References
- Zijlstra A, Mancini M, Chiari L, Zijlstra W. Biofeedback for training balance and mobility tasks in older populations: a systematic review. Journal of neuroengineering and rehabilitation. 2010;7(1):58. https://doi.org/10.1186/1743-0003-7-58
- Horlings CG, Van Engelen BG, Allum JH, Bloem BR. A weak balance: the contribution of muscle weakness to postural instability and falls. Nature Reviews Neurology. 2008;4(9):504.
- Moreland JD, Richardson JA, Goldsmith CH, Clase CM. Muscle weakness and falls in older adults: a systematic review and meta‐analysis. Journal of the American Geriatrics Society. 2004;52(7):1121-9. https://doi.org/10.1111/j.1532-5415.2004.52310.x
- Shaffer SW, Harrison AL. Aging of the somatosensory system: a translational perspective. Physical therapy. 2007;87(2):193-207. https://doi.org/10.2522/ptj.20060083
- Bugnariu N, Fung J. Aging and selective sensorimotor strategies in the regulation of upright balance. Journal of neuroengineering and rehabilitation. 2007;4(1):19. https://doi.org/10.1186/1743-0003-4-19
- Hughes S, Leary A, Zweizig S, Cain J. Surgery in elderly people: preoperative, operative and postoperative care to assist healing. Best Practice & Research Clinical Obstetrics & Gynaecology. 2013;27(5):753-65. https://doi.org/10.1016/j.bpobgyn.2013.02.006
- Cook DJ, Rooke GA. Priorities in perioperative geriatrics. Anesthesia & Analgesia. 2003;96(6):1823-36. https://doi.org/10.1213/01.ANE.0000063822.02757.41
- Robinson TN, Wu DS, Pointer LF, Dunn CL, Moss M. Preoperative cognitive dysfunction is related to adverse postoperative outcomes in the elderly. Journal of the American College of Surgeons. 2012;215(1):12-7. https://doi.org/10.1016/j.jamcollsurg.2012.02.007
- Trowbridge ER, Kim D, Barletta K, Fitz V, Larkin S, Hullfish KL. Prevalence of positive screening test for cognitive impairment among elderly urogynecologic patients. American journal of obstetrics and gynecology. 2016;215(5):663. e1-. e6. https://doi.org/10.1016/j.ajog.2016.06.012
- Williams G, Morris ME, Schache A, McCrory PR. Incidence of gait abnormalities after traumatic brain injury. Archives of physical medicine and rehabilitation. 2009;90(4):587-93. https://doi.org/10.1016/j.apmr.2008.10.013
- Lee LW, Zavarei K, Evans J, Lelas JJ, Riley PO, Kerrigan DC. Reduced hip extension in the elderly: dynamic or postural? Archives of physical medicine and rehabilitation. 2005;86(9):1851-4. https://doi.org/10.1016/j.apmr.2005.03.008
- Kim H, Park H-J, Han S-M, Hahm D-H, Lee H-J, Kim K-S, et al. The effects of acupuncture stimulation at PC6 (Neiguan) on chronic mild stress-induced biochemical and behavioral responses. Neuroscience letters. 2009;460(1):56-60. https://doi.org/10.1016/j.neulet.2009.05.008
- Samuels N, Gropp C, Singer SR, Oberbaum M. Acupuncture for psychiatric illness: a literature review. Behavioral Medicine. 2008;34(2):55-64. https://doi.org/10.3200/BMED.34.2.55-64
- Courbasson CM, de Sorkin AA, Dullerud B, Van Wyk L. Acupuncture treatment for women with concurrent substance use and anxiety/depression: an effective alternative therapy? Family & community health. 2007;30(2):112-20. https://doi.org/10.1097/01.FCH.0000264408.36013.03
- Gallagher S, Allen J, Hitt S, Schnyer R, Manber R. Six-month depression relapse rates among women treated with acupuncture. Complementary therapies in medicine. 2001;9(4):216-8. https://doi.org/10.1054/ctim.2001.0470
- Pilkington K. Acupuncture therapy for psychiatric illness. International review of neurobiology. 111: Elsevier; 2013. p. 197-216. https://doi.org/10.1016/B978-0-12-411545-3.00010-9
- Zeng B-Y, Salvage S, Jenner P. Effect and mechanism of acupuncture on Alzheimer's disease. International review of neurobiology. 111: Elsevier; 2013. p. 181-95. https://doi.org/10.1016/B978-0-12-411545-3.00009-2
- Napadow V, Makris N, Liu J, Kettner NW, Kwong KK, Hui KK. Effects of electroacupuncture versus manual acupuncture on the human brain as measured by fMRI. Human brain mapping. 2005;24(3):193-205. https://doi.org/10.1002/hbm.20081
- Napadow V, Dhond R, Purdon P, Kettner N, Makris N, Kwong K, et al., editors. Correlating acupuncture FMRI in the human brainstem with heart rate variability. 2005 IEEE Engineering in Medicine and Biology 27th Annual Conference; 2006: IEEE.
