Increased Axonal Regeneration and Swellings in Intraepidermal Nerve Fibers Characterize Painful Phenotypes of Diabetic Neuropathy
Abstract We examined changes in intraepidermal nerve fibers (IENFs) to differentiate patients with diabetic neuropathy (DN) and diabetic neuropathic pain (DN-P) from those with DN without pain (DN-NOP). Punch skin biopsies were collected from the proximal thigh (PT) and distal leg (DL) of normal sub...
Saved in:
Published in | The journal of pain Vol. 14; no. 9; pp. 941 - 947 |
---|---|
Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
01.09.2013
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Abstract We examined changes in intraepidermal nerve fibers (IENFs) to differentiate patients with diabetic neuropathy (DN) and diabetic neuropathic pain (DN-P) from those with DN without pain (DN-NOP). Punch skin biopsies were collected from the proximal thigh (PT) and distal leg (DL) of normal subjects, patients with type 2 diabetes without evidence of DN (DM), or DN-P and DN-NOP patients. Protein gene product 9.5-positive (PGP+) immunohistochemistry was used to quantify total IENF, and growth-associated protein 43 (GAP43) for regenerating IENF. Compared to normal subjects and patients with type 2 diabetes without evidence of DN, both DN-P and DN-NOP have reduced PGP+ IENF densities in DL and PT. Although GAP43+ IENF densities were also reduced in DL for both DN-P and DN-NOP, the GAP43+ IENF densities in PT of DN-P remained at the control levels. Higher GAP43/PGP ratios were detected in DN-P compared to DN-NOP in the DL and PT. In parallel, increased numbers of axonal swellings per PGP+ fiber (axonal swelling/PGP) were detected in DN-P compared to normal subjects, patients with type 2 diabetes without evidence of DN, and DN-NOP in the DL. These axonal swellings were positive for tropomyosin-receptor-kinase A and substance P, suggesting that they are associated with nociception. Perspective Among patients with DN, the ratios of GAP43/PGP and axonal swelling/PGP are likely to differentiate painful from painless phenotypes. |
---|---|
AbstractList | We examined changes in intraepidermal nerve fibers (IENFs) to differentiate patients with diabetic neuropathy (DN) and neuropathic pain (DN-P) from those with DN without pain (DN-NOP). Punch skin biopsies were collected from the proximal thigh (PT) and distal leg (DL) of normal subjects (NS), patients with type 2 diabetes without evidence of DN (DM), or DN-P and DN-NOP patients. Protein gene product 9.5 (PGP) immunohistochemistry was used to quantify total IENF, and growth associated protein 43 (GAP43) for regenerating IENF. Compared to NS and DM, both DN-P and DN-NOP have reduced PGP+ IENF densities in DL and PT. Although GAP43+ IENF densities were also reduced in DL for both DN-P and DN-NOP, the GAP43+ IENF densities in PT of DN-P remained at the control levels. Higher GAP43/PGP ratios were detected in DN-P compared to DN-NOP in the DL and PT. In parallel, increased numbers of axonal swellings per PGP+ fiber (axonal swelling/PGP) were detected in DN-P compared to NS, DM, and DN-NOP in the DL. These axonal swellings were positive for tropomyosin-receptor-kinase (Trk) A and substance P, suggesting that they are associated with nociception. Abstract We examined changes in intraepidermal nerve fibers (IENFs) to differentiate patients with diabetic neuropathy (DN) and diabetic neuropathic pain (DN-P) from those with DN without pain (DN-NOP). Punch skin biopsies were collected from the proximal thigh (PT) and distal leg (DL) of normal subjects, patients with type 2 diabetes without evidence of DN (DM), or DN-P and DN-NOP patients. Protein gene product 9.5-positive (PGP+) immunohistochemistry was used to quantify total IENF, and growth-associated protein 43 (GAP43) for regenerating IENF. Compared to normal subjects and patients with type 2 diabetes without evidence of DN, both DN-P and DN-NOP have reduced PGP+ IENF densities in DL and PT. Although GAP43+ IENF densities were also reduced in DL for both DN-P and DN-NOP, the GAP43+ IENF densities in PT of DN-P remained at the control levels. Higher