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Visceral obesity relates to deep white matter hyperintensities via inflammation

Objective White matter hyperintensities (WMHs) are linked to vascular risk factors and increase the risk of cognitive decline, dementia, and stroke. We here aimed to determine whether obesity contributes to regional WMHs using a whole‐brain approach in a well‐characterized population‐based cohort. M...

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Published in:Annals of neurology 2019-02, Vol.85 (2), p.194-203
Main Authors: Lampe, Leonie, Zhang, Rui, Beyer, Frauke, Huhn, Sebastian, Kharabian Masouleh, Shahrzad, Preusser, Sven, Bazin, Pierre‐Louis, Schroeter, Matthias L., Villringer, Arno, Witte, A. Veronica
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container_title Annals of neurology
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creator Lampe, Leonie
Zhang, Rui
Beyer, Frauke
Huhn, Sebastian
Kharabian Masouleh, Shahrzad
Preusser, Sven
Bazin, Pierre‐Louis
Schroeter, Matthias L.
Villringer, Arno
Witte, A. Veronica
description Objective White matter hyperintensities (WMHs) are linked to vascular risk factors and increase the risk of cognitive decline, dementia, and stroke. We here aimed to determine whether obesity contributes to regional WMHs using a whole‐brain approach in a well‐characterized population‐based cohort. Methods Waist‐to‐hip ratio (WHR), body mass index (BMI), systolic/diastolic blood pressure, hypertension, diabetes and smoking status, blood glucose and inflammatory markers, as well as distribution of WMH were assessed in 1,825 participants of the LIFE‐adult study (age, 20–82 years; BMI, 18.4–55.4 kg/m2) using high‐resolution 3‐Tesla magnetic resonance imaging. Voxel‐wise analyses tested if obesity predicts regional probability of WMH. Additionally, mediation effects of high‐sensitive C‐reactive protein and interleukin‐6 (IL6) measured in blood were related to obesity and WMH using linear regression and structural equation models. Results WHR related to higher WMH probability predominantly in the deep white matter, even after adjusting for effects of age, sex, and systolic blood pressure (mean ß = 0.0043 [0.0008 SE], 95% confidence interval, [0.00427, 0.0043]; threshold‐free cluster enhancement, family‐wise error‐corrected p < 0.05). Conversely, higher systolic blood pressure was associated with WMH in periventricular white matter regions. Mediation analyses indicated that both higher WHR and higher BMI contributed to increased deep‐to‐periventricular WMH ratio through elevated IL6. Interpretation Our results indicate an increased WMH burden selectively in the deep white matter in obese subjects with high visceral fat accumulation, independent of common obesity comorbidities such as hypertension. Mediation analyses proposed that visceral obesity contributes to deep white matter lesions through increases in proinflammatory cytokines, suggesting a pathomechanistic link. Longitudinal studies need to confirm this hypothesis. ANN NEUROL 2019;85:194–203.
