocin receptor gene polymorphisms, attachment, and PTSD: results from the National Health and Resilience in Veterans Study. J Psychiatr Res. 2017;94:139–47.CrossRefPubMedPubMedCentral Sippel LM, Han S, Watkins LE, Harpaz-Rotem I, Southwick SM, Krystal JH, et al. Oxytocin receptor gene polymorphisms, attachment, and PTSD: results from the National Health and Resilience in Veterans Study. J Psychiatr Res. 2017;94:139–47.CrossRefPubMedPubMedCentral
47.
Zurück zum Zitat Guastella AJ, Hickie IB, McGuinness MM, Otis M, Woods EA, Disinger HM, et al. Recommendations for the standardisation of oxytocin nasal administration and guidelines for its reporting in human research. Psychoneuroendocrinology. 2013;38(5):612–25.CrossRefPubMed Guastella AJ, Hickie IB, McGuinness MM, Otis M, Woods EA, Disinger HM, et al. Recommendations for the standardisation of oxytocin nasal administration and guidelines for its reporting in human research. Psychoneuroendocrinology. 2013;38(5):612–25.CrossRefPubMed
48.
Zurück zum Zitat Milewski M, Goodey A, Lee DJ, Rimmer E, Saklatvala R, Koyama S, et al. Rapid absorption of dry-powder intranasal oxytocin. Pharm Res. 2016;33(8):1936–44.CrossRefPubMed Milewski M, Goodey A, Lee DJ, Rimmer E, Saklatvala R, Koyama S, et al. Rapid absorption of dry-powder intranasal oxytocin. Pharm Res. 2016;33(8):1936–44.CrossRefPubMed
49.
Zurück zum Zitat Quintana DS, Westlye LT, Hope S, Nærland T, Elvsåshagen T, Dørum E, et al. Dose-dependent social-cognitive effects of intranasal oxytocin delivered with novel Breath Powered device in adults with autism spectrum disorder: a randomized placebo-controlled double-blind crossover trial. Transl Psychiatry. 2017;7(5):e1136.CrossRefPubMedPubMedCentral Quintana DS, Westlye LT, Hope S, Nærland T, Elvsåshagen T, Dørum E, et al. Dose-dependent social-cognitive effects of intranasal oxytocin delivered with novel Breath Powered device in adults with autism spectrum disorder: a randomized placebo-controlled double-blind crossover trial. Transl Psychiatry. 2017;7(5):e1136.CrossRefPubMedPubMedCentral
50.
Zurück zum Zitat Olff M, Frijling JL, Kubzansky LD, Bradley B, Ellenbogen MA, Cardoso C, et al. The role of oxytocin in social bonding, stress regulation and mental health: an update on the moderating effects of context and interindividual differences. Psychoneuroendocrinology. 2013;38(9):1883–94.CrossRefPubMed Olff M, Frijling JL, Kubzansky LD, Bradley B, Ellenbogen MA, Cardoso C, et al. The role of oxytocin in social bonding, stress regulation and mental health: an update on the moderating effects of context and interindividual differences. Psychoneuroendocrinology. 2013;38(9):1883–94.CrossRefPubMed
51.
Zurück zum Zitat Bartz JA, Zaki J, Bolger N, Ochsner KN. Social effects of oxytocin in humans: context and person matter. Trends Cogn Sci. 2011;15(7):301–9.PubMed Bartz JA, Zaki J, Bolger N, Ochsner KN. Social effects of oxytocin in humans: context and person matter. Trends Cogn Sci. 2011;15(7):301–9.PubMed
52.
Zurück zum Zitat Mitchell JM, Arcuni PA, Weinstein D, Woolley JD. Intranasal oxytocin selectively modulates social perception, craving, and approach behavior in subjects with alcohol use disorder. J Addict Med. 2016;10(3):182–9.CrossRefPubMed Mitchell JM, Arcuni PA, Weinstein D, Woolley JD. Intranasal oxytocin selectively modulates social perception, craving, and approach behavior in subjects with alcohol use disorder. J Addict Med. 2016;10(3):182–9.CrossRefPubMed
53.
Zurück zum Zitat Ebner NC, Lin T, Muradoglu M, Weir DH, Plasencia GM, Lillard TS, et al. Associations between oxytocin receptor gene (OXTR) methylation, plasma oxytocin, and attachment across adulthood. Int J Psychophysiol. 2019;136:22–32.CrossRefPubMed Ebner NC, Lin T, Muradoglu M, Weir DH, Plasencia GM, Lillard TS, et al. Associations between oxytocin receptor gene (OXTR) methylation, plasma oxytocin, and attachment across adulthood. Int J Psychophysiol. 2019;136:22–32.CrossRefPubMed
