Gender- and Age-Specific Differences in Resting-State Functional Connectivity of the Central Autonomic Network in Adulthood
Open accessAbstract
Previous functional imaging studies have identified the role of central autonomic network (CAN) in autonomic regulation during various tasks. However, its variability with respect to gender and age, particularly in the resting state, remains poorly understood. Therefore, in this study we systematically investigated gender- and age-related differences in the resting-state functional connectivity (rsFC) seeded from core regions of this network, namely posterior mid-cingulate gyrus (pMCC), left amygdala, right anterior and left posterior insula, and ventromedial prefrontal cortex (vmPFC), using a large cross-sectional adulthood sample. Results revealed that each of the seeded connectivity maps engaged in at least one of the large-scale brain networks including sensorimotor, attentional, basal ganglia, limbic, and default mode networks (DMN). In the early-adulthood stage, females had stronger negative rsFC in pMCC and right anterior INS (aINS) with the medial DMN than males, possibly reflecting their greater suppression of the sympathoexcitation associated with sex hormonal estrogen. Whereas in the late-adulthood stage, they showed stronger positive rsFC in pMCC with postcentral gyrus and weaker negative rsFC with the most DMN, possibly relating to their higher risk of depression, anxiety, and dementia than males after menopause. Moreover, females demonstrated reduced negative rsFC in pMCC with dorsal PCUN/PCC and left AG with advancing age, whereas males showed the opposite pattern, namely increased positive rsFC, in pMCC with right SMG, and in vmPFC with ventral PCUN. We interpret these results as their differences of altered autonomic regulation associated with pain experience and reflective movement, respectively, due to aging. In sum, our findings add in literature that autonomic responses can be also represented intrinsically in the resting brain, and gender- and age-related differences might be associated with sex hormones and sensorimotor abilities, respectively.
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Core intrinsic connectivity networks have been associated with autonomic nervous system modulation.
“Additionally, the c-ICNs have also been associated with autonomic nervous system (ANS) modulation [45–50] possibly helping to explain the ANS dysfunction consistently reported across psychopathologies [51, 52].”
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Cites
The organization of the human cerebral cortex estimated by intrinsic functional connectivity
Thomas Yeo, B. T., Krienen, F. M., Sepulcre, J., Sabuncu, M. R., Lashkari, D., Hollinshead, M., Roffman, J. L., Smoller, J. W., Zöllei, L., Polimeni, J. R., et al. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00338.2011 · Cited by 9,182 · see citing works
The human brain is intrinsically organized into dynamic, anticorrelated functional networks
Fox, M. D., Snyder, A. Z., Vincent, J. L., Corbetta, M., Van Essen, D. C., & Raichle, M. E. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0504136102 · Cited by 8,553 · see citing works
A fast diffeomorphic image registration algorithm
Ashburner, J. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.07.007 · Cited by 8,122 · see citing works
Power, J. D., Barnes, K. A., Snyder, A. Z., Schlaggar, B. L., & Petersen, S. E. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2011.10.018 · Cited by 7,429 · see citing works
The organization of the human cerebellum estimated by intrinsic functional connectivity
Buckner, R. L., Krienen, F. M., Castellanos, A., Diaz, J. C., & Yeo, B. T. T. (2011) · Journal of Neurophysiology · doi:10.1152/jn.00339.2011 · Cited by 7,304 · see citing works
How do you feel — now? The anterior insula and human awareness
(Bud) Craig, A. D. (2009) · Nature Reviews Neuroscience · doi:10.1038/nrn2555 · Cited by 6,657 · cited 1× · see citing works
“…posterior (e.g., pMCC and pINS) and anterior (e.g., anterior MCC and aINS) functional systems that integrate multiple cognitive, homeostatic, and emotional (interoceptive) functions (Craig, 2002, 2009); and we further provide evidence of their connectivity at the resting state (Sie et al., 2019).”