- Dhond RP, Yeh C, Park K, Kettner N, Napadow V. Acupuncture modulates resting state connectivity in default and sensorimotor brain networks. Pain. 2008;136(3):407-18. https://doi.org/10.1016/j.pain.2008.01.011
- Harvie C, Weissbart SJ, Kadam‐Halani P, Rao H, Arya LA. Brain Activation during the Voiding phase of Micturition in Healthy Adults: A Meta‐analysis of Neuroimaging Studies. Clinical Anatomy. 2018.
- Osman NI, Chapple CR. Contemporary concepts in the aetiopathogenesis of detrusor underactivity. Nature Reviews Urology. 2014;11(11):639. https://doi.org/10.1038/nrurol.2014.286
- Abarbanel J, Marcus E-L. Impaired detrusor contractility in community-dwelling elderly presenting with lower urinary tract symptoms. Urology. 2007;69(3):436-40. https://doi.org/10.1016/j.urology.2006.11.019
- Resnick NM, Brandeis GH, Baumann MM, DuBeau CE, Yalla SV. Misdiagnosis of urinary incontinence in nursing home women: prevalence and a proposed solution. Neurourology and Urodynamics: Official Journal of the International Continence Society. 1996;15(6):599-618. https://doi.org/10.1002/(SICI)1520-6777(1996)15:6<599::AID-NAU2>3.0.CO;2-A
- Osman NI, Chapple CR. Fowler's syndrome-a cause of unexplained urinary retention in young women? Nature Reviews Urology. 2014;11(2):87. https://doi.org/10.1038/nrurol.2013.277
- Holstege G, Griffiths D, De Wall H, Dalm E. Anatomical and physiological observations on suprapinal control of bladder and urethral sphincter muscles in the cat. Journal of Comparative Neurology. 1986;250(4):449-61. https://doi.org/10.1002/cne.902500404
- Arya NG, Weissbart SJ, Xu S, Rao H. Brain activation in response to bladder filling in healthy adults: An activation likelihood estimation meta‐analysis of neuroimaging studies. Neurourology and urodynamics. 2017;36(4):960-5. https://doi.org/10.1002/nau.23058
- Griffiths D, Fowler C. The micturition switch and its forebrain influences. Acta physiologica. 2013;207(1):93-109. https://doi.org/10.1111/apha.12019
- Arya NG, Weissbart SJ. Central control of micturition in women: Brain-bladder pathways in continence and urgency urinary incontinence. Clinical anatomy (New York, NY). 2017;30(3):373-84. https://doi.org/10.1002/ca.22840
- Harvie C, Weissbart SJ, Kadam-Halani P, Rao H, Arya LA. Brain activation during the voiding phase of micturition in healthy adults: A meta-analysis of neuroimaging studies. Clinical anatomy (New York, NY). 2018.
- Griffiths D, Tadic SD, Schaefer W, Resnick NM. Cerebral control of the bladder in normal and urge-incontinent women. NeuroImage. 2007;37(1):1-7. https://doi.org/10.1016/j.neuroimage.2007.04.061
- Komesu YM, Ketai LH, Mayer AR, Teshiba TM, Rogers RG. Functional MRI of the Brain in Women with Overactive Bladder: Brain Activation During Urinary Urgency. Female pelvic medicine & reconstructive surgery. 2011;17(1):50-4. https://doi.org/10.1097/SPV.0b013e3182065507
- Craig AD. How do you feel? Interoception: the sense of the physiological condition of the body. Nature reviews Neuroscience. 2002;3(8):655-66. https://doi.org/10.1038/nrn894
- Bush G, Luu P, Posner MI. Cognitive and emotional influences in anterior cingulate cortex. Trends in cognitive sciences. 2000;4(6):215-22. https://doi.org/10.1016/S1364-6613(00)01483-2
- Blok BF, Willemsen AT, Holstege G. A PET study on brain control of micturition in humans. Brain : a journal of neurology. 1997;120 ( Pt 1):111-21. https://doi.org/10.1093/brain/120.1.111
- Blok BF, Sturms LM, Holstege G. Brain activation during micturition in women. Brain : a journal of neurology. 1998;121 ( Pt 11):2033-42. https://doi.org/10.1093/brain/121.11.2033
- Michels L, Blok BF, Gregorini F, Kurz M, Schurch B, Kessler TM, et al. Supraspinal Control of Urine Storage and Micturition in Men--An fMRI Study. Cerebral cortex (New York, NY : 1991). 2015;25(10):3369-80. https://doi.org/10.1093/cercor/bhu140
- Rossi AF, Pessoa L, Desimone R, Ungerleider LG. The prefrontal cortex and the executive control of attention. Experimental brain research. 2009;192(3):489-97. https://doi.org/10.1007/s00221-008-1642-z
