@article{RN349,
   author = {Beran, M. and van Gennip, A. C. E. and Stehouwer, C. D. A. and Jansen, J. F. A. and Gupta, M. D. and Houben, Ajhm and Berendschot, Ttjm and Webers, C. A. B. and Wesselius, A. and Schalkwijk, C. G. and Backes, W. H. and de Jong, J. J. A. and van der Kallen, C. J. H. and van Greevenbroek, M. M. J. and Kohler, S. and Vonk, J. M. J. and Geerlings, M. I. and Schram, M. T. and van Sloten, T. T.},
   title = {Microvascular Dysfunction and Whole-Brain White Matter Connectivity: The Maastricht Study},
   journal = {J Am Heart Assoc},
   pages = {e9112},
   note = {Beran, Magdalena
van Gennip, April C E
Stehouwer, Coen D A
Jansen, Jacobus F A
Gupta, Monideepa D
Houben, Alfons J H M
Berendschot, Tos T J M
Webers, Carroll A B
Wesselius, Anke
Schalkwijk, Casper G
Backes, Walter H
de Jong, Joost J A
van der Kallen, Carla J H
van Greevenbroek, Marleen M J
Kohler, Sebastian
Vonk, Jet M J
Geerlings, Mirjam I
Schram, Miranda T
van Sloten, Thomas T
eng
England
J Am Heart Assoc. 2024 Jan 19:e9112. doi: 10.1161/JAHA.123.031573.},
   abstract = {BACKGROUND: Microvascular dysfunction is involved in the development of various cerebral disorders. It may contribute to these disorders by disrupting white matter tracts and altering brain connectivity, but evidence is scarce. We investigated the association between multiple biomarkers of microvascular function and whole-brain white matter connectivity. METHODS AND RESULTS: Cross-sectional data from The Maastricht Study, a Dutch population-based cohort (n=4326; age, 59.4+/-8.6 years; 49.7% women). Measures of microvascular function included urinary albumin excretion, central retinal arteriolar and venular calibers, composite scores of flicker light-induced retinal arteriolar and venular dilation, and plasma biomarkers of endothelial dysfunction (intercellular adhesion molecule-1, vascular cell adhesion molecule-1, E-selectin, and von Willebrand factor). White matter connectivity was calculated from 3T diffusion magnetic resonance imaging to quantify the number (average node degree) and organization (characteristic path length, global efficiency, clustering coefficient, and local efficiency) of white matter connections. A higher plasma biomarkers of endothelial dysfunction composite score was associated with a longer characteristic path length (beta per SD, 0.066 [95% CI, 0.017-0.114]) after adjustment for sociodemographic, lifestyle, and cardiovascular factors but not with any of the other white matter connectivity measures. After multiple comparison correction, this association was nonsignificant. None of the other microvascular function measures were associated with any of the connectivity measures. CONCLUSIONS: These findings suggest that microvascular dysfunction as measured by indirect markers is not associated with whole-brain white matter connectivity.},
   keywords = {cerebral microcirculation
cohort
diffusion tensor imaging
microvascular dysfunction
white matter connectivity},
   ISSN = {2047-9980 (Electronic)
2047-9980 (Linking)},
   DOI = {10.1161/JAHA.123.031573},
   url = {https://www.ncbi.nlm.nih.gov/pubmed/38240213},
   year = {2024},
   type = {Journal Article}
}

{"_id":"J8prpfoYkytMwSHhH","bibbaseid":"beran-vangennip-stehouwer-jansen-gupta-houben-berendschot-webers-etal-microvasculardysfunctionandwholebrainwhitematterconnectivitythemaastrichtstudy-2024","author_short":["Beran, M.","van Gennip, A. C. E.","Stehouwer, C. D. A.","Jansen, J. F. A.","Gupta, M. D.","Houben, A.","Berendschot, T.","Webers, C. A. B.","Wesselius, A.","Schalkwijk, C. G.","Backes, W. H.","de Jong, J. J. A.","van der Kallen, C. J. H.","van Greevenbroek, M. M. J.","Kohler, S.","Vonk, J. M. J.","Geerlings, M. I.","Schram, M. T.","van Sloten, T. T."],"bibdata":{"bibtype":"article","type":"Journal