TY - JOUR
T1 - Increased cardiometabolic dysfunction in first-degree relatives of patients with psychotic disorders
AU - Mothi, Suraj Sarvode
AU - Tandon, Neeraj
AU - Padmanabhan, Jaya
AU - Mathew, Ian T.
AU - Clementz, Brett
AU - Tamminga, Carol
AU - Pearlson, Godfrey
AU - Sweeney, John
AU - Keshavan, Matcheri S.
N1 - Funding Information:
This work was supported in part by the National Institute for Mental Health (NIMH) grants MH078113 , MH077945 , MH077852 , MH077851 , MH077862 , MH072767 , and MH083888 .
Funding Information:
GP has served on an advisory panel for Bristol-Myers Squibb. JS has been on advisory boards for Bristol-Myers Squibb, Eli Lilly, Pfizer, Roche, and Takeda and has received grant support from Janssen. CT has the following disclosures to make: Intracellular Therapies (ITI, Inc.)—Advisory Board, drug development; PureTech Ventures—Ad Hoc Consultant; Eli Lilly Pharmaceuticals—Ad Hoc Consultant; Sunovion—Ad Hoc Consultant; Astellas—Ad Hoc Consultant; Cypress Bioscience—Ad Hoc Consultant; Merck—Ad Hoc Consultant; International Congress on Schizophrenia Research—Organizer, unpaid volunteer; National Alliance on Mental Illness—Council Member, unpaid volunteer; American Psychiatric Association—Deputy Editor. MSK has received research support from Sunovion and GlaxoSmithKline. Other authors report no disclosures.
PY - 2015/6/1
Y1 - 2015/6/1
N2 - Introduction: Elevated prevalence of comorbid cardio-vascular and metabolic dysfunction (CMD) is consistently reported in patients with severe psychotic disorders such as schizophrenia (SZ), schizoaffective (SZA) and bipolar disorder (BP-P). Since both psychosis and CMD are substantively heritable in nature, we attempted to investigate the occurrence of CMD disorders in first-degree relatives of probands with psychosis. Methods: Our sample included 861 probands with a diagnosis of SZ (n = 354), SZA (n = 212) and BP-P (n = 295), 776 first-degree relatives of probands and 416 healthy controls. Logistic regression was used to compare prevalence of any CMD disorders (diabetes, hypertension, hyperlipidemia or coronary artery disease) across groups. Post hoc tests of independence checked for CMD prevalence across psychosis diagnosis (SZ, SZA and BP-P), both in relatives of probands and within probands themselves. Results: After controlling for potential confounders, first-degree relatives with (p < 0.001) and without (p = 0.03) Axis I non-psychotic or Axis- II cluster disorders were at a significant risk for CMD compared to controls. No significant difference (p = 0.42) was observed in prevalence of CMD between relatives of SZ, SZA and BP-P, or between psychosis diagnoses for probands (p = 0.25). Discussion: Prevalence of CMD was increased in the first-degree relatives of psychosis subjects. This finding suggests the possibility of overlapping genetic contributions to CMD and psychosis. Increased somatic disease burden in relatives of psychotic disorder probands points to need for early detection and preventive efforts in this population.
AB - Introduction: Elevated prevalence of comorbid cardio-vascular and metabolic dysfunction (CMD) is consistently reported in patients with severe psychotic disorders such as schizophrenia (SZ), schizoaffective (SZA) and bipolar disorder (BP-P). Since both psychosis and CMD are substantively heritable in nature, we attempted to investigate the occurrence of CMD disorders in first-degree relatives of probands with psychosis. Methods: Our sample included 861 probands with a diagnosis of SZ (n = 354), SZA (n = 212) and BP-P (n = 295), 776 first-degree relatives of probands and 416 healthy controls. Logistic regression was used to compare prevalence of any CMD disorders (diabetes, hypertension, hyperlipidemia or coronary artery disease) across groups. Post hoc tests of independence checked for CMD prevalence across psychosis diagnosis (SZ, SZA and BP-P), both in relatives of probands and within probands themselves. Results: After controlling for potential confounders, first-degree relatives with (p < 0.001) and without (p = 0.03) Axis I non-psychotic or Axis- II cluster disorders were at a significant risk for CMD compared to controls. No significant difference (p = 0.42) was observed in prevalence of CMD between relatives of SZ, SZA and BP-P, or between psychosis diagnoses for probands (p = 0.25). Discussion: Prevalence of CMD was increased in the first-degree relatives of psychosis subjects. This finding suggests the possibility of overlapping genetic contributions to CMD and psychosis. Increased somatic disease burden in relatives of psychotic disorder probands points to need for early detection and preventive efforts in this population.
KW - Diabetes
KW - Hypertension
KW - Psychotic disorder
KW - Relatives
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U2 - 10.1016/j.schres.2015.03.034
DO - 10.1016/j.schres.2015.03.034
M3 - Article
C2 - 25900543
AN - SCOPUS:84929510158
VL - 165
SP - 103
EP - 107
JO - Schizophrenia Research
JF - Schizophrenia Research
SN - 0920-9964
IS - 1
ER -