- Arya NG, Weissbart SJ, Xu S, Rao H. Brain activation in response to bladder filling in healthy adults: An activation likelihood estimation meta-analysis of neuroimaging studies. Neurourol Urodyn. 2017;36(4):960-5. https://doi.org/10.1002/nau.23058
- Sakakibara R, Uchida Y, Uchiyama T, Yamanishi T, Hattori T. Reduced cerebellar vermis activation during urinary storage and micturition in multiple system atrophy: 99mTc-labelled ECD SPECT study. European journal of neurology. 2004;11(10):705-8. https://doi.org/10.1111/j.1468-1331.2004.00872.x
- Clarkson BD, Karim HT, Griffiths DJ, Resnick NM. Functional connectivity of the brain in older women with urgency urinary incontinence. Neurourol Urodyn. 2018;37(8):2763-75. https://doi.org/10.1002/nau.23766
- Griffiths D, Clarkson B, Tadic SD, Resnick NM. Brain Mechanisms Underlying Urge Incontinence and its Response to Pelvic Floor Muscle Training. J Urol. 2015;194(3):708-15. https://doi.org/10.1016/j.juro.2015.03.102
- Reshef E, Lei ZM, Rao CV, Pridham DD, Chegini N, Luborsky JL. The presence of gonadotropin receptors in nonpregnant human uterus, human placenta, fetal membranes, and decidua. The Journal of clinical endocrinology and metabolism. 1990;70(2):421-30. https://doi.org/10.1210/jcem-70-2-421
- Lei ZM, Rao CV, Kornyei JL, Licht P, Hiatt ES. Novel expression of human chorionic gonadotropin/luteinizing hormone receptor gene in brain. Endocrinology. 1993;132(5):2262-70. https://doi.org/10.1210/endo.132.5.8477671
- AA AL-H, Lei ZM, Rao CV. Neurons from fetal rat brains contain functional luteinizing hormone/chorionic gonadotropin receptors. Biology of reproduction. 1997;56(5):1071-6. https://doi.org/10.1095/biolreprod56.5.1071
- Tao YX, Lei ZM, Hofmann GE, Rao CV. Human intermediate trophoblasts express chorionic gonadotropin/luteinizing hormone receptor gene. Biology of reproduction. 1995;53(4):899-904. https://doi.org/10.1095/biolreprod53.4.899
- Gawronska B, Paukku T, Huhtaniemi I, Wasowicz G, Ziecik AJ. Oestrogen-dependent expression of LH/hCG receptors in pig Fallopian tube and their role in relaxation of the oviduct. Journal of reproduction and fertility. 1999;115(2):293-301. https://doi.org/10.1530/jrf.0.1150293
- Wasowicz G, Derecka K, Stepien A, Pelliniemi L, Doboszynska T, Gawronska B, et al. Evidence for the presence of luteinizing hormone-chorionic gonadotrophin receptors in the pig umbilical cord. Journal of reproduction and fertility. 1999;117(1):1-9. https://doi.org/10.1530/jrf.0.1170001
- Bukovsky A, Chen TT, Wimalasena J, Caudle MR. Cellular localization of luteinizing hormone receptor immunoreactivity in the ovaries of immature, gonadotropin-primed and normal cycling rats. Biology of reproduction. 1993;48(6):1367-82. https://doi.org/10.1095/biolreprod48.6.1367
- Zhang YM, Rao Ch V, Lei ZM. Macrophages in human reproductive tissues contain luteinizing hormone/chorionic gonadotropin receptors. American journal of reproductive immunology (New York, NY : 1989). 2003;49(2):93-100. https://doi.org/10.1034/j.1600-0897.2003.00013.x
- Gawronska B, Leuschner C, Enright FM, Hansel W. Effects of a lytic peptide conjugated to beta HCG on ovarian cancer: studies in vitro and in vivo. Gynecologic oncology. 2002;85(1):45-52. https://doi.org/10.1006/gyno.2001.6558
- Liu B, Hong JS. Role of microglia in inflammation-mediated neurodegenerative diseases: mechanisms and strategies for therapeutic intervention. The Journal of pharmacology and experimental therapeutics. 2003;304(1):1-7. https://doi.org/10.1124/jpet.102.035048
- Nakamura Y. Regulating factors for microglial activation. Biological & pharmaceutical bulletin. 2002;25(8):945-53. https://doi.org/10.1248/bpb.25.945
- Hershkovitz R, Erez O, Sheiner E, Landau D, Mankuta D, Mazor M. Elevated maternal mid-trimester chorionic gonadotropin > or =4 MoM is associated with fetal cerebral blood flow redistribution. Acta obstetricia et gynecologica Scandinavica. 2003;82(1):22-7. https://doi.org/10.1080/j.1600-0412.2003.820104.x
- Fillit H. Estrogens in the pathogenesis and treatment of Alzheimer's disease in postmenopausal women. Annals of the New York Academy of Sciences. 1994;743:233-8; discussion 8-9.