doi_str_mv 10.1002/ana.25396
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Veronica</creator><creatorcontrib>Lampe, Leonie ; Zhang, Rui ; Beyer, Frauke ; Huhn, Sebastian ; Kharabian Masouleh, Shahrzad ; Preusser, Sven ; Bazin, Pierre‐Louis ; Schroeter, Matthias L. ; Villringer, Arno ; Witte, A. Veronica</creatorcontrib><description>Objective White matter hyperintensities (WMHs) are linked to vascular risk factors and increase the risk of cognitive decline, dementia, and stroke. We here aimed to determine whether obesity contributes to regional WMHs using a whole‐brain approach in a well‐characterized population‐based cohort. Methods Waist‐to‐hip ratio (WHR), body mass index (BMI), systolic/diastolic blood pressure, hypertension, diabetes and smoking status, blood glucose and inflammatory markers, as well as distribution of WMH were assessed in 1,825 participants of the LIFE‐adult study (age, 20–82 years; BMI, 18.4–55.4 kg/m2) using high‐resolution 3‐Tesla magnetic resonance imaging. Voxel‐wise analyses tested if obesity predicts regional probability of WMH. Additionally, mediation effects of high‐sensitive C‐reactive protein and interleukin‐6 (IL6) measured in blood were related to obesity and WMH using linear regression and structural equation models. Results WHR related to higher WMH probability predominantly in the deep white matter, even after adjusting for effects of age, sex, and systolic blood pressure (mean ß = 0.0043 [0.0008 SE], 95% confidence interval, [0.00427, 0.0043]; threshold‐free cluster enhancement, family‐wise error‐corrected p &lt; 0.05). Conversely, higher systolic blood pressure was associated with WMH in periventricular white matter regions. Mediation analyses indicated that both higher WHR and higher BMI contributed to increased deep‐to‐periventricular WMH ratio through elevated IL6. Interpretation Our results indicate an increased WMH burden selectively in the deep white matter in obese subjects with high visceral fat accumulation, independent of common obesity comorbidities such as hypertension. Mediation analyses proposed that visceral obesity contributes to deep white matter lesions through increases in proinflammatory cytokines, suggesting a pathomechanistic link. Longitudinal studies need to confirm this hypothesis. 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Annals of Neurology published by Wiley Periodicals, Inc. on behalf of American Neurological Association.</rights><rights>2019 American Neurological Association</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4436-e8b9d4d22164733634606f7ffb69d87cca47f880c9459fbecfc38d1f3b76805c3</citedby><cites>FETCH-LOGICAL-c4436-e8b9d4d22164733634606f7ffb69d87cca47f880c9459fbecfc38d1f3b76805c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30556596$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lampe, Leonie</creatorcontrib><creatorcontrib>Zhang, Rui</creatorcontrib><creatorcontrib>Beyer, Frauke</creatorcontrib><creatorcontrib>Huhn, Sebastian</creatorcontrib><creatorcontrib>Kharabian Masouleh, Shahrzad</creatorcontrib><creatorcontrib>Preusser, Sven</creatorcontrib><creatorcontrib>Bazin, Pierre‐Louis</creatorcontrib><creatorcontrib>Schroeter, Matthias L.</creatorcontrib><creatorcontrib>Villringer, Arno</creatorcontrib><creatorcontrib>Witte, A. Veronica</creatorcontrib><title>Visceral obesity relates to deep white matter hyperintensities via inflammation</title><title>Annals of neurology</title><addtitle>Ann Neurol</addtitle><description>Objective White matter hyperintensities (WMHs) are linked to vascular risk factors and increase the risk of cognitive decline, dementia, and stroke. We here aimed to determine whether obesity contributes to regional WMHs using a whole‐brain approach in a well‐characterized population‐based cohort. Methods Waist‐to‐hip ratio (WHR), body mass index (BMI), systolic/diastolic blood pressure, hypertension, diabetes and smoking status, blood glucose and inflammatory markers, as well as distribution of WMH were assessed in 1,825 participants of the LIFE‐adult study (age, 20–82 years; BMI, 18.4–55.4 kg/m2) using high‐resolution 3‐Tesla magnetic resonance imaging. Voxel‐wise analyses tested if obesity predicts regional probability of WMH. Additionally, mediation effects of high‐sensitive C‐reactive protein and interleukin‐6 (IL6) measured in blood were related to obesity and WMH using linear regression and structural equation models. Results WHR related to higher WMH probability predominantly in the deep white matter, even after adjusting for effects of age, sex, and systolic blood pressure (mean