BackgroundHow do you feel? Interoception: The sense of the physiological condition of the body
Craig, A. D. (2002) · Nature Reviews Neuroscience · doi:10.1038/nrn894 · Cited by 6,006 · see citing works
The precuneus: a review of its functional anatomy and behavioural correlates
Cavanna, A. E., & Trimble, M. R. (2006) · Brain · doi:10.1093/brain/awl004 · Cited by 5,128 · see citing works
A component based noise correction method (CompCor) for BOLD and perfusion based fMRI
Behzadi, Y., Restom, K., Liau, J., & Liu, T. T. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.04.042 · Cited by 4,502 · see citing works
BrainNet Viewer: A Network Visualization Tool for Human Brain Connectomics
Xia, M., Wang, J., & He, Y. (2013) · PLoS ONE · doi:10.1371/journal.pone.0068910 · Cited by 4,106 · see citing works
DPABI: Data Processing & Analysis for (Resting-State) Brain Imaging
Yan, C., Wang, X., Zuo, X., & Zang, Y. (2016) · Neuroinformatics · doi:10.1007/s12021-016-9299-4 · Cited by 3,906 · see citing works
Movement‐Related effects in fMRI time‐series
Friston, K. J., Williams, S., Howard, R., Frackowiak, R. S. J., & Turner, R. (1996) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910350312 · Cited by 3,774 · see citing works
A model of neurovisceral integration in emotion regulation and dysregulation
Thayer, J. F., & Lane, R. D. (2000) · Journal of Affective Disorders · doi:10.1016/s0165-0327(00)00338-4 · Cited by 3,092 · see citing works
Toward discovery science of human brain function
Biswal, B. B., Mennes, M., Zuo, X.-N., Gohel, S., Kelly, C., Smith, S. M., Beckmann, C. F., Adelstein, J. S., Buckner, R. L., Colcombe, S., et al. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0911855107 · Cited by 2,970 · see citing works
Murphy, K., Birn, R. M., Handwerker, D. A., Jones, T. B., & Bandettini, P. A. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2008.09.036 · Cited by 2,387 · see citing works
Satterthwaite, T., Elliott, M., Gerraty, R. T., Ruparel, K., Loughead, J., Calkins, M., Eickhoff, S., Hakonarson, H., Gur, R., Gur, R. E., et al. (2012) · NeuroImage · doi:10.1016/j.neuroimage.2012.08.052 · Cited by 1,900 · see citing works
The Central Autonomic Network: Functional Organization, Dysfunction, and Perspective
BENARROCH, E. E. (1993) · Mayo Clinic Proceedings · doi:10.1016/s0025-6196(12)62272-1 · Cited by 1,534 · see citing works
Yan, C.-G., Cheung, B., Kelly, C., Colcombe, S., Craddock, R. C., Di Martino, A., Li, Q., Zuo, X.-N., Castellanos, F. X., & Milham, M. P. (2013) · NeuroImage · doi:10.1016/j.neuroimage.2013.03.004 · Cited by 1,461 · see citing works
Human cingulate cortex and autonomic control: converging neuroimaging and clinical evidence
Critchley, H. D., Mathias, C. J., Josephs, O., O’Doherty, J., Zanini, S., Dewar, B., Cipolotti, L., Shallice, T., & Dolan, R. J. (2003) · Brain · doi:10.1093/brain/awg216 · Cited by 1,201 · see citing works
Visceral influences on brain and behavior
Critchley, H. D., & Harrison, N. A. (2013) · Neuron · doi:10.1016/j.neuron.2013.02.008 · Cited by 1,177 · see citing works
Umetani, K., Singer, D. H., McCraty, R., & Atkinson, M. (1998) · Journal of the American College of Cardiology · doi:10.1016/s0735-1097(97)00554-8 · Cited by 1,145 · see citing works
Anticorrelations in resting state networks without global signal regression
Chai, X. J., Nieto-Castañón, A., Öngür, D., & Whitfield, S. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.08.048 · Cited by 1,143 · see citing works
Beissner, F., Meissner, K., Bar, K.-J., & Napadow, V. (2013) · Journal of Neuroscience · doi:10.1523/jneurosci.1103-13.2013 · Cited by 920 · see citing works