GAP43/PGP ratios were detected in DN-P compared to DN-NOP in the DL and PT. In parallel, increased numbers of axonal swellings per PGP+ fiber (axonal swelling/PGP) were detected in DN-P compared to normal subjects, patients with type 2 diabetes without evidence of DN, and DN-NOP in the DL. These axonal swellings were positive for tropomyosin-receptor-kinase A and substance P, suggesting that they are associated with nociception. Perspective Among patients with DN, the ratios of GAP43/PGP and axonal swelling/PGP are likely to differentiate painful from painless phenotypes. We examined changes in intraepidermal nerve fibers (IENFs) to differentiate patients with diabetic neuropathy (DN) and diabetic neuropathic pain (DN-P) from those with DN without pain (DN-NOP). Punch skin biopsies were collected from the proximal thigh (PT) and distal leg (DL) of normal subjects, patients with type 2 diabetes without evidence of DN (DM), or DN-P and DN-NOP patients. Protein gene product 9.5-positive (PGP+) immunohistochemistry was used to quantify total IENF, and growth-associated protein 43 (GAP43) for regenerating IENF. Compared to normal subjects and patients with type 2 diabetes without evidence of DN, both DN-P and DN-NOP have reduced PGP+ IENF densities in DL and PT. Although GAP43+ IENF densities were also reduced in DL for both DN-P and DN-NOP, the GAP43+ IENF densities in PT of DN-P remained at the control levels. Higher GAP43/PGP ratios were detected in DN-P compared to DN-NOP in the DL and PT. In parallel, increased numbers of axonal swellings per PGP+ fiber (axonal swelling/PGP) were detected in DN-P compared to normal subjects, patients with type 2 diabetes without evidence of DN, and DN-NOP in the DL. These axonal swellings were positive for tropomyosin-receptor-kinase A and substance P, suggesting that they are associated with nociception. Among patients with DN, the ratios of GAP43/PGP and axonal swelling/PGP are likely to differentiate painful from painless phenotypes. We examined changes in intraepidermal nerve fibers (IENFs) to differentiate patients with diabetic neuropathy (DN) and diabetic neuropathic pain (DN-P) from those with DN without pain (DN-NOP). Punch skin biopsies were collected from the proximal thigh (PT) and distal leg (DL) of normal subjects, patients with type 2 diabetes without evidence of DN (DM), or DN-P and DN-NOP patients. Protein gene product 9.5-positive (PGP+) immunohistochemistry was used to quantify total IENF, and growth-associated protein 43 (GAP43) for regenerating IENF. Compared to normal subjects and patients with type 2 diabetes without evidence of DN, both DN-P and DN-NOP have reduced PGP+ IENF densities in DL and PT. Although GAP43+ IENF densities were also reduced in DL for both DN-P and DN-NOP, the GAP43+ IENF densities in PT of DN-P remained at the control levels. Higher GAP43/PGP ratios were detected in DN-P compared to DN-NOP in the DL and PT. In parallel, increased numbers of axonal swellings per PGP+ fiber (axonal swelling/PGP) were detected in DN-P compared to normal subjects, patients with type 2 diabetes without evidence of DN, and DN-NOP in the DL. These axonal swellings were positive for tropomyosin-receptor-kinase A and substance P, suggesting that they are associated with nociception.UNLABELLEDWe examined changes in intraepidermal nerve fibers (IENFs) to differentiate patients with diabetic neuropathy (DN) and diabetic neuropathic pain (DN-P) from those with DN without pain (DN-NOP). Punch skin biopsies were collected from the proximal thigh (PT) and distal leg (DL) of normal subjects, patients with type 2 diabetes without evidence of DN (DM), or DN-P and DN-NOP patients. Protein gene product 9.5-positive (PGP+) immunohistochemistry was used to quantify total IENF, and growth-associated protein 43 (GAP43) for regenerating IENF. Compared to normal subjects and patients with type 2 diabetes without evidence of DN, both DN-P and DN-NOP have reduced PGP+ IENF densities in DL and PT. Although GAP43+ IENF densities were also reduced in DL for both DN-P and DN-NOP, the GAP43+ IENF densities in PT of