ß = 0.0043 [0.0008 SE], 95% confidence interval, [0.00427, 0.0043]; threshold‐free cluster enhancement, family‐wise error‐corrected p &lt; 0.05). Conversely, higher systolic blood pressure was associated with WMH in periventricular white matter regions. Mediation analyses indicated that both higher WHR and higher BMI contributed to increased deep‐to‐periventricular WMH ratio through elevated IL6. Interpretation Our results indicate an increased WMH burden selectively in the deep white matter in obese subjects with high visceral fat accumulation, independent of common obesity comorbidities such as hypertension. Mediation analyses proposed that visceral obesity contributes to deep white matter lesions through increases in proinflammatory cytokines, suggesting a pathomechanistic link. Longitudinal studies need to confirm this hypothesis. 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Veronica</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Visceral obesity relates to deep white matter hyperintensities via inflammation</atitle><jtitle>Annals of neurology</jtitle><addtitle>Ann Neurol</addtitle><date>2019-02</date><risdate>2019</risdate><volume>85</volume><issue>2</issue><spage>194</spage><epage>203</epage><pages>194-203</pages><issn>0364-5134</issn><eissn>1531-8249</eissn><abstract>Objective White matter hyperintensities (WMHs) are linked to vascular risk factors and increase the risk of cognitive decline, dementia, and stroke. We here aimed to determine whether obesity contributes to regional WMHs using a whole‐brain approach in a well‐characterized population‐based cohort. Methods Waist‐to‐hip ratio (WHR), body mass index (BMI), systolic/diastolic blood pressure, hypertension, diabetes and smoking status, blood glucose and inflammatory markers, as well as distribution of WMH were assessed in 1,825 participants of the LIFE‐adult study (age, 20–82 years; BMI, 18.4–55.4 kg/m2) using high‐resolution 3‐Tesla magnetic resonance imaging. Voxel‐wise analyses tested if obesity predicts regional probability of WMH. Additionally, mediation effects of high‐sensitive C‐reactive protein and interleukin‐6 (IL6) measured in blood were related to obesity and WMH using linear regression and structural equation models. Results WHR related to higher WMH probability predominantly in the deep white matter, even after adjusting for effects of age, sex, and systolic blood pressure (mean ß = 0.0043 [0.0008 SE], 95% confidence interval, [0.00427, 0.0043]; threshold‐free cluster enhancement, family‐wise error‐corrected p &lt; 0.05). Conversely, higher systolic blood pressure was associated with WMH in periventricular white matter regions. Mediation analyses indicated that both higher WHR and higher BMI contributed to increased deep‐to‐periventricular WMH ratio through elevated IL6. Interpretation Our results indicate an increased WMH burden selectively in the deep white matter in obese subjects with high visceral fat accumulation, independent of common obesity comorbidities such as hypertension. Mediation analyses proposed that visceral obesity contributes to deep white matter lesions through increases in proinflammatory cytokines, suggesting a pathomechanistic link. Longitudinal studies need to confirm this hypothesis. ANN NEUROL 2019;85:194–203.</abstract><cop>Hoboken, USA</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>30556596</pmid><doi>10.1002/ana.25396</doi><tpages>203</tpages><oa>free_for_read</oa></addata></record>
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ispartof Annals of neurology, 2019-02, Vol.85 (2), p.194-203
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1531-8249
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source Wiley
subjects Adult
Age factors
Aged
Aged, 80 and over
Blood pressure
Body mass
Body Mass Index
Body size
Brain
Cognitive ability
Cohort Studies
Confidence intervals
Correlation analysis
Cytokines
Dementia disorders
Diabetes mellitus
Error correction
Female
Hip
Humans
Hypertension
Inflammation
Inflammation - blood
Inflammation - diagnostic imaging
Inflammation Mediators - blood
Interleukin 6
Lesions
Longitudinal studies
Magnetic resonance imaging
Male
Mediation
Middle Aged
Neuroimaging
Obesity
Obesity, Abdominal - blood
Obesity, Abdominal - diagnostic imaging
Proteins
Regional analysis
Regression analysis
Risk analysis
Risk factors
Smoking
Statistical analysis
Substantia alba
Waist-Hip Ratio
White Matter - diagnostic imaging
Young Adult
title Visceral obesity relates to deep white matter hyperintensities via inflammation
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