- Green PS, Simpkins JW. Estrogens and estrogen-like non-feminizing compounds. Their role in the prevention and treatment of Alzheimer's disease. Annals of the New York Academy of Sciences. 2000;924:93-8. https://doi.org/10.1111/j.1749-6632.2000.tb05566.x
- Monk D, Brodaty H. Use of estrogens for the prevention and treatment of Alzheimer's disease. Dementia and geriatric cognitive disorders. 2000;11(1):1-10. https://doi.org/10.1159/000017206
-
Schafer A, Pauli G, Friedmann W, Dudenhausen JW. Human choriogonadotropin (hCG) and placental lactogen (hPL) inhibit interleukin-2 (IL-2) and increase interleukin-
$1{\beta}$ (IL-$1{\beta}$ ),-6 (IL-6) and tumor necrosis factor ($TNF-{\alpha}$ ) expression in monocyte cell cultures. Journal of Perinatal Medicine-Official Journal of the WAPM. 1992;20(3):233-40. https://doi.org/10.1515/jpme.1992.20.3.233 - Reinisch N, Sitte B, Kahler C, Wiedermann C. Human chorionic gonadotrophin: a chemoattractant for human blood monocytes, neutrophils and lymphocytes. Journal of endocrinology. 1994;142(1):167-70. https://doi.org/10.1677/joe.0.1420167
- Shirshev S, Lyalina O, Zamorina S. Role of potassium ions in monocyte-regulating effects of chorionic gonadotropin. Bulletin of experimental biology and medicine. 2000;130(5):1099. https://doi.org/10.1007/BF02688190
- Kosaka K, Fujiwara H, Tatsumi K, Yoshioka S, Sato Y, Egawa H, et al. Human chorionic gonadotropin (HCG) activates monocytes to produce interleukin-8 via a different pathway from luteinizing hormone/HCG receptor system. The Journal of Clinical Endocrinology & Metabolism. 2002;87(11):5199-208. https://doi.org/10.1210/jc.2002-020341
- Bukovsky A, Indrapichate K, Fujiwara H, Cekanova M, Ayala ME, Dominguez R, et al. Multiple luteinizing hormone receptor (LHR) protein variants, interspecies reactivity of anti-LHR mAb clone 3B5, subcellular localization of LHR in human placenta, pelvic floor and brain, and possible role for LHR in the development of abnormal pregnancy, pelvic floor disorders and Alzheimer's disease. Reproductive Biology and Endocrinology. 2003;1(1):46. https://doi.org/10.1186/1477-7827-1-46
- Castelan F, Lopez‐Garcia K, Moreno‐Perez S, Zempoalteca R, Corona‐Quintanilla DL, Romero‐Ortega MI, et al. Multiparity affects conduction properties of pelvic floor nerves in rabbits. Brain and behavior. 2018;8(10):e01105. https://doi.org/10.1002/brb3.1105
- de Aguiar Cavalcanti G, Manzano GM, Nunes KF, Giuliano LMP, de Menezes TA, Bruschini H. Electrophysiological evaluation of the pudendal nerve and urethral innervation in female stress urinary incontinence. International urogynecology journal. 2013;24(5):801-7. https://doi.org/10.1007/s00192-012-1931-8
- Elser DM. Stress urinary incontinence and overactive bladder syndrome: current options and new targets for management. Postgraduate medicine. 2012;124(3):42-9. https://doi.org/10.3810/pgm.2012.05.2547
- Clemens JQ, Mullins C, Kusek JW, Kirkali Z, Mayer EA, Rodriguez LV, et al. The MAPP research network: a novel study of urologic chronic pelvic pain syndromes. BMC urology. 2014;14(1):57. https://doi.org/10.1186/1471-2490-14-57
- Allsop SA, Erstad DJ, Brook K, Bhai SF, Cohen JM, Dimitrakoff JD. The DABBEC phenotyping system: towards a mechanistic understanding of CP/CPPS. Nature reviews Urology. 2011;8(2):107. https://doi.org/10.1038/nrurol.2010.227
- Hanno P, Andersson KE, Birder L, Elneil S, Kanai A, Pontari M. Chronic pelvic pain syndrome/bladder pain syndrome: Taking stock, looking ahead: ICI‐RS 2011. Neurourology and urodynamics. 2012;31(3):375-83. https://doi.org/10.1002/nau.22202
- Nicke JC. A new approach to understanding and managing chronic prostatitis and interstitial cystitis. Reviews in urology. 2010;12(1):67.