DN-P remained at the control levels. Higher GAP43/PGP ratios were detected in DN-P compared to DN-NOP in the DL and PT. In parallel, increased numbers of axonal swellings per PGP+ fiber (axonal swelling/PGP) were detected in DN-P compared to normal subjects, patients with type 2 diabetes without evidence of DN, and DN-NOP in the DL. These axonal swellings were positive for tropomyosin-receptor-kinase A and substance P, suggesting that they are associated with nociception.Among patients with DN, the ratios of GAP43/PGP and axonal swelling/PGP are likely to differentiate painful from painless phenotypes.PERSPECTIVEAmong patients with DN, the ratios of GAP43/PGP and axonal swelling/PGP are likely to differentiate painful from painless phenotypes. |
Author | Singleton, J.Robinson Smith, A.Gordon Dauch, Jacqueline R Yanik, Brandon M Feldman, Eva L Cheng, Hsinlin T Hsieh, Wilson Porzio, Michael T |
AuthorAffiliation | a Department of Neurology, University of Michigan Medical Center, Ann Arbor, Michigan, USA b Department of Neurology, University of Utah, Salt Lake City, Utah, USA c College of Literature, Science, and the Arts, University of Michigan, Ann Arbor, Michigan, USA |
AuthorAffiliation_xml | – name: a Department of Neurology, University of Michigan Medical Center, Ann Arbor, Michigan, USA – name: b Department of Neurology, University of Utah, Salt Lake City, Utah, USA – name: c College of Literature, Science, and the Arts, University of Michigan, Ann Arbor, Michigan, USA |
Author_xml | – sequence: 1 fullname: Cheng, Hsinlin T – sequence: 2 fullname: Dauch, Jacqueline R – sequence: 3 fullname: Porzio, Michael T – sequence: 4 fullname: Yanik, Brandon M – sequence: 5 fullname: Hsieh, Wilson – sequence: 6 fullname: Smith, A.Gordon – sequence: 7 fullname: Singleton, J.Robinson – sequence: 8 fullname: Feldman, Eva L |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23685187$$D View this record in MEDLINE/PubMed |
BookMark | eNqFUk1vEzEUXKEi-gG_AAn5yGXD83q_fKBSFShEqqCicLa83ufEYWNv7d1AuPHP8SYtgh5AsmRLnplnz8xpcmSdxSR5TmFGgZav1rN1L42dZUDZDOKC4lFyQousTus8r4725zItOMBxchrCGoDSoqqeJMcZK-uC1tVJ8nNhlUcZsCUX352VHfmES7To5WCcJdK25OYbdp2xy0CMJQs7eIm9adFvIvgD-i2SS9OgD2S-kl6qAb35geQ6Pk2PHbleoXXDrsdAnCZvjGxwMCoSR-96Oax2T5PHWnYBn93tZ8mXy7ef5-_Tq4_vFvOLq1QVNQwpBWiYrrSq8kJhwxrIWA2q4VpLQEl5nbeaY9lQ3TLIgVc855XGWgKrmkyzs-T8oNuPzQZbhdNPOtF7s5F-J5w04u8ba1Zi6baCcZ4XZRYFXt4JeHc7YhjExgQVvZEW3RgEzTNe5lmMIUJf_Dnr95B73yOAHwDKuxA8aqHMsLc8jjadoCCmjMVa7DMWU8YC4tqLswfce_l_s14fWBg93hr0IiiDVmFrPKpBtM78h3_-gK9iKYyS3VfcYVi70cf2RBdEyASIm6l7U_UoA-AUGPsFlSPZxQ |
CitedBy_id | crossref_primary_10_1002_mus_27080 crossref_primary_10_1016_j_jns_2015_05_044 crossref_primary_10_3389_fpain_2021_790524 crossref_primary_10_1002_cbin_11457 crossref_primary_10_4103_1673_5374_226404 crossref_primary_10_1007_s00702_020_02145_7 crossref_primary_10_1016_j_jpain_2017_02_429 crossref_primary_10_1186_s13075_015_0818_8 crossref_primary_10_1007_s00125_023_05945_0 crossref_primary_10_1038_srep41401 crossref_primary_10_17116_patol201577243_49 crossref_primary_10_1371_journal_pone_0277133 crossref_primary_10_1097_j_pain_0000000000002401 crossref_primary_10_1371_journal_pone_0276564 crossref_primary_10_1111_jdi_13544 crossref_primary_10_1097_j_pain_0000000000000465 crossref_primary_10_2174_0115733998253213231031050044 crossref_primary_10_1016_j_nbd_2016_10_002 crossref_primary_10_1007_s12264_022_01011_8 crossref_primary_10_1210_er_2018_00107 crossref_primary_10_1002_ejp_1259 crossref_primary_10_1089_ars_2022_0158 crossref_primary_10_1093_ptj_pzac104 crossref_primary_10_1016_j_brainres_2014_07_012 crossref_primary_10_3389_fpain_2024_1485420 crossref_primary_10_1002_acn3_119 crossref_primary_10_1097_j_pain_0000000000000491 crossref_primary_10_1073_pnas_1716470115 crossref_primary_10_1016_j_neurol_2014_10_008 crossref_primary_10_1016_j_lfs_2018_05_016 crossref_primary_10_2337_db16_1181 crossref_primary_10_1177_19322968241279553 crossref_primary_10_1038_s41598_022_08100_8 crossref_primary_10_1097_j_pain_0000000000001381 crossref_primary_10_1097_j_pain_0000000000003120 crossref_primary_10_3389_fendo_2017_00012 