54.
Zurück zum Zitat •• Shamay-Tsoory SG, Abu-Akel A. The social salience hypothesis of oxytocin. Biol Psychiatry. 2016;79(3):194–202 Excellent review consolidating and explaining inconsistent findings in clinical oxytocin research.CrossRefPubMed •• Shamay-Tsoory SG, Abu-Akel A. The social salience hypothesis of oxytocin. Biol Psychiatry. 2016;79(3):194–202 Excellent review consolidating and explaining inconsistent findings in clinical oxytocin research.CrossRefPubMed
55.
Zurück zum Zitat MacDonald E, Dadds MR, Brennan JL, Williams K, Levy F, Cauchi AJ. A review of safety, side-effects and subjective reactions to intranasal oxytocin in human research. Psychoneuroendocrinology. 2011;36(8):1114–26.CrossRefPubMed MacDonald E, Dadds MR, Brennan JL, Williams K, Levy F, Cauchi AJ. A review of safety, side-effects and subjective reactions to intranasal oxytocin in human research. Psychoneuroendocrinology. 2011;36(8):1114–26.CrossRefPubMed
57.
Zurück zum Zitat Xu H, Fu S, Chen Q, Gu M, Zhou J, Liu C, et al. The function of oxytocin: a potential biomarker for prostate cancer diagnosis and promoter of prostate cancer. Oncotarget. 2017;8(19):312–5. Xu H, Fu S, Chen Q, Gu M, Zhou J, Liu C, et al. The function of oxytocin: a potential biomarker for prostate cancer diagnosis and promoter of prostate cancer. Oncotarget. 2017;8(19):312–5.
58.
Zurück zum Zitat Weisman O, Zagoory-Sharon O, Schneiderman I, Gordon I, Feldman R. Plasma oxytocin distributions in a large cohort of women and men and their gender-specific associations with anxiety. Psychoneuroendocrinology. 2013;38(5):694–701.CrossRefPubMed Weisman O, Zagoory-Sharon O, Schneiderman I, Gordon I, Feldman R. Plasma oxytocin distributions in a large cohort of women and men and their gender-specific associations with anxiety. Psychoneuroendocrinology. 2013;38(5):694–701.CrossRefPubMed
59.
Zurück zum Zitat Loth E, Poline JB, Thyreau B, Jia T, Tao C, Lourdusamy A, et al. Oxytocin receptor genotype modulates ventral striatal activity to social cues and response to stressful life events. Biol Psychiatry 2013. Loth E, Poline JB, Thyreau B, Jia T, Tao C, Lourdusamy A, et al. Oxytocin receptor genotype modulates ventral striatal activity to social cues and response to stressful life events. Biol Psychiatry 2013.
60.
Zurück zum Zitat Eckstein M, Becker B, Scheele D, Scholz C, Preckel K, Schlaepfer TE, et al. Oxytocin facilitates the extinction of conditioned fear in humans. Biol Psychiatry. 2014;78(3):194–202.CrossRefPubMed Eckstein M, Becker B, Scheele D, Scholz C, Preckel K, Schlaepfer TE, et al. Oxytocin facilitates the extinction of conditioned fear in humans. Biol Psychiatry. 2014;78(3):194–202.CrossRefPubMed
61.
Zurück zum Zitat Ellenbogen MA, Linnen A, Cardoso C, Joober R. Intranasal oxytocin attenuates the human acoustic startle response independent of emotional modulation. Psychophysiology. 2014;51(11):1169–77.CrossRefPubMed Ellenbogen MA, Linnen A, Cardoso C, Joober R. Intranasal oxytocin attenuates the human acoustic startle response independent of emotional modulation. Psychophysiology. 2014;51(11):1169–77.CrossRefPubMed
62.
Zurück zum Zitat Bertsch K, Gamer M, Schmidt B, Schmidinger I, Walther S, Kästel T, et al. Oxytocin and reduction of social threat hypersensitivity in women with borderline personality disorder. Am J Psychiatr. 2013;170(10):1169–77.CrossRefPubMed Bertsch K, Gamer M, Schmidt B, Schmidinger I, Walther S, Kästel T, et al. Oxytocin and reduction of social threat hypersensitivity in women with borderline personality disorder. Am J Psychiatr. 2013;170(10):1169–77.CrossRefPubMed
63.
