Genetic susceptibility to multiple sclerosis: Brain structure and cognitive function in the general population

被引:8
|
作者
Ikram, Mohammad Arfan [1 ,2 ,3 ]
Vernooij, Meike W. [1 ,2 ]
Roshchupkin, Gennady V. [2 ,4 ]
Hofman, Albert [1 ,5 ]
van Duijn, Cornelia M. [1 ]
Uitterlinden, Andre G. [4 ]
Niessen, Wiro J. [2 ,3 ,6 ]
Hintzen, Rogier Q. [3 ]
Adams, Hieab H. H. [1 ,2 ]
机构
[1] Erasmus Univ, Med Ctr Erasmus MC, Dept Epidemiol, Wytemaweg 80, NL-3015 CE Rotterdam, Netherlands
[2] Erasmus Univ, Med Ctr Erasmus MC, Dept Radiol, Rotterdam, Netherlands
[3] Erasmus Univ, Med Ctr Erasmus MC, Dept Neurol, Rotterdam, Netherlands
[4] Erasmus Univ, Med Ctr Erasmus MC, Dept Med Informat, Rotterdam, Netherlands
[5] Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA USA
[6] Delft Univ Technol, Fac Appl Sci, Delft, Netherlands
关键词
Epidemiology; multiple sclerosis; magnetic resonance imaging; genetics; APPEARING WHITE-MATTER; TISSUE SEGMENTATION; RISK; IMPAIRMENT; METAANALYSIS; ASSOCIATION; DYSFUNCTION; ROTTERDAM; LESIONS; ATROPHY;
D O I
10.1177/1352458516682104
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Multiple sclerosis (MS) affects brain structure and cognitive function and has a heritable component. Over a 100 common genetic risk variants have been identified, but most carriers do not develop MS. For other neurodegenerative diseases, risk variants have effects outside patient populations, but this remains uninvestigated for MS. Objectives: To study the effect of MS-associated genetic variants on brain structure and cognitive function in the general population. Methods: We studied middle-aged and elderly individuals (mean age = 65.7 years) from the population-based Rotterdam Study. We determined 107 MS variants and additionally created a risk score combining all variants. Magnetic resonance imaging (N = 4710) was performed to obtain measures of brain macrostructure, white matter microstructure, and gray matter voxel-based morphometry. A cognitive test battery (N = 7556) was used to test a variety of cognitive domains. Results: The MS risk score was associated with smaller gray matter volume over the whole brain (beta(standardized) = -0.016; p = 0.044), but region-specific analyses did not survive multiple testing correction. Similarly, no significant associations with brain structure were observed for individual variants. For cognition, rs2283792 was significantly associated with poorer memory (beta = -0.064; p = 3.4 x 10(-5)). Conclusion: Increased genetic susceptibility to MS may affect brain structure and cognition in persons without disease, pointing to a "hidden burden" of MS.
引用
收藏
页码:1697 / 1706
页数:10
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