crossref_primary_10_1080_14728222_2017_1275569 crossref_primary_10_1016_S1474_4422_17_30329_0 crossref_primary_10_1210_jc_2019_01072 crossref_primary_10_1016_j_jns_2017_01_005 crossref_primary_10_1097_j_pain_0000000000000648 crossref_primary_10_2174_1573399817666210707112413 crossref_primary_10_1186_s13023_023_02666_w crossref_primary_10_3389_fpain_2021_731658 crossref_primary_10_1016_j_neulet_2020_134764 crossref_primary_10_1007_s00125_017_4438_5 crossref_primary_10_1021_acschemneuro_3c00010 crossref_primary_10_1002_dmrr_3361 crossref_primary_10_1002_14651858_CD014675 crossref_primary_10_1007_s00125_020_05352_9 crossref_primary_10_1097_j_pain_0000000000000367 crossref_primary_10_1016_j_ynpai_2018_07_002 crossref_primary_10_1016_j_diabres_2018_08_020 crossref_primary_10_1002_mus_24351 crossref_primary_10_1038_s41574_021_00496_z crossref_primary_10_1016_j_neulet_2023_137406 crossref_primary_10_1111_ene_14757 crossref_primary_10_3390_diagnostics11020165 crossref_primary_10_1371_journal_pone_0191614 crossref_primary_10_2337_db14_0492 crossref_primary_10_3389_fendo_2023_1136796 crossref_primary_10_1097_j_pain_0000000000001922 crossref_primary_10_1007_s00415_022_11035_9 crossref_primary_10_1038_s41598_020_60422_7 crossref_primary_10_1016_j_neuro_2018_12_006 crossref_primary_10_1016_j_nbd_2023_106293 crossref_primary_10_1186_s40478_020_01088_0 crossref_primary_10_4093_dmj_2020_0216 crossref_primary_10_1111_ner_12767 crossref_primary_10_1007_s11892_019_1150_5 crossref_primary_10_1097_WCO_0000000000000472 crossref_primary_10_2147_JPR_S467249 crossref_primary_10_1097_BRS_0000000000002299 crossref_primary_10_3389_fendo_2019_00929 crossref_primary_10_1002_mus_27379 crossref_primary_10_1016_j_expneurol_2023_114428 crossref_primary_10_1093_brain_awab079 crossref_primary_10_1097_j_pain_0000000000002054 crossref_primary_10_1080_14737175_2020_1794825 |
Cites_doi | 10.1089/152091501750219994 10.1212/WNL.48.3.708 10.1002/(SICI)1097-4598(199903)22:3<360::AID-MUS9>3.0.CO;2-J 10.1111/j.1365-2559.2008.03096.x 10.1111/1523-1747.ep12614465 10.1212/01.wnl.0000194314.86486.a2 10.2337/diab.39.8.898 10.1016/j.nbd.2011.08.011 10.1212/01.WNL.0000070781.92512.A4 10.1111/j.1529-8027.2008.00180.x 10.1111/j.1526-4637.2007.00347.x 10.1093/brain/awh180 10.2337/diacare.29.04.06.dc05-2180 10.1093/brain/106.4.791 10.1002/mus.10567 10.1097/01.ajp.0000169670.47653.fb 10.1016/S0301-0082(03)00034-0 10.1001/archneur.55.12.1513 10.1093/brain/awm199 10.1097/NEN.0b013e3181bef710 10.1016/S0014-4886(02)00017-1 |
ContentType | Journal Article |
Copyright | American Pain Society 2013 American Pain Society Copyright © 2013 American Pain Society. Published by Elsevier Inc. All rights reserved. |
Copyright_xml | – notice: American Pain Society – notice: 2013 American Pain Society – notice: Copyright © 2013 American Pain Society. Published by Elsevier Inc. All rights reserved. |
DBID | AAYXX CITATION CGR CUY CVF ECM EIF NPM 7X8 5PM |
DOI | 10.1016/j.jpain.2013.03.005 |
DatabaseName | CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed MEDLINE - Academic PubMed Central (Full Participant titles) |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) MEDLINE - Academic |
DatabaseTitleList | MEDLINE - Academic MEDLINE |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1528-8447 |
EndPage | 947 |
ExternalDocumentID | PMC3994562 23685187 10_1016_j_jpain_2013_03_005 S1526590013009103 1_s2_0_S1526590013009103 |
Genre | Research Support, Non-U.S. Gov't Journal Article Research Support, N.I.H., Extramural |
GrantInformation_xml | – fundername: Juvenile Diabetes Research Foundation Center for the Study of Complications in Diabetes – fundername: American Diabetes Association grantid: ADA08CR52 – fundername: National Institutes of Health grantid: UO1-DK60994; 1K08NS061039; R01DK064814; M01RR0064 – fundername: NINDS NIH HHS grantid: K08 NS061039 – fundername: NIDDK NIH HHS grantid: P30 DK020572 – fundername: NIDDK NIH HHS grantid: U01-DK60994 – fundername: NIDDK NIH HHS grantid: 5P60 DK20572 – fundername: NINDS NIH HHS grantid: 1K08NS061039 – fundername: NCRR NIH HHS grantid: M01RR0064 – fundername: NIDDK NIH HHS grantid: R01DK064814 |