Zurück zum Zitat Kosfeld M, Heinrichs M, Zak PJ, Fischbacher U, Fehr E. Oxytocin increases trust in humans. Nature. 2005;435(7042):673–6.CrossRefPubMed Kosfeld M, Heinrichs M, Zak PJ, Fischbacher U, Fehr E. Oxytocin increases trust in humans. Nature. 2005;435(7042):673–6.CrossRefPubMed
64.
Zurück zum Zitat Gibbons CJ, Nich C, Steinberg K, Roffman RA, Corvino J, Babor TF, et al. Treatment process, alliance and outcome in brief versus extended treatments for marijuana dependence. Addiction. 2010;105(10):1799–808.CrossRefPubMedPubMedCentral Gibbons CJ, Nich C, Steinberg K, Roffman RA, Corvino J, Babor TF, et al. Treatment process, alliance and outcome in brief versus extended treatments for marijuana dependence. Addiction. 2010;105(10):1799–808.CrossRefPubMedPubMedCentral
65.
Zurück zum Zitat • van Zuiden M, Frijling JL, Nawijn L, Koch S, Goslings JC, Luitse JS, et al. Intranasal oxytocin to prevent PTSD symptoms: a randomized controlled trial in emergency department patients. Biol Psychiatry. 2016;81(12):1030–40 First study to examine a repeated dosing strategy to prevent PTSD onset.CrossRefPubMed • van Zuiden M, Frijling JL, Nawijn L, Koch S, Goslings JC, Luitse JS, et al. Intranasal oxytocin to prevent PTSD symptoms: a randomized controlled trial in emergency department patients. Biol Psychiatry. 2016;81(12):1030–40 First study to examine a repeated dosing strategy to prevent PTSD onset.CrossRefPubMed
66.
Zurück zum Zitat Dunlop B, Mansson E, Gerardi M. Pharmacological innovations for posttraumatic stress disorder and medication-enhanced psychotherapy. Curr Pharm Des. 2012;18(35):5645–58.CrossRefPubMed Dunlop B, Mansson E, Gerardi M. Pharmacological innovations for posttraumatic stress disorder and medication-enhanced psychotherapy. Curr Pharm Des. 2012;18(35):5645–58.CrossRefPubMed
67.
Zurück zum Zitat Domes G, Heinrichs M, Glascher J, Buchel C, Braus DF, Herpertz SC. Oxytocin attenuates amygdala responses to emotional faces regardless of valence. Biol Psychiatry. 2007;62:1187–90.CrossRefPubMed Domes G, Heinrichs M, Glascher J, Buchel C, Braus DF, Herpertz SC. Oxytocin attenuates amygdala responses to emotional faces regardless of valence. Biol Psychiatry. 2007;62:1187–90.CrossRefPubMed
68.
Zurück zum Zitat Sripada CS, Phan KL, Labuschagne I, Welsh RC, Nathan PJ, Wood AG. Oxytocin enhances resting-state connectivity between amygdala and medial frontal cortex. Int J Neuropsychopharmacol. 2013;16(2):255–60.CrossRefPubMed Sripada CS, Phan KL, Labuschagne I, Welsh RC, Nathan PJ, Wood AG. Oxytocin enhances resting-state connectivity between amygdala and medial frontal cortex. Int J Neuropsychopharmacol. 2013;16(2):255–60.CrossRefPubMed
69.
Zurück zum Zitat Driessen M, Schulte S, Luedecke C, Schaefer I, Sutmann F, Ohlmeier M, et al. Trauma and PTSD in patients with alcohol, drug, or dual dependence: a multi-center study. Alcohol Clin Exp Res. 2008;32(3):481–8.CrossRefPubMed Driessen M, Schulte S, Luedecke C, Schaefer I, Sutmann F, Ohlmeier M, et al. Trauma and PTSD in patients with alcohol, drug, or dual dependence: a multi-center study. Alcohol Clin Exp Res. 2008;32(3):481–8.CrossRefPubMed
70.
Zurück zum Zitat Mills KL, Teesson M, Ross J, Peters L. Trauma, PTSD, and substance use disorders: findings from the Australian National Survey of Mental Health and Well-Being. Am J Psychiatr. 2006;163(4):652–8.CrossRefPubMed Mills KL, Teesson M, Ross J, Peters L. Trauma, PTSD, and substance use disorders: findings from the Australian National Survey of Mental Health and Well-Being. Am J Psychiatr. 2006;163(4):652–8.CrossRefPubMed
71.
Zurück zum Zitat Hien DA, Campbell A, Ruglass LM, Hu M, Killeen TK. The role of alcohol misuse in PTSD outcomes for women in community treatment: a secondary analysis of NIDA's Women and Trauma Study. Drug Alcohol Depend. 2010;111(1):114–9.CrossRefPubMedPubMedCentral Hien DA, Campbell A, Ruglass LM, Hu M, Killeen TK. The role of alcohol misuse in PTSD outcomes for women in community treatment: a secondary analysis of NIDA's Women and Trauma Study. Drug Alcohol Depend. 2010;111(1):114–9.CrossRefPubMedPubMedCentral
