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  • Association between a stromal cell-derived factor 1 (SDF-1/CXCL12) gene polymorphism and microvascular disease in systemic sclerosis

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Clinical and epidemiological research
Association between a stromal cell-derived factor 1 (SDF-1/CXCL12) gene polymorphism and microvascular disease in systemic sclerosis
  1. M Manetti1,2,
  2. V Liakouli3,
  3. C Fatini4,
  4. P Cipriani3,
  5. C Bonino5,
  6. S Vettori6,
  7. S Guiducci2,
  8. C Montecucco5,
  9. R Abbate4,
  10. G Valentini6,
  11. M Matucci-Cerinic2,
  12. R Giacomelli3,
  13. L Ibba-Manneschi1
  1. 1
    Department of Anatomy, Histology and Forensic Medicine, University of Florence, Florence, Italy
  2. 2
    Department of Biomedicine, Division of Rheumatology, AOUC and Excellence Centre for Research, Transfer and High Education DENOthe, University of Florence, Florence, Italy
  3. 3
    Department of Internal Medicine and Public Health, Division of Rheumatology, University of L’Aquila, L’Aquila, Italy
  4. 4
    Department of Medical and Surgical Critical Care, Thrombosis Centre, University of Florence, Florence, Italy
  5. 5
    Division of Rheumatology, University of Pavia, IRCCS Policlinico S Matteo, Pavia, Italy
  6. 6
    Division of Rheumatology, II University of Naples, Naples, Italy
  1. Professor L Ibba-Manneschi, Department of Anatomy, Histology and Forensic Medicine, University of Florence, Viale G B Morgagni 85, 50134 Florence, Italy; ibba{at}unifi.it

Abstract

Objective: To investigate the possible implication of SDF1-3′ polymorphism in systemic sclerosis (SSc) susceptibility or clinical phenotype, or both.

Methods: 150 patients with SSc and 150 controls were enrolled. Skin involvement, autoantibodies, interstitial lung disease, pulmonary arterial hypertension (PAH), scleroderma renal crisis, past and/or current skin ulcers were assessed. Genotyping was performed by PCR-RFLP.

Results: Genotype distribution and allele frequency were similar in SSc and controls. SDF1-3′A allele and SDF1-3′GA/AA genotype frequencies were significantly higher in SSc-PAH than in SSc-non-PAH (33.3% vs 18.3%, p = 0.01) and in SSc with skin ulcers than in SSc without ulcers (27.3% vs 16.9%, p = 0.03). The SDF1-3′A allele influenced the predisposition to SSc-related PAH (OR = 2.52, 95% CI 1.11 to 5.69, p = 0.02) and skin ulcers (OR = 2.31, 95% CI 1.18 to 4.52, p = 0.01). After adjustment for age and gender, the SDF1-3′A allele remained a susceptibility factor for the SSc-related vascular manifestations (PAH: OR = 2.37, 95% CI 1.04 to 5.42, p = 0.04; ulcers: OR = 2.33, 95% CI 1.78 to 4.62, p = 0.01).

Conclusion: The SDF1-3′A allele is significantly associated with microvascular involvement in SSc.

https://doi.org/10.1136/ard.2008.098277

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    Footnotes

    • Competing interests: None.

    • Funding: This study has been supported by grants from the Ministero Italiano dell’Università e della Ricerca (MIUR) and the Associazione per lo studio della Sclerosi Sistemica e delle Malattie Fibrosanti (ASSMaF onlus).

    • Ethics approval: Approved by the local ethics committees.