GroupedDBID | --- --K --M .~1 0R~ 123 1B1 1RT 1~. 1~5 4.4 457 4G. 53G 5VS 7-5 71M 8P~ AABNK AACTN AAEDT AAEDW AAHBH AAIKJ AAKOC AALRI AAOAW AAQFI AAQQT AAQXK AAWTL AAXLA AAXUO ABBQC ABCQJ ABIVO ABJNI ABMAC ABMZM ABWVN ABXDB ACDAQ ACGFO ACGFS ACJTP ACRPL ADBBV ADEZE ADMUD ADNMO ADVLN AEKER AENEX AEVXI AFJKZ AFTJW AFXBA AGHFR AGUBO AGWIK AGYEJ AITUG AJOXV AJRQY AKRWK ALMA_UNASSIGNED_HOLDINGS AMFUW AMRAJ ANZVX ASPBG AVWKF AZFZN BLXMC CAG COF CS3 DU5 EBS EJD EO8 EO9 EP2 EP3 F5P FDB FEDTE FGOYB FIRID FNPLU G-Q GBLVA HVGLF HZ~ IHE J1W J5H K-O L7B M41 MO0 MOBAO N9A O-L O9- OAUVE OG. OS- OZT P-8 P-9 P2P PC. Q38 R2- RIG ROL RPZ SCC SDF SDG SEL SES SEW SSZ T5K UHS UNMZH UV1 ~G- AAYWO AAYXX ACVFH ADCNI AEUPX AFPUW AGCQF AGQPQ AIGII AKBMS AKYEP APXCP CITATION CGR CUY CVF ECM EIF NPM 7X8 5PM EFKBS |
ID | FETCH-LOGICAL-c580t-100b3f7fc745ceb3b02380cb9ffa0ea1984df9e6b1fd3040979497fe8a037b2f3 |
IEDL.DBID | .~1 |
ISSN | 1526-5900 1528-8447 |
IngestDate | Thu Aug 21 18:08:41 EDT 2025 Fri Jul 11 03:42:40 EDT 2025 Thu Apr 03 07:09:52 EDT 2025 Tue Jul 01 01:15:44 EDT 2025 Thu Apr 24 22:57:51 EDT 2025 Sun Apr 06 06:53:47 EDT 2025 Sun Feb 23 10:18:41 EST 2025 |
IsDoiOpenAccess | false |
IsOpenAccess | true |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 9 |
Keywords | peripheral neuropathy intraepidermal nerve fiber Diabetic pain |
Language | English |
License | Copyright © 2013 American Pain Society. Published by Elsevier Inc. All rights reserved. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c580t-100b3f7fc745ceb3b02380cb9ffa0ea1984df9e6b1fd3040979497fe8a037b2f3 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
OpenAccessLink | http://www.jpain.org/article/S1526590013009103/pdf |
PMID | 23685187 |
PQID | 1429642005 |
PQPubID | 23479 |
PageCount | 7 |
ParticipantIDs | pubmedcentral_primary_oai_pubmedcentral_nih_gov_3994562 proquest_miscellaneous_1429642005 pubmed_primary_23685187 crossref_citationtrail_10_1016_j_jpain_2013_03_005 crossref_primary_10_1016_j_jpain_2013_03_005 elsevier_sciencedirect_doi_10_1016_j_jpain_2013_03_005 elsevier_clinicalkeyesjournals_1_s2_0_S1526590013009103 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | 2013-09-01 |
PublicationDateYYYYMMDD | 2013-09-01 |
PublicationDate_xml | – month: 09 year: 2013 text: 2013-09-01 day: 01 |
PublicationDecade | 2010 |
PublicationPlace | United States |
PublicationPlace_xml | – name: United States |
PublicationTitle | The journal of pain |
PublicationTitleAlternate | J Pain |
PublicationYear | 2013 |
Publisher | Elsevier Inc |
Publisher_xml | – name: Elsevier Inc |
References | Herrmann, McDermott, Henderson, Chen, Akowuah, Schifitto (bib9) 2004; 29 Holland, Stocks, Hauer, Cornblath, Griffin, McArthur (bib10) 1997; 48 Polydefkis, Hauer, Griffin, McArthur (bib15) 2001; 3 Christianson, Riekhof, Wright (bib5) 2003; 179 Cheng, Dauch, Hayes, Hong, Feldman (bib3) 2009; 68 McArthur, Stocks, Hauer, Cornblath, Griffin (bib14) 1998; 55 Gibbons, Griffin, Polydefkis, Bonyhay, Brown, Hauer, McArthur (bib8) 2006; 66 Ebenezer, McArthur, Thomas, Murinson, Hauer, Polydefkis, Griffin (bib6) 2007; 130 Sorensen, Molyneaux, Yue (bib19) 2006; 22 Cheng, Callaghan, Dauch, Feldman (bib2) 2011 Shun, Chang, Wu, Hsieh, Lin, Lin, Tai, Hsieh (bib17) 2004; 127 Said, Slama, Selva (bib16) 1983; 106 Singleton, Bixby, Russell, Feldman, Peltier, Goldstein, Howard, Smith (bib18) 2008; 13 Kennedy, Nolano, Wendelschafer-Crabb, Johnson, Tamura (bib11) 1999; 22 Lauria, Lombardi, Camozzi, Devigili (bib12) 2009; 54 Sorensen, Molyneaux, Yue (bib20) 2006; 29 Yasuda, Terada, Maeda, Kogawa, Sanada, Haneda, Kashiwagi, Kikkawa (bib22) 2003; 69 Cheng, Dauch, Hayes, Yanik, Feldman (bib4) 2012; 45 Fantini, Johansson (bib7) 1992; 99 Britland, Young, Sharma, Clarke (bib1) 1990; 39 Lauria, Morbin, Lombardi, Borgna, Mazzoleni, Sghirlanzoni, Pareyson (bib13) 2003; 61 Veves, Backonja, Malik (bib21) 2008; 9 Cheng (10.1016/j.jpain.2013.03.005_bib2) 2011 Sorensen (10.1016/j.jpain.2013.03.005_bib19) 2006; 22 Polydefkis (10.1016/j.jpain.2013.03.005_bib15) 2001; 3 Yasuda (10.1016/j.jpain.2013.03.005_bib22) 2003; 69 Christianson (10.1016/j.jpain.2013.03.005_bib5) 