Article","author":[{"propositions":[],"lastnames":["Beran"],"firstnames":["M."],"suffixes":[]},{"propositions":["van"],"lastnames":["Gennip"],"firstnames":["A.","C.","E."],"suffixes":[]},{"propositions":[],"lastnames":["Stehouwer"],"firstnames":["C.","D.","A."],"suffixes":[]},{"propositions":[],"lastnames":["Jansen"],"firstnames":["J.","F.","A."],"suffixes":[]},{"propositions":[],"lastnames":["Gupta"],"firstnames":["M.","D."],"suffixes":[]},{"propositions":[],"lastnames":["Houben"],"firstnames":["Ajhm"],"suffixes":[]},{"propositions":[],"lastnames":["Berendschot"],"firstnames":["Ttjm"],"suffixes":[]},{"propositions":[],"lastnames":["Webers"],"firstnames":["C.","A.","B."],"suffixes":[]},{"propositions":[],"lastnames":["Wesselius"],"firstnames":["A."],"suffixes":[]},{"propositions":[],"lastnames":["Schalkwijk"],"firstnames":["C.","G."],"suffixes":[]},{"propositions":[],"lastnames":["Backes"],"firstnames":["W.","H."],"suffixes":[]},{"propositions":["de"],"lastnames":["Jong"],"firstnames":["J.","J.","A."],"suffixes":[]},{"propositions":["van","der"],"lastnames":["Kallen"],"firstnames":["C.","J.","H."],"suffixes":[]},{"propositions":["van"],"lastnames":["Greevenbroek"],"firstnames":["M.","M.","J."],"suffixes":[]},{"propositions":[],"lastnames":["Kohler"],"firstnames":["S."],"suffixes":[]},{"propositions":[],"lastnames":["Vonk"],"firstnames":["J.","M.","J."],"suffixes":[]},{"propositions":[],"lastnames":["Geerlings"],"firstnames":["M.","I."],"suffixes":[]},{"propositions":[],"lastnames":["Schram"],"firstnames":["M.","T."],"suffixes":[]},{"propositions":["van"],"lastnames":["Sloten"],"firstnames":["T.","T."],"suffixes":[]}],"title":"Microvascular Dysfunction and Whole-Brain White Matter Connectivity: The Maastricht Study","journal":"J Am Heart Assoc","pages":"e9112","note":"Beran, Magdalena van Gennip, April C E Stehouwer, Coen D A Jansen, Jacobus F A Gupta, Monideepa D Houben, Alfons J H M Berendschot, Tos T J M Webers, Carroll A B Wesselius, Anke Schalkwijk, Casper G Backes, Walter H de Jong, Joost J A van der Kallen, Carla J H van Greevenbroek, Marleen M J Kohler, Sebastian Vonk, Jet M J Geerlings, Mirjam I Schram, Miranda T van Sloten, Thomas T eng England J Am Heart Assoc. 2024 Jan 19:e9112. doi: 10.1161/JAHA.123.031573.","abstract":"BACKGROUND: Microvascular dysfunction is involved in the development of various cerebral disorders. It may contribute to these disorders by disrupting white matter tracts and altering brain connectivity, but evidence is scarce. We investigated the association between multiple biomarkers of microvascular function and whole-brain white matter connectivity. METHODS AND RESULTS: Cross-sectional data from The Maastricht Study, a Dutch population-based cohort (n=4326; age, 59.4+/-8.6 years; 49.7% women). Measures of microvascular function included urinary albumin excretion, central retinal arteriolar and venular calibers, composite scores of flicker light-induced retinal arteriolar and venular dilation, and plasma biomarkers of endothelial dysfunction (intercellular adhesion molecule-1, vascular cell adhesion molecule-1, E-selectin, and von Willebrand factor). White matter connectivity was calculated from 3T diffusion magnetic resonance imaging to quantify the number (average node degree) and organization (characteristic path length, global efficiency, clustering coefficient, and local efficiency) of white matter connections. A higher plasma biomarkers of endothelial dysfunction composite score was associated with a longer characteristic path length (beta per SD, 0.066 [95% CI, 0.017-0.114]) after adjustment for sociodemographic, lifestyle, and cardiovascular factors but not with any of the other white matter connectivity measures. After multiple comparison correction, this association was nonsignificant. None of the other microvascular function measures were associated with any of the connectivity measures. CONCLUSIONS: These findings suggest that microvascular dysfunction as measured by indirect markers is not associated with whole-brain white matter connectivity.","keywords":"cerebral microcirculation cohort diffusion tensor imaging microvascular dysfunction white matter connectivity","issn":"2047-9980 (Electronic) 2047-9980 (Linking)","doi":"10.1161/JAHA.123.031573","url":"https://www.ncbi.nlm.nih.gov/pubmed/38240213","year":"2024","bibtex":"@article{RN349,\n author = {Beran, M. and van Gennip, A. C. E. and Stehouwer, C. D. A. and Jansen, J. F. A. and Gupta, M. D. and Houben, Ajhm and Berendschot, Ttjm and Webers, C. A. B. and Wesselius, A. and Schalkwijk, C. G. and Backes, W. H. and de Jong, J. J. A. and van der Kallen, C. J. H. and van Greevenbroek, M. M. J. and Kohler, S. and Vonk, J. M. J. and Geerlings, M. I. and Schram, M. T. and van Sloten, T. T.