High-sensitive C-reactive protein and homocysteine levels in patients with newly diagnosed bipolar disorder, their first-degree relatives, and healthy control persons-Results from a clinical study
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High-sensitive C-reactive protein and homocysteine levels in patients with newly diagnosed bipolar disorder, their first-degree relatives, and healthy control persons-Results from a clinical study. / Nielsen, Marc Østergaard; Petersen, Nanna Aagaard; Coello, Klara; Stanislaus, Sharleny; Melbye, Sigurd A.; Kjærstad, Hanne Lie; Sletved, Kimie Stefanie Ormstrup; Frikke-Schmidt, Ruth; McIntyre, Roger S.; Vinberg, Maj; Kessing, Lars Vedel.
I: European psychiatry : the journal of the Association of European Psychiatrists, Bind 63, Nr. 1, 2020, s. e103.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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T1 - High-sensitive C-reactive protein and homocysteine levels in patients with newly diagnosed bipolar disorder, their first-degree relatives, and healthy control persons-Results from a clinical study
AU - Nielsen, Marc Østergaard
AU - Petersen, Nanna Aagaard
AU - Coello, Klara
AU - Stanislaus, Sharleny
AU - Melbye, Sigurd A.
AU - Kjærstad, Hanne Lie
AU - Sletved, Kimie Stefanie Ormstrup
AU - Frikke-Schmidt, Ruth
AU - McIntyre, Roger S.
AU - Vinberg, Maj
AU - Kessing, Lars Vedel
PY - 2020
Y1 - 2020
N2 - BACKGROUND: Changes in inflammatory and metabolic markers are implicated in the pathogenesis in both the development and progression of bipolar disorder (BD). Notwithstanding, these markers have not been investigated in newly diagnosed BD. METHODS: We compared high-sensitive C-reactive protein (hs-CRP) and homocysteine (Hcy) levels in 372 patients with newly diagnosed BD, 106 unaffected first-degree relatives (URs), and 201 healthy control persons (HCs). Within the patient group, we also investigated possible associations between hs-CRP and Hcy, respectively, with illness-related characteristics and psychotropic medication. RESULTS: No statistically significant differences in Hcy and hs-CRP levels were found when comparing BD and URs with HCs. Similarly, there were no differences when comparing only patients in remission or patients with affective symptoms, respectively, with HCs. Hcy levels were found to be 11.9% (95% CI: 1.030-1.219) higher in patients with BD when compared with their URs (p = 0.008), when adjusting for folate and cobalamin status, age, sex, and self-reported activity levels. Hcy levels were significantly associated with folate, cobalamin, gender, and age in all models (p < 0.05). CONCLUSION: Our results do not support hs-CRP or Hcy as markers in newly diagnosed BD.
AB - BACKGROUND: Changes in inflammatory and metabolic markers are implicated in the pathogenesis in both the development and progression of bipolar disorder (BD). Notwithstanding, these markers have not been investigated in newly diagnosed BD. METHODS: We compared high-sensitive C-reactive protein (hs-CRP) and homocysteine (Hcy) levels in 372 patients with newly diagnosed BD, 106 unaffected first-degree relatives (URs), and 201 healthy control persons (HCs). Within the patient group, we also investigated possible associations between hs-CRP and Hcy, respectively, with illness-related characteristics and psychotropic medication. RESULTS: No statistically significant differences in Hcy and hs-CRP levels were found when comparing BD and URs with HCs. Similarly, there were no differences when comparing only patients in remission or patients with affective symptoms, respectively, with HCs. Hcy levels were found to be 11.9% (95% CI: 1.030-1.219) higher in patients with BD when compared with their URs (p = 0.008), when adjusting for folate and cobalamin status, age, sex, and self-reported activity levels. Hcy levels were significantly associated with folate, cobalamin, gender, and age in all models (p < 0.05). CONCLUSION: Our results do not support hs-CRP or Hcy as markers in newly diagnosed BD.
KW - Bipolar disorder
KW - C-reactive protein
KW - homocysteine
KW - unaffected relatives
U2 - 10.1192/j.eurpsy.2020.105
DO - 10.1192/j.eurpsy.2020.105
M3 - Journal article
C2 - 33234170
AN - SCOPUS:85098531686
VL - 63
SP - e103
JO - European Psychiatry
JF - European Psychiatry
SN - 0924-9338
IS - 1
ER -
ID: 255211281