2003; 179 McArthur (10.1016/j.jpain.2013.03.005_bib14) 1998; 55 Ebenezer (10.1016/j.jpain.2013.03.005_bib6) 2007; 130 Cheng (10.1016/j.jpain.2013.03.005_bib3) 2009; 68 Lauria (10.1016/j.jpain.2013.03.005_bib12) 2009; 54 Cheng (10.1016/j.jpain.2013.03.005_bib4) 2012; 45 Said (10.1016/j.jpain.2013.03.005_bib16) 1983; 106 Sorensen (10.1016/j.jpain.2013.03.005_bib20) 2006; 29 Holland (10.1016/j.jpain.2013.03.005_bib10) 1997; 48 Veves (10.1016/j.jpain.2013.03.005_bib21) 2008; 9 Fantini (10.1016/j.jpain.2013.03.005_bib7) 1992; 99 Gibbons (10.1016/j.jpain.2013.03.005_bib8) 2006; 66 Kennedy (10.1016/j.jpain.2013.03.005_bib11) 1999; 22 Britland (10.1016/j.jpain.2013.03.005_bib1) 1990; 39 Herrmann (10.1016/j.jpain.2013.03.005_bib9) 2004; 29 Lauria (10.1016/j.jpain.2013.03.005_bib13) 2003; 61 Shun (10.1016/j.jpain.2013.03.005_bib17) 2004; 127 Singleton (10.1016/j.jpain.2013.03.005_bib18) 2008; 13 |
References_xml | – start-page: 657 year: 2011 end-page: 678 ident: bib2 article-title: Cytoskeleton, axonal transport, and mechanisms of axonal neuropathy publication-title: Cytoskeleton of the Nervous System – volume: 13 start-page: 218 year: 2008 end-page: 227 ident: bib18 article-title: The Utah Early Neuropathy Scale: A sensitive clinical scale for early sensory predominant neuropathy publication-title: J Peripher Nerv Syst – volume: 22 start-page: 261 year: 2006 end-page: 265 ident: bib19 article-title: The level of small nerve fiber dysfunction does not predict pain in diabetic Neuropathy: A study using quantitative sensory testing publication-title: Clin J Pain – volume: 99 start-page: 734 year: 1992 end-page: 742 ident: bib7 article-title: Expression of growth-associated protein 43 and nerve growth factor receptor in human skin: A comparative immunohistochemical investigation publication-title: J Invest Dermatol – volume: 66 start-page: 256 year: 2006 end-page: 258 ident: bib8 article-title: The utility of skin biopsy for prediction of progression in suspected small fiber neuropathy publication-title: Neurology – volume: 48 start-page: 708 year: 1997 end-page: 711 ident: bib10 article-title: Intraepidermal nerve fiber density in patients with painful sensory neuropathy publication-title: Neurology – volume: 127 start-page: 1593 year: 2004 end-page: 1605 ident: bib17 article-title: Skin denervation in type 2 diabetes: Correlations with diabetic duration and functional impairments publication-title: Brain – volume: 29 start-page: 883 year: 2006 end-page: 887 ident: bib20 article-title: The relationship among pain, sensory loss, and small nerve fibers in diabetes publication-title: Diabetes Care – volume: 69 start-page: 229 year: 2003 end-page: 285 ident: bib22 article-title: Diabetic neuropathy and nerve regeneration publication-title: Prog Neurobiol – volume: 45 start-page: 280 year: 2012 end-page: 287 ident: bib4 article-title: Nerve growth factor/p38 signaling increases intraepidermal nerve fiber densities in painful neuropathy of type 2 diabetes publication-title: Neurobiol Dis – volume: 130 start-page: 2703 year: 2007 end-page: 2714 ident: bib6 article-title: Denervation of skin in neuropathies: The sequence of axonal and Schwann cell changes in skin biopsies publication-title: Brain – volume: 22 start-page: 360 year: 1999 end-page: 371 ident: bib11 article-title: A skin blister method to study epidermal nerves in peripheral nerve disease publication-title: Muscle Nerve – volume: 39 start-page: 898 year: 1990 end-page: 908 ident: bib1 article-title: Association of painful and painless diabetic polyneuropathy with different patterns of nerve fiber degeneration and regeneration publication-title: Diabetes – volume: 68 start-page: 1229 year: 2009 end-page: 1243 ident: bib3 article-title: Nerve growth factor mediates mechanical allodynia in a mouse model of type 2 diabetes publication-title: J Neuropathol Exp Neurol – volume: 9 start-page: 660 year: 2008 end-page: 674 ident: bib21 article-title: Painful diabetic neuropathy: Epidemiology, natural history, early diagnosis, and treatment options publication-title: Pain Med – volume: 55 start-page: 1513 