Microcirculation abnormalities in patients with fibromyalgia – measured by capillary microscopy and laser fluxmetry
This unblinded preliminary case-control study was done to demonstrate functional and structural changes in the microcirculation of patients with primary fibromyalgia (FM). We studied 10 women (54.0 ± 3.7 years of age) with FM diagnosed in accordance with the classification criteria of the American C...
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Published in | Arthritis research & therapy Vol. 7; no. 2; pp. R209 - R216 |
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Main Authors | , , , , , , |
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01.01.2005
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Abstract | This unblinded preliminary case-control study was done to demonstrate functional and structural changes in the microcirculation of patients with primary fibromyalgia (FM). We studied 10 women (54.0 ± 3.7 years of age) with FM diagnosed in accordance with the classification criteria of the American College of Rheumatology, and controls in three groups (n = 10 in each group) – age-matched women who were healthy or who had rheumatoid arthritis or systemic scleroderma (SSc). All 40 subjects were tested within a 5-week period by the same investigators, using two noninvasive methods, laser fluxmetry and capillary microscopy. The FM patients were compared with the healthy controls (negative controls) and with rheumatoid arthritis patients and SSc patients (positive controls). FM patients had fewer capillaries in the nail fold (P < 0.001) and significantly more capillary dilatations (P < 0.05) and irregular formations (P < 0.01) than the healthy controls. Interestingly, the peripheral blood flow in FM patients was much less (P < 0.001) than in healthy controls but did not differ from that of SSc patients (P = 0.73). The data suggest that functional disturbances of microcirculation are present in FM patients and that morphological abnormalities may also influence their microcirculation. |
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AbstractList | This unblinded preliminary case-control study was done to demonstrate functional and structural changes in the microcirculation of patients with primary fibromyalgia (FM). We studied 10 women (54.0 ± 3.7 years of age) with FM diagnosed in accordance with the classification criteria of the American College of Rheumatology, and controls in three groups (n = 10 in each group) – age-matched women who were healthy or who had rheumatoid arthritis or systemic scleroderma (SSc). All 40 subjects were tested within a 5-week period by the same investigators, using two noninvasive methods, laser fluxmetry and capillary microscopy. The FM patients were compared with the healthy controls (negative controls) and with rheumatoid arthritis patients and SSc patients (positive controls). FM patients had fewer capillaries in the nail fold (P < 0.001) and significantly more capillary dilatations (P < 0.05) and irregular formations (P < 0.01) than the healthy controls. Interestingly, the peripheral blood flow in FM patients was much less (P < 0.001) than in healthy controls but did not differ from that of SSc patients (P = 0.73). The data suggest that functional disturbances of microcirculation are present in FM patients and that morphological abnormalities may also influence their microcirculation. This unblinded preliminary case-control study was done to demonstrate functional and structural changes in the microcirculation of patients with primary fibromyalgia (FM). We studied 10 women (54.0 +/- 3.7 years of age) with FM diagnosed in accordance with the classification criteria of the American College of Rheumatology, and controls in three groups (n = 10 in each group) - age-matched women who were healthy or who had rheumatoid arthritis or systemic scleroderma (SSc). All 40 subjects were tested within a 5-week period by the same investigators, using two noninvasive methods, laser