72.
Zurück zum Zitat Back SE. Toward an improved model of treating co-occurring PTSD and substance use disorders. Am J Psychiatr. 2010;167(1):11–3.CrossRefPubMed Back SE. Toward an improved model of treating co-occurring PTSD and substance use disorders. Am J Psychiatr. 2010;167(1):11–3.CrossRefPubMed
73.
Zurück zum Zitat Cohen LR, Hien DA. Treatment outcomes for women with substance abuse and PTSD who have experienced complex trauma. Psychiatr Serv. 2014;57(1):100–6.CrossRef Cohen LR, Hien DA. Treatment outcomes for women with substance abuse and PTSD who have experienced complex trauma. Psychiatr Serv. 2014;57(1):100–6.CrossRef
74.
Zurück zum Zitat Hien DA, Jiang H, Campbell ANC, Hu MC, Miele GM, Cohen LR, et al. Do treatment improvements in PTSD severity affect substance use outcomes? A secondary analysis from a randomized clinical trial in NIDA’s Clinical Trials Network. Am J Psychiatr. 2010;167(1):95.CrossRefPubMed Hien DA, Jiang H, Campbell ANC, Hu MC, Miele GM, Cohen LR, et al. Do treatment improvements in PTSD severity affect substance use outcomes? A secondary analysis from a randomized clinical trial in NIDA’s Clinical Trials Network. Am J Psychiatr. 2010;167(1):95.CrossRefPubMed
75.
Zurück zum Zitat Back SE, Waldrop AE, Brady KT. Treatment challenges associated with comorbid substance use and posttraumatic stress disorder: clinicians' perspectives. Am J Addict. 2009;18(1):15–20.CrossRefPubMedPubMedCentral Back SE, Waldrop AE, Brady KT. Treatment challenges associated with comorbid substance use and posttraumatic stress disorder: clinicians' perspectives. Am J Addict. 2009;18(1):15–20.CrossRefPubMedPubMedCentral
76.
Zurück zum Zitat Back SE, Brady KT, Sonne SC, Verduin ML. Symptom improvement in co-occurring PTSD and alcohol dependence. J Nerv Ment Dis. 2006;194(9):690–6.CrossRefPubMed Back SE, Brady KT, Sonne SC, Verduin ML. Symptom improvement in co-occurring PTSD and alcohol dependence. J Nerv Ment Dis. 2006;194(9):690–6.CrossRefPubMed
77.
Zurück zum Zitat Back SE, Waldrop AE, Brady KT, Hien D. Evidenced-based time-limited treatment of co-occurring substance-use disorders and civilian-related posttraumatic stress disorder. Brief Treat Crisis Interv. 2006;6(4):283.CrossRef Back SE, Waldrop AE, Brady KT, Hien D. Evidenced-based time-limited treatment of co-occurring substance-use disorders and civilian-related posttraumatic stress disorder. Brief Treat Crisis Interv. 2006;6(4):283.CrossRef
78.
Zurück zum Zitat Najavits LM, Weiss RD, Liese BS. Group cognitive-behavioral therapy for women with PTSD and substance use disorder. J Subst Abus Treat. 1996;13(1):13–22.CrossRef Najavits LM, Weiss RD, Liese BS. Group cognitive-behavioral therapy for women with PTSD and substance use disorder. J Subst Abus Treat. 1996;13(1):13–22.CrossRef
79.
Zurück zum Zitat Koob GF, Buck CL, Cohen A, Edwards S, Park PE, Schlosburg JE, et al. Addiction as a stress surfeit disorder. Neuropharmacology. 2014;76:370–82.CrossRefPubMed Koob GF, Buck CL, Cohen A, Edwards S, Park PE, Schlosburg JE, et al. Addiction as a stress surfeit disorder. Neuropharmacology. 2014;76:370–82.CrossRefPubMed
80.
Zurück zum Zitat Petrakis IL, Ralevski E, Desai N, Trevisan L, Gueorguieva R, Rounsaville B, et al. Noradrenergic vs serotonergic antidepressant with or without naltrexone for veterans with PTSD and comorbid alcohol dependence. Neuropsychopharmacology. 2012;37(4):996–1004.CrossRefPubMed Petrakis IL, Ralevski E, Desai N, Trevisan L, Gueorguieva R, Rounsaville B, et al. Noradrenergic vs serotonergic antidepressant with or without naltrexone for veterans with PTSD and comorbid alcohol dependence. Neuropsychopharmacology. 2012;37(4):996–1004.CrossRefPubMed