year: 1998 end-page: 1520 ident: bib14 article-title: Epidermal nerve fiber density: Normative reference range and diagnostic efficiency publication-title: Arch Neurol – volume: 179 start-page: 188 year: 2003 end-page: 199 ident: bib5 article-title: Restorative effects of neurotrophin treatment on diabetes-induced cutaneous axon loss in mice publication-title: Exp Neurol – volume: 29 start-page: 420 year: 2004 end-page: 427 ident: bib9 article-title: Epidermal nerve fiber density, axonal swellings and QST as predictors of HIV distal sensory neuropathy publication-title: Muscle Nerve – volume: 54 start-page: 273 year: 2009 end-page: 285 ident: bib12 article-title: Skin biopsy for the diagnosis of peripheral neuropathy publication-title: Histopathology – volume: 3 start-page: 23 year: 2001 end-page: 28 ident: bib15 article-title: Skin biopsy as a tool to assess distal small fiber innervation in diabetic neuropathy publication-title: Diabetes Technol Ther – volume: 106 start-page: 791 year: 1983 end-page: 807 ident: bib16 article-title: Progressive centripetal degeneration of axons in small fibre diabetic polyneuropathy publication-title: Brain – volume: 61 start-page: 631 year: 2003 end-page: 636 ident: bib13 article-title: Axonal swellings predict the degeneration of epidermal nerve fibers in painful neuropathies publication-title: Neurology – volume: 3 start-page: 23 year: 2001 ident: 10.1016/j.jpain.2013.03.005_bib15 article-title: Skin biopsy as a tool to assess distal small fiber innervation in diabetic neuropathy publication-title: Diabetes Technol Ther doi: 10.1089/152091501750219994 – volume: 48 start-page: 708 year: 1997 ident: 10.1016/j.jpain.2013.03.005_bib10 article-title: Intraepidermal nerve fiber density in patients with painful sensory neuropathy publication-title: Neurology doi: 10.1212/WNL.48.3.708 – volume: 22 start-page: 360 year: 1999 ident: 10.1016/j.jpain.2013.03.005_bib11 article-title: A skin blister method to study epidermal nerves in peripheral nerve disease publication-title: Muscle Nerve doi: 10.1002/(SICI)1097-4598(199903)22:3<360::AID-MUS9>3.0.CO;2-J – volume: 54 start-page: 273 year: 2009 ident: 10.1016/j.jpain.2013.03.005_bib12 article-title: Skin biopsy for the diagnosis of peripheral neuropathy publication-title: Histopathology doi: 10.1111/j.1365-2559.2008.03096.x – volume: 99 start-page: 734 year: 1992 ident: 10.1016/j.jpain.2013.03.005_bib7 article-title: Expression of growth-associated protein 43 and nerve growth factor receptor in human skin: A comparative immunohistochemical investigation publication-title: J Invest Dermatol doi: 10.1111/1523-1747.ep12614465 – volume: 66 start-page: 256 year: 2006 ident: 10.1016/j.jpain.2013.03.005_bib8 article-title: The utility of skin biopsy for prediction of progression in suspected small fiber neuropathy publication-title: Neurology doi: 10.1212/01.wnl.0000194314.86486.a2 – volume: 39 start-page: 898 year: 1990 ident: 10.1016/j.jpain.2013.03.005_bib1 article-title: Association of painful and painless diabetic polyneuropathy with different patterns of nerve fiber degeneration and regeneration publication-title: Diabetes doi: 10.2337/diab.39.8.898 – volume: 45 start-page: 280 year: 2012 ident: 10.1016/j.jpain.2013.03.005_bib4 article-title: Nerve growth factor/p38 signaling increases intraepidermal nerve fiber densities in painful neuropathy of type 2 diabetes publication-title: Neurobiol Dis doi: 10.1016/j.nbd.2011.08.011 – volume: 61 start-page: 631 year: 2003 ident: 10.1016/j.jpain.2013.03.005_bib13 article-title: Axonal swellings predict the degeneration of epidermal nerve fibers in painful neuropathies publication-title: Neurology doi: 10.1212/01.WNL.0000070781.92512.A4 – volume: 13 start-page: 218 year: 2008 ident: 10.1016/j.jpain.2013.03.005_bib18 article-title: The Utah Early Neuropathy Scale: A sensitive clinical scale for early sensory predominant neuropathy publication-title: J Peripher Nerv Syst doi: 10.1111/j.1529-8027.2008.00180.x – volume: 9 start-page: 660 year: 2008 ident: 10.1016/j.jpain.2013.03.005_bib21 article-title: Painful diabetic neuropathy: Epidemiology, natural