Journal of the Neurological Sciences
Volume 290, Issue 1 , Pages 115-122, 15 March 2010

Differential gene expression in chronic inflammatory demyelinating polyneuropathy (CIDP) skin biopsies

  • Grace Lee

      Affiliations

    • Department of Neurology and Neuroscience, Weill Medical College of Cornell University, 525 E. 68th St, New York City, NY 10021, USA
    • Corresponding Author InformationCorresponding author.
  • ,
  • Zhaoying Xiang

      Affiliations

    • Department of Microbiology and Immunology, Weill Medical College of Cornell University, 525 E. 68th St, New York City, NY 10021, USA
  • ,
  • Thomas H. Brannagan III

      Affiliations

    • Neurological Institute, Columbia Presbyterian Medical Center, 710W 168 St, New York City, NY 10021, USA
  • ,
  • Russell L. Chin

      Affiliations

    • Department of Neurology and Neuroscience, Weill Medical College of Cornell University, 525 E. 68th St, New York City, NY 10021, USA
  • ,
  • Norman Latov

      Affiliations

    • Department of Neurology and Neuroscience, Weill Medical College of Cornell University, 525 E. 68th St, New York City, NY 10021, USA

Received 3 July 2009; received in revised form 14 September 2009; accepted 7 October 2009. published online 18 November 2009.

Abstract 

Gene expression analysis previously identified molecular markers that are up-regulated in sural nerve biopsies from patients with chronic inflammatory demyelinating polyneuropathy (CIDP). To determine whether the same or additional genes are also up-regulated in skin, we applied gene microarray profiling and quantitative real-time PCR (qPCR) analysis to skin punch biopsies from patients with CIDP and controls. Five genes, allograft inflammatory factor 1 (AIF-1), lymphatic hyaluronan receptor (LYVE-1/XLKD1), FYN binding protein (FYB), P2RY1 (purinergic receptor P2Y, G-protein-coupled, 1), and MLLT3 (myeloid/lymphoid or mixed-lineage leukemia translocated to, 3), all associated with immune cells or inflammatory processes, were elevated in punch skin biopsies from patients with CIDP as compared to normal subjects or patients with Charcot–Marie–Tooth Type 1 (CMT1). The average fold change of the 5 genes over normal expression, as determined by qPCR, was significantly elevated in skin biopsies from patients with CIDP in comparison to CMT1 or diabetic neuropathy, and similar to that seen in Lyme disease. The findings indicate the presence of inflammatory changes in the skin of patients with CIDP.

Keywords: Chronic inflammatory demyelinating polyneuropathy, CIDP, Differential gene expression, Skin, Diabetic neuropathy, Charcot–Marie–Tooth disease, CMT-1

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PII: S0022-510X(09)00902-2

doi:10.1016/j.jns.2009.10.006

Journal of the Neurological Sciences
Volume 290, Issue 1 , Pages 115-122, 15 March 2010