81.
Zurück zum Zitat Brady KT, Sinha R. Co-occurring mental and substance use disorders: the neurobiological effects of chronic stress. Am J Psychiatr. 2005;162(8):1483–93.CrossRefPubMed Brady KT, Sinha R. Co-occurring mental and substance use disorders: the neurobiological effects of chronic stress. Am J Psychiatr. 2005;162(8):1483–93.CrossRefPubMed
82.
Zurück zum Zitat Hien DA, Levin FR, Ruglass LM, López-Castro T, Papini S, Hu M, et al. Combining seeking safety with sertraline for PTSD and alcohol use disorders: a randomized controlled trial. J Consult Clin Psychol. 2015;83(2):359.CrossRefPubMedPubMedCentral Hien DA, Levin FR, Ruglass LM, López-Castro T, Papini S, Hu M, et al. Combining seeking safety with sertraline for PTSD and alcohol use disorders: a randomized controlled trial. J Consult Clin Psychol. 2015;83(2):359.CrossRefPubMedPubMedCentral
83.
Zurück zum Zitat Petrakis IL, Desai N, Gueorguieva R, Arias AJ, O'Brien E, Jane JS, et al. Prazosin for veterans with posttraumatic stress disorder and comorbid alcohol dependence: a clinical trial. Alcohol Clin Exp Res. 2016;40(1):178–86.CrossRefPubMed Petrakis IL, Desai N, Gueorguieva R, Arias AJ, O'Brien E, Jane JS, et al. Prazosin for veterans with posttraumatic stress disorder and comorbid alcohol dependence: a clinical trial. Alcohol Clin Exp Res. 2016;40(1):178–86.CrossRefPubMed
84.
Zurück zum Zitat Back SE, Flanagan JC, Jones JL, Augur I, Peterson AL, Young-McCaughan S, et al. Doxazosin for the treatment of co-occurring PTSD and alcohol use disorder: design and methodology of a randomized controlled trial in military veterans. Contemp Clin Trials. 2018;73:8–15.CrossRefPubMedPubMedCentral Back SE, Flanagan JC, Jones JL, Augur I, Peterson AL, Young-McCaughan S, et al. Doxazosin for the treatment of co-occurring PTSD and alcohol use disorder: design and methodology of a randomized controlled trial in military veterans. Contemp Clin Trials. 2018;73:8–15.CrossRefPubMedPubMedCentral
85.
Zurück zum Zitat Blodgett JC, Del Re AC, Maisel NC, Finney JW. A meta-analysis of topiramate's effects for individuals with alcohol use disorders. Alcohol Clin Exp Res. 2014;38(6):1481–8.CrossRefPubMedPubMedCentral Blodgett JC, Del Re AC, Maisel NC, Finney JW. A meta-analysis of topiramate's effects for individuals with alcohol use disorders. Alcohol Clin Exp Res. 2014;38(6):1481–8.CrossRefPubMedPubMedCentral
86.
Zurück zum Zitat Johnson BA, Ait-Daoud N, Wang X, Penberthy JK, Javors MA, Seneviratne C, et al. Topiramate for the treatment of cocaine addiction: a randomized clinical trial. JAMA Psychiatry. 2013;70(12):1338–46.CrossRefPubMed Johnson BA, Ait-Daoud N, Wang X, Penberthy JK, Javors MA, Seneviratne C, et al. Topiramate for the treatment of cocaine addiction: a randomized clinical trial. JAMA Psychiatry. 2013;70(12):1338–46.CrossRefPubMed
87.
Zurück zum Zitat Watts BV, Schnurr PP, Mayo L, Young-Xu Y, Weeks WB, Friedman MJ. Meta-analysis of the efficacy of treatments for posttraumatic stress disorder. J Clin Psychiatry. 2013;74(6):1,478–550.CrossRef Watts BV, Schnurr PP, Mayo L, Young-Xu Y, Weeks WB, Friedman MJ. Meta-analysis of the efficacy of treatments for posttraumatic stress disorder. J Clin Psychiatry. 2013;74(6):1,478–550.CrossRef
88.
Zurück zum Zitat Back SE, McCauley JL, Korte KJ, Gros DF, Leavitt V, Gray KM, et al. A double-blind randomized controlled pilot trial of N-acetylcysteine in veterans with PTSD and substance use disorders. J Clin Psychiatry. 2016;77(11):e1439–e46.CrossRefPubMedPubMedCentral Back SE, McCauley JL, Korte KJ, Gros DF, Leavitt V, Gray KM, et al. A double-blind randomized controlled pilot trial of N-acetylcysteine in veterans with PTSD and substance use disorders. J Clin Psychiatry. 2016;77(11):e1439–e46.CrossRefPubMedPubMedCentral