},\n title = {Microvascular Dysfunction and Whole-Brain White Matter Connectivity: The Maastricht Study},\n journal = {J Am Heart Assoc},\n pages = {e9112},\n note = {Beran, Magdalena\nvan Gennip, April C E\nStehouwer, Coen D A\nJansen, Jacobus F A\nGupta, Monideepa D\nHouben, Alfons J H M\nBerendschot, Tos T J M\nWebers, Carroll A B\nWesselius, Anke\nSchalkwijk, Casper G\nBackes, Walter H\nde Jong, Joost J A\nvan der Kallen, Carla J H\nvan Greevenbroek, Marleen M J\nKohler, Sebastian\nVonk, Jet M J\nGeerlings, Mirjam I\nSchram, Miranda T\nvan Sloten, Thomas T\neng\nEngland\nJ Am Heart Assoc. 2024 Jan 19:e9112. doi: 10.1161/JAHA.123.031573.},\n abstract = {BACKGROUND: Microvascular dysfunction is involved in the development of various cerebral disorders. It may contribute to these disorders by disrupting white matter tracts and altering brain connectivity, but evidence is scarce. We investigated the association between multiple biomarkers of microvascular function and whole-brain white matter connectivity. METHODS AND RESULTS: Cross-sectional data from The Maastricht Study, a Dutch population-based cohort (n=4326; age, 59.4+/-8.6 years; 49.7% women). Measures of microvascular function included urinary albumin excretion, central retinal arteriolar and venular calibers, composite scores of flicker light-induced retinal arteriolar and venular dilation, and plasma biomarkers of endothelial dysfunction (intercellular adhesion molecule-1, vascular cell adhesion molecule-1, E-selectin, and von Willebrand factor). White matter connectivity was calculated from 3T diffusion magnetic resonance imaging to quantify the number (average node degree) and organization (characteristic path length, global efficiency, clustering coefficient, and local efficiency) of white matter connections. A higher plasma biomarkers of endothelial dysfunction composite score was associated with a longer characteristic path length (beta per SD, 0.066 [95% CI, 0.017-0.114]) after adjustment for sociodemographic, lifestyle, and cardiovascular factors but not with any of the other white matter connectivity measures. After multiple comparison correction, this association was nonsignificant. None of the other microvascular function measures were associated with any of the connectivity measures. CONCLUSIONS: These findings suggest that microvascular dysfunction as measured by indirect markers is not associated with whole-brain white matter connectivity.},\n keywords = {cerebral microcirculation\ncohort\ndiffusion tensor imaging\nmicrovascular dysfunction\nwhite matter connectivity},\n ISSN = {2047-9980 (Electronic)\n2047-9980 (Linking)},\n DOI = {10.1161/JAHA.123.031573},\n url = {https://www.ncbi.nlm.nih.gov/pubmed/38240213},\n year = {2024},\n type = {Journal Article}\n}\n\n","author_short":["Beran, M.","van Gennip, A. C. E.","Stehouwer, C. D. A.","Jansen, J. F. A.","Gupta, M. D.","Houben, A.","Berendschot, T.","Webers, C. A. B.","Wesselius, A.","Schalkwijk, C. G.","Backes, W. H.","de Jong, J. J. A.","van der Kallen, C. J. H.","van Greevenbroek, M. M. J.","Kohler, S.","Vonk, J. M. J.","Geerlings, M. I.","Schram, M. T.","van Sloten, T. T."],"key":"RN349","id":"RN349","bibbaseid":"beran-vangennip-stehouwer-jansen-gupta-houben-berendschot-webers-etal-microvasculardysfunctionandwholebrainwhitematterconnectivitythemaastrichtstudy-2024","role":"author","urls":{"Paper":"https://www.ncbi.nlm.nih.gov/pubmed/38240213"},"keyword":["cerebral microcirculation cohort diffusion tensor imaging microvascular dysfunction white matter connectivity"],"metadata":{"authorlinks":{}},"html":""},"bibtype":"article","biburl":"https://raw.githubusercontent.com/jansenjfa1/bibbase.github.io/master/jansenjfa.bib","dataSources":["TCkfRWJAZvbLAZi29"],"keywords":["cerebral microcirculation cohort diffusion tensor imaging microvascular dysfunction white matter connectivity"],"search_terms":["microvascular","dysfunction","whole","brain","white","matter","connectivity","maastricht","study","beran","van gennip","stehouwer","jansen","gupta","houben","berendschot","webers","wesselius","schalkwijk","backes","de jong","van der kallen","van greevenbroek","kohler","vonk","geerlings","schram","van sloten"],"title":"Microvascular Dysfunction and Whole-Brain White Matter Connectivity: The Maastricht Study","year":2024}