fluxmetry and capillary microscopy. The FM patients were compared with the healthy controls (negative controls) and with rheumatoid arthritis patients and SSc patients (positive controls). FM patients had fewer capillaries in the nail fold (P < 0.001) and significantly more capillary dilatations (P < 0.05) and irregular formations (P < 0.01) than the healthy controls. Interestingly, the peripheral blood flow in FM patients was much less (P < 0.001) than in healthy controls but did not differ from that of SSc patients (P = 0.73). The data suggest that functional disturbances of microcirculation are present in FM patients and that morphological abnormalities may also influence their microcirculation.This unblinded preliminary case-control study was done to demonstrate functional and structural changes in the microcirculation of patients with primary fibromyalgia (FM). We studied 10 women (54.0 +/- 3.7 years of age) with FM diagnosed in accordance with the classification criteria of the American College of Rheumatology, and controls in three groups (n = 10 in each group) - age-matched women who were healthy or who had rheumatoid arthritis or systemic scleroderma (SSc). All 40 subjects were tested within a 5-week period by the same investigators, using two noninvasive methods, laser fluxmetry and capillary microscopy. The FM patients were compared with the healthy controls (negative controls) and with rheumatoid arthritis patients and SSc patients (positive controls). FM patients had fewer capillaries in the nail fold (P < 0.001) and significantly more capillary dilatations (P < 0.05) and irregular formations (P < 0.01) than the healthy controls. Interestingly, the peripheral blood flow in FM patients was much less (P < 0.001) than in healthy controls but did not differ from that of SSc patients (P = 0.73). The data suggest that functional disturbances of microcirculation are present in FM patients and that morphological abnormalities may also influence their microcirculation. This unblinded preliminary case-control study was done to demonstrate functional and structural changes in the microcirculation of patients with primary fibromyalgia (FM). We studied 10 women (54.0 +/- 3.7 years of age) with FM diagnosed in accordance with the classification criteria of the American College of Rheumatology, and controls in three groups (n = 10 in each group) - age-matched women who were healthy or who had rheumatoid arthritis or systemic scleroderma (SSc). All 40 subjects were tested within a 5-week period by the same investigators, using two noninvasive methods, laser fluxmetry and capillary microscopy. The FM patients were compared with the healthy controls (negative controls) and with rheumatoid arthritis patients and SSc patients (positive controls). FM patients had fewer capillaries in the nail fold (P < 0.001) and significantly more capillary dilatations (P < 0.05) and irregular formations (P < 0.01) than the healthy controls. Interestingly, the peripheral blood flow in FM patients was much less (P < 0.001) than in healthy controls but did not differ from that of SSc patients (P = 0.73). The data suggest that functional disturbances of microcirculation are present in FM patients and that morphological abnormalities may also influence their microcirculation. |
ArticleNumber | R209 |
Author | Forster, Adrian Uebelhart, Daniel Koppensteiner, Renate Sprott, Haiko Morf, Susanne Franzeck, Ulrich K Amann-Vesti, Beatrice |
AuthorAffiliation | 1 Department of Rheumatology, Institute of Physical Medicine, University Hospital, Zurich, Switzerland 2 Department of Medicine, Division of Vascular Medicine (Angiology), University Hospital, Zurich, Switzerland 3 Center for Vascular Diseases, Zurich, Switzerland |
AuthorAffiliation_xml | – name: 2 Department of Medicine, Division of Vascular Medicine (Angiology), University Hospital, Zurich, Switzerland – name: 3 Center for Vascular Diseases, Zurich, Switzerland – name: 1 Department of Rheumatology, Institute of Physical Medicine, University Hospital, Zurich, Switzerland |