- Shoskes D, Nickel J, Rackley R, Pontari M. Clinical phenotyping in chronic prostatitis/chronic pelvic pain syndrome and interstitial cystitis: a management strategy for urologic chronic pelvic pain syndromes. Prostate cancer and prostatic diseases. 2009;12(2):177. https://doi.org/10.1038/pcan.2008.42
- Lai HH, North CS, Andriole GL, Sayuk GS, Hong BA. Polysymptomatic, polysyndromic presentation of patients with urological chronic pelvic pain syndrome. The Journal of urology. 2012;187(6):2106-12. https://doi.org/10.1016/j.juro.2012.01.081
- Dimitrakov J, Guthrie D. Genetics and phenotyping of urological chronic pelvic pain syndrome. The Journal of urology. 2009;181(4):1550-7. https://doi.org/10.1016/j.juro.2008.11.119
- Farmer MA, Chanda ML, Parks EL, Baliki MN, Apkarian AV, Schaeffer AJ. Brain functional and anatomical changes in chronic prostatitis/chronic pelvic pain syndrome. The Journal of urology. 2011;186(1):117-24. https://doi.org/10.1016/j.juro.2011.03.027
- Chen JY-W, Blankstein U, Diamant NE, Davis KD. White matter abnormalities in irritable bowel syndrome and relation to individual factors. Brain research. 2011;1392:121-31. https://doi.org/10.1016/j.brainres.2011.03.069
- Ellingson BM, Mayer E, Harris RJ, Ashe-McNally C, Naliboff BD, Labus JS, et al. Diffusion tensor imaging detects microstructural reorganization in the brain associated with chronic irritable bowel syndrome. PAIN(R). 2013;154(9):1528-41. https://doi.org/10.1016/j.pain.2013.04.010
- Grachev ID, Fredrickson BE, Apkarian AV. Abnormal brain chemistry in chronic back pain: an in vivo proton magnetic resonance spectroscopy study. Pain. 2000;89(1):7-18. https://doi.org/10.1016/S0304-3959(00)00340-7
- Apkarian AV, Sosa Y, Sonty S, Levy RM, Harden RN, Parrish TB, et al. Chronic back pain is associated with decreased prefrontal and thalamic gray matter density. Journal of neuroscience. 2004;24(46):10410-5. https://doi.org/10.1523/JNEUROSCI.2541-04.2004
- Baliki MN, Chialvo DR, Geha PY, Levy RM, Harden RN, Parrish TB, et al. Chronic pain and the emotional brain: specific brain activity associated with spontaneous fluctuations of intensity of chronic back pain. Journal of Neuroscience. 2006;26(47):12165-73. https://doi.org/10.1523/JNEUROSCI.3576-06.2006
- Frokjær JB, Olesen SS, Gram M, Yavarian Y, Bouwense SA, Wilder-Smith OH, et al. Altered brain microstructure assessed by diffusion tensor imaging in patients with chronic pancreatitis. Gut. 2011;60(11):1554-62. https://doi.org/10.1136/gut.2010.236620
- Geha PY, Baliki MN, Harden RN, Bauer WR, Parrish TB, Apkarian AV. The brain in chronic CRPS pain: abnormal gray-white matter interactions in emotional and autonomic regions. Neuron. 2008;60(4):570-81. https://doi.org/10.1016/j.neuron.2008.08.022
- Landis JR, Williams DA, Lucia MS, Clauw DJ, Naliboff BD, Robinson NA, et al. The MAPP research network: design, patient characterization and operations. BMC urology. 2014;14(1):58. https://doi.org/10.1186/1471-2490-14-58
- Woodworth D, Mayer E, Leu K, Ashe-McNalley C, Naliboff BD, Labus JS, et al. Unique Microstructural Changes in the Brain Associated with Urological Chronic Pelvic Pain Syndrome (UCPPS) Revealed by Diffusion Tensor MRI, Super-Resolution Track Density Imaging, and Statistical Parameter Mapping: A MAPP Network Neuroimaging Study. PloS one. 2015;10(10):e0140250. https://doi.org/10.1371/journal.pone.0140250
- Harper DE, Ichesco E, Schrepf A, Halvorson M, Puiu T, Clauw DJ, et al. Relationships between brain metabolite levels, functional connectivity, and negative mood in urologic chronic pelvic pain syndrome patients compared to controls: A MAPP research network study. NeuroImage Clinical. 2018;17:570-8. https://doi.org/10.1016/j.nicl.2017.11.014