89.
Zurück zum Zitat Batki SL, Pennington DL, Lasher B, Neylan TC, Metzler T, Waldrop AE, et al. Topiramate treatment of alcohol use disorder in veterans with posttraumatic stress disorder: a randomized controlled pilot trial. Alcohol Clin Exp Res. 2014;38(8):2169–77.CrossRefPubMedPubMedCentral Batki SL, Pennington DL, Lasher B, Neylan TC, Metzler T, Waldrop AE, et al. Topiramate treatment of alcohol use disorder in veterans with posttraumatic stress disorder: a randomized controlled pilot trial. Alcohol Clin Exp Res. 2014;38(8):2169–77.CrossRefPubMedPubMedCentral
90.
Zurück zum Zitat McRae-Clark AL, Baker NL, Moran-Santa Maria M, Brady KT. Effect of oxytocin on craving and stress response in marijuana-dependent individuals: a pilot study. Psychopharmacology. 2013;228(4):1–9.CrossRef McRae-Clark AL, Baker NL, Moran-Santa Maria M, Brady KT. Effect of oxytocin on craving and stress response in marijuana-dependent individuals: a pilot study. Psychopharmacology. 2013;228(4):1–9.CrossRef
91.
Zurück zum Zitat Carson DS, Hunt GE, Guastella AJ, Barber L, Cornish JL, Arnold JC, et al. Systemically administered oxytocin decreases methamphetamine activation of the subthalamic nucleus and accumbens core and stimulates oxytocinergic neurons in the hypothalamus. Addict Biol. 2010;15(4):448–63.CrossRefPubMed Carson DS, Hunt GE, Guastella AJ, Barber L, Cornish JL, Arnold JC, et al. Systemically administered oxytocin decreases methamphetamine activation of the subthalamic nucleus and accumbens core and stimulates oxytocinergic neurons in the hypothalamus. Addict Biol. 2010;15(4):448–63.CrossRefPubMed
92.
Zurück zum Zitat Pedersen CA, Smedley KL, Leserman J, Jarskog LF, Rau SW, Kampov-Polevoi A, et al. Intranasal oxytocin blocks alcohol withdrawal in human subjects. Alcohol Clin Exp Res. 2013;37(3):484–9.CrossRefPubMed Pedersen CA, Smedley KL, Leserman J, Jarskog LF, Rau SW, Kampov-Polevoi A, et al. Intranasal oxytocin blocks alcohol withdrawal in human subjects. Alcohol Clin Exp Res. 2013;37(3):484–9.CrossRefPubMed
93.
Zurück zum Zitat Peters S, Slattery DA, Flor PJ, Neumann ID, Reber SO. Differential effects of baclofen and oxytocin on the increased ethanol consumption following chronic psychosocial stress in mice. Addict Biol. 2013;18(1):66–77.CrossRefPubMed Peters S, Slattery DA, Flor PJ, Neumann ID, Reber SO. Differential effects of baclofen and oxytocin on the increased ethanol consumption following chronic psychosocial stress in mice. Addict Biol. 2013;18(1):66–77.CrossRefPubMed
94.
Zurück zum Zitat King CE, Griffin WC, Luderman LN, Kates MM, McGinty JF, Becker HC. Oxytocin reduces ethanol self-administration in mice. Alcohol Clin Exp Res. 2017;41(5):955–64.CrossRefPubMedPubMedCentral King CE, Griffin WC, Luderman LN, Kates MM, McGinty JF, Becker HC. Oxytocin reduces ethanol self-administration in mice. Alcohol Clin Exp Res. 2017;41(5):955–64.CrossRefPubMedPubMedCentral
95.
Zurück zum Zitat King CE, McGinty JF, Becker HC. Effects of oxytocin on stress-induced reinstatement of alcohol-seeking in mice with and without a history of stress. Alcohol. 2017;60:231–2.CrossRef King CE, McGinty JF, Becker HC. Effects of oxytocin on stress-induced reinstatement of alcohol-seeking in mice with and without a history of stress. Alcohol. 2017;60:231–2.CrossRef
96.
Zurück zum Zitat Flanagan JC, Hand A, Jarnecke AM, Moran-Santa Maria MM, Brady KT, Joseph J. Effects of oxytocin on working memory and executive control system connectivity in posttraumatic stress disorder. Exp Clin Psychopharmacol. 2018;26(4):391–402.CrossRefPubMedPubMedCentral Flanagan JC, Hand A, Jarnecke AM, Moran-Santa Maria MM, Brady KT, Joseph J. Effects of oxytocin on working memory and executive control system connectivity in posttraumatic stress disorder. Exp Clin Psychopharmacol. 2018;26(4):391–402.CrossRefPubMedPubMedCentral
