Bipolar spectrum disorders are associated with increased gray matter volume in the medial orbitofrontal cortex and nucleus accumbens.
Bipolar spectrum disorders are associated with increased gray matter volume in the medial orbitofrontal cortex and nucleus accumbens.
复制标题
双相谱系障碍与内侧眶额皮质和伏核灰质体积增加有关。
DOI:
10.1002/jcv2.12068
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发表时间:
2022
期刊:
影响因子:
--
通讯作者:
Nusslock,Robin
中科院分区:
文献类型:
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作者:
Damme,KatherineSF;Alloy,LaurenB;Kelley,NicholasJ;Carroll,Ann;Young,ChristinaB;Chein,Jason;Ng,TommyH;Titone,MadisonK;Bart,CorinneP;Nusslock,Robin
ObjectiveElevated sensitivity to rewards prospectively predicts Bipolar Spectrum Disorder (BSD) onset; however, it is unclear whether volumetric abnormalities also reflect BSD risk. BSDs emerge when critical neurodevelopment in frontal and striatal regions occurs in sex‐specific ways. The current paper examined the volume of frontal and striatal brain regions in both individuals with and at risk for a BSD with exploratory analyses examining sex‐specificity.MethodsOne hundred fourteen medication‐free individuals ages 18–27 at low‐risk for BSD (moderate‐reward sensitivity;N= 37), at high‐risk without a BSD (high‐reward sensitivity;N= 47), or with a BSD (N= 30) completed a structural MRI scan of the brain. We examined group differences in gray matter volume in a priori medial orbitofrontal cortex (mOFC) and nucleus accumbens (NAcc) regions‐of‐interest.ResultsThe BSD group had enlarged frontostriatal volumes (mOFC, NAcc) compared to low individuals (d= 1.01). The mOFC volume in BSD was larger than low‐risk (d= 1.01) and the high‐risk groups (d= 0.74). This effect was driven by males with a BSD, who showed an enlarged mOFC compared to low (d= 1.01) and high‐risk males (d= 0.74). Males with a BSD also showed a greater NAcc volume compared to males at low‐risk (d= 0.49), but not high‐risk males.ConclusionsAn enlarged frontostriatal volume (averaged mOFC, NAcc) is associated with the presence of a BSD, while subvolumes (mOFC vs. NAcc) showed unique patterning in relation to risk. We report preliminary evidence that sex moderates frontostriatal volume in BSD, highlighting the need for larger longitudinal risk studies examining the role of sex‐specific neurodevelopmental trajectories in emerging BSDs.