Saad, Z. S., Gotts, S. J., Murphy, K., Chen, G., Jo, H. J., Martin, A., & Cox, R. W. (2012) · Brain Connectivity · doi:10.1089/brain.2012.0080 · Cited by 859 · see citing works
The central autonomic nervous system: conscious visceral perception and autonomic pattern generation
Saper, C. B. (2002) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.25.032502.111311 · Cited by 837 · see citing works
Functional connectivity of the insula in the resting brain
Cauda, F., D'Agata, F., Sacco, K., Duca, S., Geminiani, G., & Vercelli, A. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2010.11.049 · Cited by 793 · see citing works
Critchley, H. D., Corfield, D. R., Chandler, M. P., Mathias, C. J., & Dolan, R. J. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.t01-1-00259.x · Cited by 757 · see citing works
A Brain-Wide Study of Age-Related Changes in Functional Connectivity
Geerligs, L., Renken, R. J., Saliasi, E., Maurits, N. M., & Lorist, M. M. (2014) · Cerebral Cortex · doi:10.1093/cercor/bhu012 · Cited by 729 · see citing works
Three systems of insular functional connectivity identified with cluster analysis
Deen, B., Pitskel, N. B., & Pelphrey, K. A. (2011) · Cerebral Cortex · doi:10.1093/cercor/bhq186 · Cited by 716 · see citing works
Neural correlates of heart rate variability during emotion
Lane, R. D., Kateri Mcrae, A., Reiman, E. M., Chen, K., Ahern, G. L., & Thayer, J. F. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.07.056 · Cited by 687 · see citing works
Two systems of resting state connectivity between the insula and cingulate cortex
Taylor, K. S., Seminowicz, D. A., & Davis, K. D. (2009) · Human Brain Mapping · doi:10.1002/hbm.20705 · Cited by 665 · see citing works
Effect of aging on gender differences in neural control of heart rate
Kuo, T. B. J., Lin, T., Yang, C. C. H., Li, C.-L., Chen, C.-F., & Chou, P. (1999) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1999.277.6.h2233 · Cited by 558 · see citing works
Functional connectivity mapping of the human precuneus by resting state fMRI
Zhang, S., & Li, C.-S. R. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.11.023 · Cited by 557 · see citing works
Circadian Profile of Cardiac Autonomic Nervous Modulation in Healthy Subjects:
Bonnemeier, H., WIEGAND, U. K. H., Brandes, A., Kluge, N., Katus, H. A., Richardt, G., & Potratz, J. (2003) · Journal of Cardiovascular Electrophysiology · doi:10.1046/j.1540-8167.2003.03078.x · Cited by 532 · see citing works
Midcingulate cortex: Structure, connections, homologies, functions and diseases
Vogt, B. A. (2016) · Journal of Chemical Neuroanatomy · doi:10.1016/j.jchemneu.2016.01.010 · Cited by 471 · see citing works
Nagai, Y., Critchley, H., Featherstone, E., Trimble, M., & Dolan, R. J. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2004.01.019 · Cited by 465 · see citing works
Brain mediators of cardiovascular responses to social threat
Wager, T. D., Waugh, C. E., Lindquist, M., Noll, D. C., Fredrickson, B. L., & Taylor, S. F. (2009) · NeuroImage · doi:10.1016/j.neuroimage.2009.05.043 · Cited by 402 · see citing works
Brain activity relating to the contingent negative variation: An fMRI investigation
Nagai, Y., Critchley, H. D., Featherstone, E., Fenwick, P. B. C., Trimble, M. R., & Dolan, R. J. (2004) · NeuroImage · doi:10.1016/j.neuroimage.2003.10.036 · Cited by 377 · see citing works
Age-related changes in the default mode network are more advanced in Alzheimer disease
Jones, D. T., Machulda, M. M., Vemuri, P., McDade, E. M., Zeng, G., Senjem, M. L., Gunter, J. L., Przybelski, S. A., Avula, R. T., Knopman, D. S., et al. (2011) · Neurology · doi:10.1212/wnl.0b013e318233b33d · Cited by 370 · see citing works