Author_xml | – sequence: 1 givenname: Susanne surname: Morf fullname: Morf, Susanne – sequence: 2 givenname: Beatrice surname: Amann-Vesti fullname: Amann-Vesti, Beatrice – sequence: 3 givenname: Adrian surname: Forster fullname: Forster, Adrian – sequence: 4 givenname: Ulrich K surname: Franzeck fullname: Franzeck, Ulrich K – sequence: 5 givenname: Renate surname: Koppensteiner fullname: Koppensteiner, Renate – sequence: 6 givenname: Daniel surname: Uebelhart fullname: Uebelhart, Daniel – sequence: 7 givenname: Haiko surname: Sprott fullname: Sprott, Haiko |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/15743467$$D View this record in MEDLINE/PubMed |
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References_xml | – start-page: 303 volume-title: Checkliste Rheumatologie year: 1991 ident: 1340_CR1 – volume: 146 start-page: 1541 year: 1986 ident: 1340_CR10 publication-title: Arch Intern Med doi: 10.1001/archinte.1986.00360200103017 – volume: 26 start-page: 2159 year: 1999 ident: 1340_CR9 publication-title: J Rheumatol – volume: 39 start-page: 917 year: 2000 ident: 1340_CR4 publication-title: Rheumatology doi: 10.1093/rheumatology/39.8.917 – volume: 117 start-page: 1889 year: 1992 ident: 1340_CR12 publication-title: Dtsch Med Wochenschr doi: 10.1055/s-2008-1062526 – start-page: 48 volume-title: Ann Rheum Dis year: 2002 ident: 1340_CR16 – volume: 130 start-page: 708 year: 1972 ident: 1340_CR5 publication-title: Arch Intern Med doi: 10.1001/archinte.1972.03650050036006 – start-page: 6 volume-title: VASA year: 2001 ident: 1340_CR17 – volume: 13 start-page: 83 year: 1995 ident: 1340_CR7 publication-title: Clin Exp Rheumatol – volume: 19 start-page: 8 year: 1990 ident: 1340_CR13 publication-title: VASA – volume: 32 start-page: 21 year: 1988 ident: 1340_CR2 publication-title: Pain doi: 10.1016/0304-3959(88)90019-X – volume: 7 start-page: 384 year: 1988 ident: 1340_CR3 publication-title: Clin Rheumatol doi: 10.1007/BF02239197 – volume: 10 start-page: 21 year: 1991 ident: 1340_CR6 publication-title: Int J Microcirc Clin Exp – volume: 23 start-page: 183 year: 1980 ident: 1340_CR14 publication-title: Arthritis Rheum doi: 10.1002/art.1780230208 – volume: 24 start-page: 34 year: 1995 ident: 1340_CR15 publication-title: Scand J Rheumatol doi: 10.3109/03009749509095152 – volume: 33 start-page: 160 year: 1990 ident: 1340_CR8 publication-title: Arthritis Rheum doi: 10.1002/art.1780330203 – volume: 25 start-page: 5 year: 1997 ident: 1340_CR11 publication-title: VASA – reference: 7774109 - Clin Exp Rheumatol. 1995 Jan-Feb;13(1):83-6 – reference: 1459018 - Dtsch Med Wochenschr. 1992 Dec 4;117(49):1889-97 – reference: 7863276 - Scand J Rheumatol. 1995;24(1):34-7 – reference: 5083413 - Arch Intern Med. 1972 Nov;130(5):708-14 – reference: 2019481 - Int J Microcirc Clin Exp. 1991 Feb;10(1):21-31 – reference: 2306288 - Arthritis Rheum. 1990 Feb;33(2):160-72 – reference: 10952750 - Rheumatology (Oxford). 2000 Aug;39(8):917-21 – reference: 9163237 - Vasa. 1997;26(1):5-10 – reference: 3229083 - Clin Rheumatol. 1988 Sep;7(3):384-8 – reference: 3729634 - Arch Intern Med. 1986 Aug;146(8):1541-5 – reference: 10529133 - J Rheumatol. 1999 Oct;26(10):2159-67 – reference: 7362667 - Arthritis Rheum. 1980 Feb;23(2):183-9 – reference: 2448729 - Pain. 1988 Jan;32(1):21-6 – reference: 2188459 - Vasa. 1990;19(1):8-15 |
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SubjectTerms | Arm - blood supply Arthritis, Rheumatoid - physiopathology Capillaries - physiopathology Capillaries - ultrastructure Female Fibromyalgia - physiopathology Fingers - blood supply Humans Hyperemia - physiopathology Laser-Doppler Flowmetry Microcirculation Microscopy Middle Aged Nails - blood supply Scleroderma, Systemic - physiopathology Skin - blood supply Vasoconstriction |
Title | Microcirculation abnormalities in patients with fibromyalgia – measured by capillary microscopy and laser fluxmetry |
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