- Kilpatrick LA, Kutch JJ, Tillisch K, Naliboff BD, Labus JS, Jiang Z, et al. Alterations in resting state oscillations and connectivity in sensory and motor networks in women with interstitial cystitis/painful bladder syndrome. J Urol. 2014;192(3):947-55. https://doi.org/10.1016/j.juro.2014.03.093
- Kleinhans NM, Yang CC, Strachan ED, Buchwald DS, Maravilla KR. Alterations in Connectivity on Functional Magnetic Resonance Imaging with Provocation of Lower Urinary Tract Symptoms: A MAPP Research Network Feasibility Study of Urological Chronic Pelvic Pain Syndromes. J Urol. 2016;195(3):639-45. https://doi.org/10.1016/j.juro.2015.09.092
- Kutch JJ, Labus JS, Harris RE, Martucci KT, Farmer MA, Fenske S, et al. Resting-state functional connectivity predicts longitudinal pain symptom change in urologic chronic pelvic pain syndrome: a MAPP network study. Pain. 2017;158(6):1069-82. https://doi.org/10.1097/j.pain.0000000000000886
- Kutch JJ, Yani MS, Asavasopon S, Kirages DJ, Rana M, Cosand L, et al. Altered resting state neuromotor connectivity in men with chronic prostatitis/chronic pelvic pain syndrome: A MAPP: Research Network Neuroimaging Study. NeuroImage Clinical. 2015;8:493-502. https://doi.org/10.1016/j.nicl.2015.05.013
- Martucci KT, Shirer WR, Bagarinao E, Johnson KA, Farmer MA, Labus JS, et al. The posterior medial cortex in urologic chronic pelvic pain syndrome: detachment from default mode network-a resting-state study from the MAPP Research Network. Pain. 2015;156(9):1755-64. https://doi.org/10.1097/j.pain.0000000000000238
- As-Sanie S, Kim J, Schmidt-Wilcke T, Sundgren PC, Clauw DJ, Napadow V, et al. Functional Connectivity is Associated With Altered Brain Chemistry in Women With Endometriosis-Associated Chronic Pelvic Pain. The journal of pain : official journal of the American Pain Society. 2016;17(1):1-13. https://doi.org/10.1016/j.jpain.2015.09.008
- Clauw DJ, Schmidt M, Radulovic D, Singer A, Katz P, Bresette J. The relationship between fibromyalgia and interstitial cystitis. Journal of psychiatric research. 1997;31(1):125-31. https://doi.org/10.1016/S0022-3956(96)00051-9
- Grinberg K, Granot M, Lowenstein L, Abramov L, Weissman-Fogel I. A common pronociceptive pain modulation profile typifying subgroups of chronic pelvic pain syndromes is interrelated with enhanced clinical pain. Pain. 2017;158(6):1021-9. https://doi.org/10.1097/j.pain.0000000000000869
- Iacovides S, Avidon I, Baker FC. Women with dysmenorrhoea are hypersensitive to experimentally induced forearm ischaemia during painful menstruation and during the pain-free follicular phase. European journal of pain (London, England). 2015;19(6):797-804. https://doi.org/10.1002/ejp.604
- Ness TJ, Powell-Boone T, Cannon R, Lloyd LK, Fillingim RB. Psychophysical evidence of hypersensitivity in subjects with interstitial cystitis. The Journal of urology. 2005;173(6):1983-7. https://doi.org/10.1097/01.ju.0000158452.15915.e2
- Ness TJ, Lloyd LK, Fillingim RB. An endogenous pain control system is altered in subjects with interstitial cystitis. The Journal of urology. 2014;191(2):364-70. https://doi.org/10.1016/j.juro.2013.08.024
- Powell-Boone T, Ness TJ, Cannon R, Lloyd LK, Weigent DA, Fillingim RB. Menstrual cycle affects bladder pain sensation in subjects with interstitial cystitis. The Journal of urology. 2005;174(5):1832-6. https://doi.org/10.1097/01.ju.0000176747.40242.3d
- Slater H, Paananen M, Smith AJ, O'Sullivan P, Briggs AM, Hickey M, et al. Heightened cold pain and pressure pain sensitivity in young female adults with moderate-to-severe menstrual pain. Pain. 2015;156(12):2468-78. https://doi.org/10.1097/j.pain.0000000000000317
- Stratton P, Khachikyan I, Sinaii N, Ortiz R, Shah J. Association of chronic pelvic pain and endometriosis with signs of sensitization and myofascial pain. Obstetrics and gynecology. 2015;125(3):719-28. https://doi.org/10.1097/AOG.0000000000000663