Cortical Modulation of theCardiovascular System
Verberne, A. J. M., & Owens, N. C. (1998) · Progress in Neurobiology · doi:10.1016/s0301-0082(97)00056-7 · Cited by 351 · see citing works
Brain correlates of autonomic modulation: Combining heart rate variability with fMRI
Napadow, V., Dhond, R. P., Conti, G., Makris, N., Brown, E. N., & Barbieri, R. (2008) · NeuroImage · doi:10.1016/j.neuroimage.2008.04.238 · Cited by 347 · see citing works
Girgus, J. S., Yang, K., & Ferri, C. V. (2017) · Geriatrics · doi:10.3390/geriatrics2040035 · Cited by 323 · see citing works
Faster permutation inference in brain imaging
Winkler, A. M., Ridgway, G. R., Douaud, G., Nichols, T. E., & Smith, S. M. (2016) · NeuroImage · doi:10.1016/j.neuroimage.2016.05.068 · Cited by 321 · see citing works
Wang, Z., Yan, C., Zhao, C., Qi, Z., Zhou, W., Lu, J., Yong He, A., & Li, K. (2010) · Human Brain Mapping · doi:10.1002/hbm.21140 · Cited by 260 · see citing works
The human cortex responds to an interoceptive challenge
Critchley, H. D. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0401510101 · Cited by 251 · see citing works
Relation of High Heart Rate Variability to Healthy Longevity
Zulfiqar, U., Jurivich, D. A., Gao, W., & Singer, D. H. (2010) · The American Journal of Cardiology · doi:10.1016/j.amjcard.2009.12.022 · Cited by 239 · see citing works
Autonomic dysfunction in dementia
Allan, L. M., Ballard, C. G., Allen, J., Murray, A., Davidson, A. W., McKeith, I. G., & Kenny, R. A. (2006) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp.2006.102343 · Cited by 238 · see citing works
Ventral medial prefrontal cortex and cardiovagal control in conscious humans
Wong, S. W., Massé, N., Kimmerly, D. S., Menon, R. S., & Shoemaker, J. K. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2006.12.027 · Cited by 233 · see citing works
Effects of estrogen on gender-related autonomic differences in humans
Liu, C.-C., Kuo, T. B. J., & Yang, C. C. H. (2003) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00256.2003 · Cited by 233 · see citing works
Kimmerly, D. S., O’Leary, D. D., Menon, R. S., Gati, J. S., & Shoemaker, J. K. (2005) · The Journal of Physiology · doi:10.1113/jphysiol.2005.091637 · Cited by 232 · see citing works
Sex differences in normal age trajectories of functional brain networks
Scheinost, D., Finn, E. S., Tokoglu, F., Shen, X., Papademetris, X., Hampson, M., & Constable, R. T. (2014) · Human Brain Mapping · doi:10.1002/hbm.22720 · Cited by 232 · see citing works
Interaction between cognition, emotion, and the autonomic nervous system
(2013) · Handbook of Clinical Neurology · doi:10.1016/b978-0-444-53491-0.00006-7 · Cited by 230 · see citing works
Pain sensitivity and fMRI pain-related brain activity in Alzheimer's disease
Cole, L. J., Farrell, M. J., Duff, E. P., Barber, J. B., Egan, G. F., & Gibson, S. J. (2006) · Brain · doi:10.1093/brain/awl228 · Cited by 229 · see citing works
Central and autonomic nervous system integration in emotion
Hagemann, D., Waldstein, S. R., & Thayer, J. F. (2003) · Brain and Cognition · doi:10.1016/s0278-2626(03)00011-3 · Cited by 225 · see citing works
Aging, heart rate variability and patterns of autonomic regulation of the heart
Almeida-Santos, M. A., Barreto-Filho, J. A. S., Oliveira, J. L. M., Reis, F. P., Oliveira, C. C. D. C., & Sousa, A. C. S. (2015) · Archives of Gerontology and Geriatrics · doi:10.1016/j.archger.2015.11.011 · Cited by 215 · see citing works
Filippi, M., Valsasina, P., Misci, P., Falini, A., Comi, G., & Rocca, M. A. (2013) · Human Brain Mapping · doi:10.1002/hbm.21514 · Cited by 198 · see citing works
