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Sökning: onr:"swepub:oai:lup.lub.lu.se:98f85b1e-8960-493e-840c-c02a86f2eced" > Biological predicto...

Biological predictors of insulin resistance associated with posttraumatic stress disorder in young military veterans

Blessing, Esther M. (författare)
New York University
Reus, Victor I (författare)
University of California, San Francisco
Mellon, Synthia H (författare)
University of California, San Francisco
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Wolkowitz, Owen M (författare)
University of California, San Francisco
Flory, Janine D (författare)
Icahn School of Medicine at Mount Sinai
Bierer, Linda M (författare)
Icahn School of Medicine at Mount Sinai
Lindqvist, Daniel (författare)
Lund University,Lunds universitet,Psykiatri, Lund,Sektion IV,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Psychiatry (Lund),Section IV,Department of Clinical Sciences, Lund,Faculty of Medicine,University of California, San Francisco
Dhabhar, Firdaus S (författare)
University of Miami
Li, Meng (författare)
New York University
Qian, Meng (författare)
New York University
Abu-Amara, Duna (författare)
New York University
Galatzer-Levy, Isaac (författare)
New York University
Yehuda, Rachel (författare)
Icahn School of Medicine at Mount Sinai
Marmar, Charles R (författare)
New York University
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 (creator_code:org_t)
Elsevier BV, 2017
2017
Engelska.
Ingår i: Psychoneuroendocrinology. - : Elsevier BV. - 0306-4530. ; 82, s. 91-97
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Posttraumatic stress disorder (PTSD) is associated with increased risk for Type 2 diabetes and cardiovascular disease (cardiometabolic disease), warranting research into targeted prevention strategies. In the present case–control study of 160 young (mean age 32.7 years) male military veterans, we aimed to assess whether PTSD status predicted increased markers of cardiometabolic risk in otherwise healthy individuals, and further, to explore biological pathways between PTSD and these increased markers of cardiometabolic risk. Toward these aims, we compared measures of cardiometabolic risk, namely insulin resistance (IR) (HOMA-IR), metabolic syndrome (MetS) and prediabetes, between 80 PTSD cases and 80 controls without PTSD. We then determined whether PTSD-associated increases in HOMA-IR were correlated with select biological variables from pathways previously hypothesized to link PTSD with cardiometabolic risk, including systemic inflammation (increased C-reactive protein, interleukin-6, and tumor necrosis factor α), sympathetic over-activity (increased resting heart rate), and neuroendocrine dysregulation (increased plasma cortisol or serum brain-derived neurotrophic factor (BDNF)). We found PTSD diagnosis was associated with substantially higher HOMA-IR (cases 4.3 ± 4.3 vs controls 2.4 ± 2.0; p < 0.001), and a higher frequency of MetS (cases 21.3% vs controls 2.5%; p < 0.001), but not prediabetes (cases 20.0% vs controls 18.8%; p > 0.05). Cases also had increased pro-inflammatory cytokines (p < 0.01), heart rate (p < 0.001), and BDNF (p < 0.001), which together predicted increased HOMA-IR (adjusted R2 = 0.68, p < 0.001). Results show PTSD diagnosis in young male military veterans without cardiometabolic disease is associated with increased IR, predicted by biological alterations previously hypothesized to link PTSD to increased cardiometabolic risk. Findings support further research into early, targeted prevention of cardiometabolic disease in individuals with PTSD.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Psykiatri (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Psychiatry (hsv//eng)

Nyckelord

Brain derived neurotrophic factor
Inflammation
Insulin resistance
Prediabetes
PTSD
Sympathetic

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