- Aguila MR, Rebbeck T, Leaver AM, Lagopoulos J, Brennan PC, Hubscher M, et al. The Association Between Clinical Characteristics of Migraine and Brain GABA Levels: An Exploratory Study. The journal of pain : official journal of the American Pain Society. 2016;17(10):1058-67. https://doi.org/10.1016/j.jpain.2016.06.008
- Cao B, Stanley JA, Selvaraj S, Mwangi B, Passos IC, Zunta-Soares GB, et al. Evidence of altered membrane phospholipid metabolism in the anterior cingulate cortex and striatum of patients with bipolar disorder I: A multi-voxel (1)H MRS study. Journal of psychiatric research. 2016;81:48-55. https://doi.org/10.1016/j.jpsychires.2016.06.006
- Chang L, Munsaka SM, Kraft-Terry S, Ernst T. Magnetic resonance spectroscopy to assess neuroinflammation and neuropathic pain. Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology. 2013;8(3):576-93. https://doi.org/10.1007/s11481-013-9460-x
- Fayed N, Garcia-Campayo J, Magallon R, Andres-Bergareche H, Luciano JV, Andres E, et al. Localized 1H-NMR spectroscopy in patients with fibromyalgia: a controlled study of changes in cerebral glutamate/glutamine, inositol, choline, and N-acetylaspartate. Arthritis research & therapy. 2010;12(4):R134. https://doi.org/10.1186/ar3072
- Feraco P, Bacci A, Pedrabissi F, Passamonti L, Zampogna G, Pedrabissi F, et al. Metabolic abnormalities in pain-processing regions of patients with fibromyalgia: a 3T MR spectroscopy study. AJNR American journal of neuroradiology. 2011;32(9):1585-90. https://doi.org/10.3174/ajnr.A2550
- Foerster BR, Petrou M, Edden RA, Sundgren PC, Schmidt-Wilcke T, Lowe SE, et al. Reduced insular gamma-aminobutyric acid in fibromyalgia. Arthritis and rheumatism. 2012;64(2):579-83. https://doi.org/10.1002/art.33339
- Harris RE, Clauw DJ. Imaging central neurochemical alterations in chronic pain with proton magnetic resonance spectroscopy. Neuroscience letters. 2012;520(2):192-6. https://doi.org/10.1016/j.neulet.2012.03.042
- Harris RE, Napadow V, Huggins JP, Pauer L, Kim J, Hampson J, et al. Pregabalin rectifies aberrant brain chemistry, connectivity, and functional response in chronic pain patients. Anesthesiology. 2013;119(6):1453-64. https://doi.org/10.1097/ALN.0000000000000017
- Harris RE, Sundgren PC, Craig AD, Kirshenbaum E, Sen A, Napadow V, et al. Elevated insular glutamate in fibromyalgia is associated with experimental pain. Arthritis and rheumatism. 2009;60(10):3146-52. https://doi.org/10.1002/art.24849
- Harris RE, Sundgren PC, Pang Y, Hsu M, Petrou M, Kim SH, et al. Dynamic levels of glutamate within the insula are associated with improvements in multiple pain domains in fibromyalgia. Arthritis and rheumatism. 2008;58(3):903-7. https://doi.org/10.1002/art.23223
- Ito T, Tanaka-Mizuno S, Iwashita N, Tooyama I, Shiino A, Miura K, et al. Proton magnetic resonance spectroscopy assessment of metabolite status of the anterior cingulate cortex in chronic pain patients and healthy controls. Journal of pain research. 2017;10:287-93. https://doi.org/10.2147/JPR.S123403
- Petrou M, Harris RE, Foerster BR, McLean SA, Sen A, Clauw DJ, et al. Proton MR spectroscopy in the evaluation of cerebral metabolism in patients with fibromyalgia: comparison with healthy controls and correlation with symptom severity. AJNR American journal of neuroradiology. 2008;29(5):913-8. https://doi.org/10.3174/ajnr.A0959
- Petrou M, Pop-Busui R, Foerster BR, Edden RA, Callaghan BC, Harte SE, et al. Altered excitation-inhibition balance in the brain of patients with diabetic neuropathy. Academic radiology. 2012;19(5):607-12. https://doi.org/10.1016/j.acra.2012.02.004
- Reckziegel D, Raschke F, Cottam WJ, Auer DP. Cingulate GABA levels inversely correlate with the intensity of ongoing chronic knee osteoarthritis pain. Molecular pain. 2016;12.