Wei, D., Zhuang, K., Ai, L., Chen, Q., Yang, W., Liu, W., Wang, K., Sun, J., & Qiu, J. (2018) · Scientific Data · doi:10.1038/sdata.2018.134 · Cited by 178 · see citing works
Sklerov, M., Dayan, E., & Browner, N. (2018) · Clinical Autonomic Research · doi:10.1007/s10286-018-0577-0 · Cited by 157 · see citing works
Ben-Shabat, E., Matyas, T. A., Pell, G. S., Brodtmann, A. G., & Carey, L. M. (2015) · Frontiers in Neurology · doi:10.3389/fneur.2015.00248 · Cited by 137 · see citing works
Central control of autonomic function and involvement in neurodegenerative disorders
(2013) · Handbook of Clinical Neurology · doi:10.1016/b978-0-444-53491-0.00005-5 · Cited by 129 · see citing works
Boubela, R. N., Kalcher, K., Huf, W., Seidel, E., Derntl, B., Pezawas, L., Našel, C., & Moser, E. (2015) · Scientific Reports · doi:10.1038/srep10499 · Cited by 129 · see citing works
Marstaller, L., Williams, M., Rich, A. N., Savage, G. R., & Burianová, H. (2015) · Neuroscience · doi:10.1016/j.neuroscience.2015.01.049 · Cited by 123 · see citing works
Parasympathetic autonomic dysfunction is common in mild cognitive impairment
Collins, O., Dillon, S., Finucane, C., LAWLOR, B. A., & Kenny, R. A. (2011) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2011.11.017 · Cited by 119 · see citing works
Williams, L. M., Brown, K. J., Das, P., Boucsein, W., Sokolov, E. N., Brammer, M. J., Olivieri, G., Peduto, A. S., & Gordon, E. (2004) · Cognitive Brain Research · doi:10.1016/j.cogbrainres.2004.06.005 · Cited by 92 · see citing works
Inspiratory loading elicits aberrant fMRI signal changes in obstructive sleep apnea
Macey, K. E., Macey, P. M., Woo, M. A., Henderson, L. A., Frysinger, R. C., Harper, R. K., Alger, J. R., Yan‐Go, F. L., & Harper, R. M. (2005) · Respiratory Physiology & Neurobiology · doi:10.1016/j.resp.2005.05.024 · Cited by 91 · see citing works
Interactions between visceral afferent signaling and stimulus processing
Critchley, H. D., & Garfinkel, S. N. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00286 · Cited by 89 · see citing works
Garza-Villarreal, E., Jiang, Z.-G., Vuust, P., Alcauter, S., Vase, L., Pasaye, E., Cavazos-Rodriguez, R., Brattico, E., Jensen, T., & Barrios, F. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.01051 · Cited by 86 · see citing works
Tian, L., Jiang, T., Liu, Y., Yu, C., Wang, K., Zhou, Y., Song, M., & Li, K. (2007) · NeuroImage · doi:10.1016/j.neuroimage.2007.03.044 · Cited by 85 · see citing works
Napadow, V., Lee, J., Kim, J., Cina, S., Maeda, Y., Barbieri, R., Harris, R. E., Kettner, N. W., & Park, K. (2012) · Human Brain Mapping · doi:10.1002/hbm.22091 · Cited by 79 · see citing works
Wong, S. W. H., Kimmerly, D. S., Massé, N., Menon, R. S., Cechetto, D. F., & Shoemaker, J. K. (2007) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00171.2007 · Cited by 77 · see citing works
Ventromedial prefrontal cortex and the regulation of physiological arousal
Zhang, S., Hu, S., Chao, H. H., Ide, J. S., Luo, X., Farr, O. M., & Li, C.-S. R. (2013) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nst064 · Cited by 76 · see citing works
Functional Imaging of Autonomic Regulation: Methods and Key Findings
Macey, P. M., Ogren, J. A., Kumar, R., & Harper, R. M. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00513 · Cited by 74 · see citing works
The relation of ventromedial prefrontal cortex activity and heart rate fluctuations at rest
Ziegler, G., Dahnke, R., Yeragani, V. K., & Bär, K. (2009) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2009.07008.x · Cited by 66 · see citing works
Acupuncture — Deep pain with an autonomic dimension?
