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Pharmacogenomics Volume 8, 2007 - Issue 1
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Review

The Genetics of Fibromyalgia Syndrome

Dan Buskila1 Ben Gurion University, Department of Medicine H, Soroka Medical Center and Faculty of Health Sciences, Beer Sheva, Israel. [email protected]
,
Piercarlo Sarzi-Puttini2 L Sacco University Hospital, Senior Rheumatologist, Rheumatology Unit, Via GB Grassi 74, 20157Milano, Italy. [email protected]
&
Jacob N Ablin3 Tel-Aviv University, Departments of Rheumatology, Tel-Aviv Sourasky Medical Center and Sackler Faculty of Medicine, Tel-Aviv, Israel. [email protected]
Pages 67-74 | Published online: 22 Dec 2006

Bibliography

  • Wolfe F , SmytheH, YunusMB et al.: The American College of Rheumatology 1990 criteria for the classification of fibromyalgia. Report of the multicenter criteria committee. Arthritis Rheum.33(2), 160–172 (1990).
  • Mease P : Fibromyalgia syndrome: review of clinical presentation, pathogenesis, outcome measures, and treatment.J. Rheumatol. Suppl.75, 6–21 (2005).
  • Buskila D , NeumannL, PressJ: Genetic factors in neuromusclar pain.CNS Spectrums10(4), 281–284 (2005).
  • Buskila D , NeumannL: Genetics of fibromyalgia.Curr. Pain Headache Res.9(5), 313–315 (2005).
  • Clauw DJ , CroffordL: Chronic widespread pain and fibromyalgia: what we know, and what we need to know.Best Pract. Res. Clin. Rheumatol.17(4), 685–701 (2003).
  • Buskila D , NeumannL, HazanovI, Carmi R: Familial aggregation in the fibromyalgia syndrome. Semin. Arthritis Rheum.26(3), 605–611 (1996).
  • Buskila D , NeumannL: Fibromyalgia syndrome (FM) and nonarticular tenderness in relatives of patients with FM.J. Rheumatol.24(5), 941–944 (1997).
  • Arnold LM , HudsonJ, HessEV et al.: Family study of fibromyalgia. Arthritis Rheum.50(3), 944–952 (2004).
  • Kato K , SullivanP, EvengardB, Pedersen NL: Importance of genetic influences on chronic widespread pain. Arthritis Rheum.54(5), 1682–1686 (2006).
  • Aaron LA , BuchwaldD: Fibromyalgia and other unexplained clinical conditions.Curr. Rheumatol. Rep.3(2), 116–122 (2001).
  • Hudson JI , MangwethB, PopeHG Jr et al.: Family study of affective spectrum disorder. Arch. Gen. Psychiatry60(2), 170–177 (2003).
  • Hudson JI , ArnoldL, KeckPE Jr, Auchenbach MB, Pope HG Jr: Family study of fibromyalgia and affective spectrum disorder. Biol. Psychiatry56(11), 884–891 (2004).
  • Walsh CM , ZainalN, MiddletonSJ, Paykel ES:A family history study of chronic fatigue syndrome. Psychiatr. Genet.11(3), 123–128 (2001).
  • Kalantar JS , Locke Gr, Zinsmeister AR, Beighley CM, Talley NJ: Familial aggregation of irritable bowel syndrome: a prospective study. Gut52(12), 1703–1707 (2003).
  • Bondy B , SpaethM, OffenbaecherM et al.: The T102C polymorphism of the 5-HT2A receptor gene in fibromyalgia. Neurobiol. Dis.6(5), 433–439 (1999).
  • Chen K , YangW, GrimsbyJ, ShihJC: The human 5-HT2 receptor is encoded by a multiple intron–exon gene.Brain Res. Molec. Brain Res.14(1–2), 20–26 (1992).
  • Ramamoorthy S , BaumanA, MooreKR et al.: Antidepressant- and cocaine-sensitive human serotonin transporter: molecular cloning, expression, and chromosomal localization. Proc. Natl Acad. Sci. USA90(6), 2542–2546 (1993).
  • Offenbaecher M , BondyB, de Jonge S et al.: Possible association of fibromyalgia with a polymorphism in the serotonin transporter gene regulatory region. Arthritis Rheum.42(11), 2482–2488 (1999).