97.
Zurück zum Zitat Sippel LM, Allington CE, Pietrzak RH, Harpaz-Rotem I, Mayes LC, Olff M. Oxytocin and stress-related disorders: neurobiological mechanisms and treatment opportunities. Chronic Stress. 2017;1:1–15.CrossRef Sippel LM, Allington CE, Pietrzak RH, Harpaz-Rotem I, Mayes LC, Olff M. Oxytocin and stress-related disorders: neurobiological mechanisms and treatment opportunities. Chronic Stress. 2017;1:1–15.CrossRef
98.
Zurück zum Zitat • Leppanen J, Ng KW, Kim Y, Tchanturia K, Treasure J. Meta-analytic review of the effects of a single dose of intranasal oxytocin on threat processing in humans. J Affect Disord. 2018;225:167–79 Good review of methodological limitations of oxytocin literature.CrossRefPubMed • Leppanen J, Ng KW, Kim Y, Tchanturia K, Treasure J. Meta-analytic review of the effects of a single dose of intranasal oxytocin on threat processing in humans. J Affect Disord. 2018;225:167–79 Good review of methodological limitations of oxytocin literature.CrossRefPubMed
99.
Zurück zum Zitat Walum H, Waldman ID, Young LJ. Statistical and methodological considerations for the interpretation of intranasal oxytocin studies. Biol Psychiatry. 2016;79(3):251–7.CrossRefPubMed Walum H, Waldman ID, Young LJ. Statistical and methodological considerations for the interpretation of intranasal oxytocin studies. Biol Psychiatry. 2016;79(3):251–7.CrossRefPubMed
100.
Zurück zum Zitat Leng G, Ludwig M. Intranasal oxytocin: myths and delusions. Biol Psychiatry. 2016;79(3):243–50.CrossRefPubMed Leng G, Ludwig M. Intranasal oxytocin: myths and delusions. Biol Psychiatry. 2016;79(3):243–50.CrossRefPubMed
101.
Zurück zum Zitat • Kendrick KM, Guastella AJ, Becker B. Overview of human oxytocin research. Curr Top Behav Neurosci. 2017. Comprehensive review of clinical oxytocin literature in psychiatry. • Kendrick KM, Guastella AJ, Becker B. Overview of human oxytocin research. Curr Top Behav Neurosci. 2017. Comprehensive review of clinical oxytocin literature in psychiatry.
102.
Zurück zum Zitat Churchland PS, Winkielman P. Modulating social behavior with oxytocin: how does it work? What does it mean? Horm Behav. 2012;61:392–9.CrossRefPubMed Churchland PS, Winkielman P. Modulating social behavior with oxytocin: how does it work? What does it mean? Horm Behav. 2012;61:392–9.CrossRefPubMed
103.
Zurück zum Zitat Striepens N, Kendrick KM, Hanking V, Landgraf R, Wüllner U, Maier W, et al. Elevated cerebrospinal fluid and blood concentrations of oxytocin following its intranasal administration in humans. Sci Rep. 2013;3:3440.CrossRefPubMedPubMedCentral Striepens N, Kendrick KM, Hanking V, Landgraf R, Wüllner U, Maier W, et al. Elevated cerebrospinal fluid and blood concentrations of oxytocin following its intranasal administration in humans. Sci Rep. 2013;3:3440.CrossRefPubMedPubMedCentral
104.
Zurück zum Zitat Quintana DS, Guastella AJ, Westlye LT, Andreassen OA. The promise and pitfalls of intranasally administering psychopharmacological agents for the treatment of psychiatric disorders. Mol Psychiatry. 2016;21(1):29.CrossRefPubMed Quintana DS, Guastella AJ, Westlye LT, Andreassen OA. The promise and pitfalls of intranasally administering psychopharmacological agents for the treatment of psychiatric disorders. Mol Psychiatry. 2016;21(1):29.CrossRefPubMed
Metadaten
Titel
Augmenting Treatment for Posttraumatic Stress Disorder and Co-Occurring Conditions with Oxytocin
verfasst von
Julianne C. Flanagan, PhD
Jennifer M. Mitchell, PhD
Publikationsdatum
01.06.2019
Verlag
Springer International Publishing
Erschienen in
Current Treatment Options in Psychiatry / Ausgabe 2/2019
Elektronische ISSN: 2196-3061
DOI
https://doi.org/10.1007/s40501-019-00171-1