Beißner, F., Deichmann, R., Henke, C., & Bär, K. (2011) · NeuroImage · doi:10.1016/j.neuroimage.2011.12.045 · Cited by 63 · see citing works
Resting-state functional connectivity in anterior cingulate cortex in normal aging
Cao, W., Luo, C., Zhu, B., Zhang, D., Dong, L., Gong, J., Gong, D., He, H., Tu, S., Yin, W., et al. (2014) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2014.00280 · Cited by 55 · see citing works
Heart rate variability during motor and cognitive tasks in females with major depressive disorder
Nugent, A. C., Bain, E. E., Thayer, J. F., Sollers, J. J., & Drevets, W. C. (2011) · Psychiatry Research: Neuroimaging · doi:10.1016/j.pscychresns.2010.08.013 · Cited by 54 · see citing works
He, X., Qin, W., Liu, Y., Zhang, X., Duan, Y., Song, J., Li, K., Jiang, T., & Yu, C. (2013) · Neuroscience Letters · doi:10.1016/j.neulet.2013.03.044 · Cited by 54 · see citing works
Kimmerly, D. S., Wong, S. W. H., Menon, R. S., & Shoemaker, J. K. (2006) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00366.2006 · Cited by 54 · see citing works
Representation of somatosensory inputs within the cortical autonomic network
Goswami, R., Frances, M. F., & Shoemaker, J. K. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.09.050 · Cited by 53 · see citing works
Disrupted hypothalamic functional connectivity in patients with PD and autonomic dysfunction
Dayan, E., Sklerov, M., & Browner, N. (2018) · Neurology · doi:10.1212/wnl.0000000000005641 · Cited by 53 · see citing works
Activation of central sympathetic networks during innocuous and noxious somatosensory stimulation
Maihöfner, C., Seifert, F. C., & DeCol, R. (2010) · NeuroImage · doi:10.1016/j.neuroimage.2010.11.061 · Cited by 44 · see citing works
Suzuki, H., Watanabe, S., Hamaguchi, T., Mine, H., Terui, T., Kanazawa, M., 大久典子, Maruyama, M., Yambe, T., Itoh, M., et al. (2009) · Psychosomatic Medicine · doi:10.1097/psy.0b013e31819b69ca · Cited by 40 · see citing works
Regional brain responses associated with thermogenic and psychogenic sweating events in humans
Farrell, M. J., Trevaks, D., Taylor, N. A. S., & McAllen, R. M. (2015) · Journal of Neurophysiology · doi:10.1152/jn.00601.2015 · Cited by 33 · see citing works
Altered Central Autonomic Network in Baseball Players: A Resting-state fMRI Study
Sie, J., Chen, Y.-H., Chang, C., Yen, N., Chu, W., & Shiau, Y.-H. (2019) · Scientific Reports · doi:10.1038/s41598-018-36329-9 · Cited by 22 · see citing works
Self-citationSex Differences in Insular Cortex Gyri Responses to the Valsalva Maneuver
Macey, P. M., Rieken, N. S., Kumar, R., Ogren, J. A., Middlekauff, H. R., Wu, P., Woo, M. A., & Harper, R. M. (2016) · Frontiers in Neurology · doi:10.3389/fneur.2016.00087 · Cited by 20 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Schwarz, K. G., Vicencio, S. C., Inestrosa, N. C., Villaseca, P., & Del Rio, R. (2024) · The Journal of Physiology · doi:10.1113/jp285126 · Cited by 40 · see citing works
Favieri, F., Forte, G., Pazzaglia, M., Chen, E. Y., & Casagrande, M. (2022) · Brain Sciences · doi:10.3390/brainsci12020149 · Cited by 10 · see citing works
Perez, T. M., Glue, P., Adhia, D. B., Navid, M. S., Zeng, J., Dillingham, P., Smith, M., Niazi, I. K., Young, C. K., & De Ridder, D. (2022) · Trials · doi:10.1186/s13063-022-06863-z · Cited by 8 · see citing works
- Authors
- Sie, J.-H., Chen, Y.-H., Shiau, Y.-H., & Chu, W.-C.
- Affiliations
- National Yang Ming University (TW)
- National Chengchi University (TW)
- Corresponding author
- Shiau, Yuo-Hsien
- Chu, Woei-Chyn
- ORCID
- Sie, Jia-Hong
- Venue
- Frontiers in Human Neuroscience
- Publisher
- Frontiers Media SA
- Published
- 2019-10-17
- Volume
- 13
- Pages
- 369-369
- ISSN
- 1662-5161 (ISSN-L)
- PMC
- PMC6811649
- OpenAlex
- W2980670460
- Cited by
- 35
- References
- 85
- Citations by year
- 2026: 2 · 2025: 6 · 2024: 3 · 2023: 10 · 2022: 7 · 2021: 5 · 2020: 2
- FWCI
- 2.04
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Frontiers in Human Neuroscience (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Ministry of Science and Technology, Taiwan (MOST 106-2221-E-010-012, MOST 107-2634-F-075-001)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Functional Brain Connectivity Studies
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Heart Rate Variability and Autonomic Control
- Health Sciences › Medicine › Psychiatry and Mental health › Psychosomatic Disorders and Their Treatments
- Keywords
- central autonomic network, resting-state functional connectivity, sex differences, age differences, anterior insula, amygdala, ventromedial prefrontal cortex, default mode network, autonomic regulation, estrogen, aging, menopause, sex hormones, pain experience, sensorimotor abilities
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review