  • Cohen H , BuskilaD, NeumannL, Ebstein RP: Confirmation of an association between fibromyalgia and serotonin transporter promoter region (5- HTTLPR) polymorphism, and relationship to anxiety-related personality traits. Arthritis Rheum.46(3), 845–847 (2002).
  • Gursoy S : Absence of association of the serotonin transporter gene polymorphism with the mentally healthy subset of fibromyalgia patients.Clin. Rheumatol.21(3), 194–197 (2002).
  • Shifman S , BronsteinM, SternfeldM et al.: A highly significant association between a COMT haplotype and schizophrenia. Am. J. Hum. Genet.71(6), 1296–1302 (2002).
  • Zubieta JK , HeitzegM, SmithYR et al.: COMT Val158Met genotype affects µ-opioid neurotransmitter responses to a pain stressor. Science299(5610), 1240–1243 (2003).
  • Gursoy S , ErdalE, HerkenH, MadenciE, AlasehirliB, ErdalN. Significance of catechol-O-methyltransferase gene polymorphism in fibromyalgia syndrome. Rheumatol. Int.23(3), 104–107 (2003).
  • Diatchenko L , SladeG, NackleyAG et al.: Genetic basis for individual variations in pain perception and the development of a chronic pain condition. Hum. Mol. Genet.14(1), 135–143 (2005).
  • Van Tol HH , WuC, GuanHC et al.: Multiple dopamine D4 receptor variants in the human population. Nature358(6382), 149–152 (1992).
  • Ebstein RP , NovickO, UmanskyR et al.: Dopamine D4 receptor (D4DR) exon III polymorphism associated with the human personality trait of novelty seeking. Nat. Genet.12(1), 78–80 (1996).
  • Buskila D , CohenH, NeumannL, Ebstein RP: An association between fibromyalgia and the dopamine D4 receptor exon III repeat polymorphism and relationship to novelty seeking personality traits. Mol. Psychiatry9(8), 730–731 (2004).
  • Narita M , NishigamiN, NaritaN et al.: Association between serotonin transporter gene polymorphism and chronic fatigue syndrome. Biochem. Biophys. Res. Commun.14(311), 264–266 (2003).
  • Heils A , TeufelA, PetriS et al.: Allelic variation of human serotonin transporter gene expression. J. Neurochem.66(6), 2621–2624 (1996).
  • Yeo A , BoydP, LumsdenS et al.: Association between a functional polymorphism in the serotonin transporter gene and diarrhoea predominant irritable bowel syndrome in women. Gut53(10), 1452–1458 (2004).
  • Pata C , ErdalE, YazcK, CamdevirenH, OzkayaM, UluO: Association of the -1438 G/A and 102 T/C polymorphism of the 5-HT2A receptor gene with irritable bowel syndrome 5-HT2A gene polymorphism in irritable bowel syndrome.J. Clin. Gastroenterol.38(7), 561–566 (2004).
  • Kim HJ , CamilleriM, CarlsonPJ et al.: Association of distinct α2 adrenoceptor and serotonin transporter polymorphisms with constipation and somatic symptoms in functional gastrointestinal disorders. Gut53(6), 829–837 (2004).
  • Mutlu N , ErdalM, HerkenH, OzG, BayazitYA: T102C polymorphism of the 5-HT2A receptor gene may be associated with temporomandibular dysfunction.Oral Dis.10(6), 349–352 (2004).
  • Juhasz G , ZesombokT, LaszikA et al.: Association analysis of 5-HTTLPR variants, 5-HT2A receptor gene 102T/C polymorphism and migraine. J. Neurogenet.17(2–3), 231–240 (2003).
  • Borroni B , BrambillaC, LiberiniP et al.: Functional serotonin 5-HTTLPR polymorphism is a risk factor for migraine with aura. J. Headache Pain6(4), 182–184 (2005).
  • Lee HJ , LeeM, KangRH et al.: Influence of the serotonin transporter promoter gene polymorphism on susceptibility to posttraumatic stress disorder. Depress. Anxiet.21(3), 135–139 (2005).
  • Frank B , NieslerB, BondyB et al.: Mutational analysis of serotonin receptor genes: HTR3A and HTR3B in fibromyalgia patients. Clin. Rheumatol.23(4), 338–344 (2004).

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