Weitere Artikel der Ausgabe 2/2019

Current State of the Problem: Opioid Overdose Rates and Deaths

  • Substance Use Disorders (FG Moeller, Section Editor)

New-generation Antipsychotics and Cardiovascular Risk

  • Schizophrenia and Other Psychotic Disorders (J Csernansky, Section Editor)

Brief Novel Therapies for PTSD: Written Exposure Therapy

  • PTSD (S Creech and L Sippel, Section Editors)

Augmenting the Treatment of PTSD with Ketamine—a Review

  • PTSD (S Creech and L Sippel, Section Editors)

Neu im Fachgebiet Psychiatrie

„Wir wollen die Bedeutung von Gen- und Umwelteinflüssen besser verstehen“

Eine Mutation in einem einzelnen Gen kann bei Mäusen eine Art Bipolarstörung auslösen. PD Dr. Jan Deussing vom Max-Planck-Institut für Psychiatrie in München sieht in solchen Tiermodellen eine Möglichkeit, den Ursachen der Erkrankung auf den Grund zu gehen.

Suizidassistenz erhöht Suizidzahlen: Aktuelle Ergebnisse der geplanten S3-Leitlinie

Erstmals wird in Deutschland eine S3-Leitlinie zum Thema Suizidalität erarbeitet. Ziel ist es, die Versorgung in suizidalen Krisen durch einheitliche Standards zu verbessern. Erste Ergebnisse der bisherigen Leitlinienarbeit wurden auf dem DGPPN-Kongress vorgestellt.

Einer von sieben Frauen macht die Menopause sehr zu schaffen

Von mäßigen bis schweren vasomotorischen Beschwerden sind 14,7% der Frauen in der Postmenopause betroffen. Das haben kanadische Forscherinnen in einer Subgruppenanalyse der WARM-Studie herausgefunden.

Depressive Senioren fahren besonders riskant

Beim Autofahren machen ältere Depressive häufiger eine Vollbremsung, gehen öfter zu schnell in Kurven und halten sich seltener an Tempolimits als Senioren ohne Depression. Offenbar scheint eine Depression eine riskante Fahrweise im Alter zu verstärken.

Update Psychiatrie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.