- Valdes M, Collado A, Bargallo N, Vazquez M, Rami L, Gomez E, et al. Increased glutamate/glutamine compounds in the brains of patients with fibromyalgia: a magnetic resonance spectroscopy study. Arthritis and rheumatism. 2010;62(6):1829-36. https://doi.org/10.1002/art.27430
- Widerstrom-Noga E, Pattany PM, Cruz-Almeida Y, Felix ER, Perez S, Cardenas DD, et al. Metabolite concentrations in the anterior cingulate cortex predict high neuropathic pain impact after spinal cord injury. Pain. 2013;154(2):204-12. https://doi.org/10.1016/j.pain.2012.07.022
- Zhao X, Xu M, Jorgenson K, Kong J. Neurochemical changes in patients with chronic low back pain detected by proton magnetic resonance spectroscopy: A systematic review. NeuroImage Clinical. 2017;13:33-8. https://doi.org/10.1016/j.nicl.2016.11.006
- Bagarinao E, Johnson KA, Martucci KT, Ichesco E, Farmer MA, Labus J, et al. Preliminary structural MRI based brain classification of chronic pelvic pain: A MAPP network study. Pain. 2014;155(12):2502-9. https://doi.org/10.1016/j.pain.2014.09.002
- Farmer MA, Huang L, Martucci K, Yang CC, Maravilla KR, Harris RE, et al. Brain White Matter Abnormalities in Female Interstitial Cystitis/Bladder Pain Syndrome: A MAPP Network Neuroimaging Study. The Journal of urology. 2015;194(1):118-26. https://doi.org/10.1016/j.juro.2015.02.082
- Mayer EA, Gupta A, Kilpatrick LA, Hong JY. Imaging brain mechanisms in chronic visceral pain. Pain. 2015;156 Suppl 1:S50-63. https://doi.org/10.1097/j.pain.0000000000000106
- Kuner R, Flor H. Structural plasticity and reorganisation in chronic pain. Nature reviews Neuroscience. 2016;18(1):20-30. https://doi.org/10.1038/nrn.2016.162
- Maixner W, Fillingim RB, Williams DA, Smith SB, Slade GD. Overlapping Chronic Pain Conditions: Implications for Diagnosis and Classification. The journal of pain : official journal of the American Pain Society. 2016;17(9 Suppl):T93-t107. https://doi.org/10.1016/j.jpain.2016.06.002
- Schmidt-Wilcke T. Neuroimaging of chronic pain. Best practice & research Clinical rheumatology. 2015;29(1):29-41. https://doi.org/10.1016/j.berh.2015.04.030
- Walitt B, Ceko M, Gracely JL, Gracely RH. Neuroimaging of Central Sensitivity Syndromes: Key Insights from the Scientific Literature. Current rheumatology reviews. 2016;12(1):55-87. https://doi.org/10.2174/1573397112666151231111104
- Huang L, Kutch JJ, Ellingson BM, Martucci KT, Harris RE, Clauw DJ, et al. Brain white matter changes associated with urological chronic pelvic pain syndrome: multisite neuroimaging from a MAPP case-control study. Pain. 2016;157(12):2782-91. https://doi.org/10.1097/j.pain.0000000000000703
- Kairys AE, Schmidt-Wilcke T, Puiu T, Ichesco E, Labus JS, Martucci K, et al. Increased brain gray matter in the primary somatosensory cortex is associated with increased pain and mood disturbance in patients with interstitial cystitis/painful bladder syndrome. The Journal of urology. 2015;193(1):131-7. https://doi.org/10.1016/j.juro.2014.08.042
- Deutsch G, Deshpande H, Frolich MA, Lai HH, Ness TJ. Bladder Distension Increases Blood Flow in Pain Related Brain Structures in Subjects with Interstitial Cystitis. The Journal of urology. 2016;196(3):902-10. https://doi.org/10.1016/j.juro.2016.03.135
- Siedentopf CM, Golaszewski SM, Mottaghy FM, Ruff CC, Felber S, Schlager A. Functional magnetic resonance imaging detects activation of the visual association cortex during laser acupuncture of the foot in humans. Neuroscience letters. 2002;327(1):53-6. https://doi.org/10.1016/S0304-3940(02)00383-X
- Siedentopf CM, Koppelstaetter F, Haala IA, Haid V, Rhomberg P, Ischebeck A, et al. Laser acupuncture induced specific cerebral cortical and subcortical activations in humans. Lasers in medical science. 2005;20(2):68-73. https://doi.org/10.1007/s10103-005-0340-3
- Napadow V, Makris N, Liu J, Kettner NW, Kwong KK, Hui KK. Effects of electroacupuncture versus manual acupuncture on the human brain as measured by fMRI. Human brain mapping. 2005;24(3):193-205. https://doi.org/10.1002/hbm.20081
- Biella G, Sotgiu ML, Pellegata G, Paulesu E, Castiglioni I, Fazio F. Acupuncture produces central activations in pain regions. NeuroImage. 2001;14(1 Pt 1):60-6. https://doi.org/10.1006/nimg.2001.0798
- Hui KK, Liu J, Makris N, Gollub RL, Chen AJ, Moore CI, et al. Acupuncture modulates the limbic system and subcortical gray structures of the human brain: evidence from fMRI studies in normal subjects. Human brain mapping. 2000;9(1):13-25. https://doi.org/10.1002/(SICI)1097-0193(2000)9:1<13::AID-HBM2>3.0.CO;2-F
- Lv J, Shi C, Deng Y, Lou W, Hu J, Shi L, et al. The brain effects of laser acupuncture at thirteen ghost acupoints in healthy individuals: A resting-state functional MRI investigation. Computerized medical imaging and graphics : the official journal of the Computerized Medical Imaging Society. 2016;54:48-54. https://doi.org/10.1016/j.compmedimag.2016.08.003
- Zhang S, Li CS. A neural measure of behavioral engagement: task-residual low-frequency blood oxygenation level-dependent activity in the precuneus. NeuroImage. 2010;49(2):1911-8. https://doi.org/10.1016/j.neuroimage.2009.09.004
- Rosazza C, Minati L. Resting-state brain networks: literature review and clinical applications. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. 2011;32(5):773-85. https://doi.org/10.1007/s10072-011-0636-y