history, early diagnosis, and treatment options publication-title: Pain Med doi: 10.1111/j.1526-4637.2007.00347.x – volume: 127 start-page: 1593 year: 2004 ident: 10.1016/j.jpain.2013.03.005_bib17 article-title: Skin denervation in type 2 diabetes: Correlations with diabetic duration and functional impairments publication-title: Brain doi: 10.1093/brain/awh180 – volume: 29 start-page: 883 year: 2006 ident: 10.1016/j.jpain.2013.03.005_bib20 article-title: The relationship among pain, sensory loss, and small nerve fibers in diabetes publication-title: Diabetes Care doi: 10.2337/diacare.29.04.06.dc05-2180 – start-page: 657 year: 2011 ident: 10.1016/j.jpain.2013.03.005_bib2 article-title: Cytoskeleton, axonal transport, and mechanisms of axonal neuropathy – volume: 106 start-page: 791 issue: Pt 4 year: 1983 ident: 10.1016/j.jpain.2013.03.005_bib16 article-title: Progressive centripetal degeneration of axons in small fibre diabetic polyneuropathy publication-title: Brain doi: 10.1093/brain/106.4.791 – volume: 29 start-page: 420 year: 2004 ident: 10.1016/j.jpain.2013.03.005_bib9 article-title: Epidermal nerve fiber density, axonal swellings and QST as predictors of HIV distal sensory neuropathy publication-title: Muscle Nerve doi: 10.1002/mus.10567 – volume: 22 start-page: 261 year: 2006 ident: 10.1016/j.jpain.2013.03.005_bib19 article-title: The level of small nerve fiber dysfunction does not predict pain in diabetic Neuropathy: A study using quantitative sensory testing publication-title: Clin J Pain doi: 10.1097/01.ajp.0000169670.47653.fb – volume: 69 start-page: 229 year: 2003 ident: 10.1016/j.jpain.2013.03.005_bib22 article-title: Diabetic neuropathy and nerve regeneration publication-title: Prog Neurobiol doi: 10.1016/S0301-0082(03)00034-0 – volume: 55 start-page: 1513 year: 1998 ident: 10.1016/j.jpain.2013.03.005_bib14 article-title: Epidermal nerve fiber density: Normative reference range and diagnostic efficiency publication-title: Arch Neurol doi: 10.1001/archneur.55.12.1513 – volume: 130 start-page: 2703 year: 2007 ident: 10.1016/j.jpain.2013.03.005_bib6 article-title: Denervation of skin in neuropathies: The sequence of axonal and Schwann cell changes in skin biopsies publication-title: Brain doi: 10.1093/brain/awm199 – volume: 68 start-page: 1229 year: 2009 ident: 10.1016/j.jpain.2013.03.005_bib3 article-title: Nerve growth factor mediates mechanical allodynia in a mouse model of type 2 diabetes publication-title: J Neuropathol Exp Neurol doi: 10.1097/NEN.0b013e3181bef710 – volume: 179 start-page: 188 year: 2003 ident: 10.1016/j.jpain.2013.03.005_bib5 article-title: Restorative effects of neurotrophin treatment on diabetes-induced cutaneous axon loss in mice publication-title: Exp Neurol doi: 10.1016/S0014-4886(02)00017-1 |
SSID | ssj0011577 |
Score | 2.371809 |
Snippet | Abstract We examined changes in intraepidermal nerve fibers (IENFs) to differentiate patients with diabetic neuropathy (DN) and diabetic neuropathic pain... We examined changes in intraepidermal nerve fibers (IENFs) to differentiate patients with diabetic neuropathy (DN) and diabetic neuropathic pain (DN-P) from... We examined changes in intraepidermal nerve fibers (IENFs) to differentiate patients with diabetic neuropathy (DN) and neuropathic pain (DN-P) from those with... |
SourceID | pubmedcentral proquest pubmed crossref elsevier |
SourceType | Open Access Repository Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 941 |
SubjectTerms | Aged Anesthesia & Perioperative Care Axons - pathology Diabetic Neuropathies - complications Diabetic pain Epidermis - innervation Female GAP-43 Protein - metabolism Humans intraepidermal nerve fiber Male Middle Aged Nerve Degeneration Nerve Fibers - metabolism Nerve Fibers - pathology Neuralgia - etiology Pain Measurement Pain Medicine peripheral neuropathy Receptor, trkA - metabolism Substance P - metabolism TRPV Cation Channels - metabolism |
Title | Increased Axonal Regeneration and Swellings in Intraepidermal Nerve Fibers Characterize Painful Phenotypes of Diabetic Neuropathy |
URI | https://www.clinicalkey.es/playcontent/1-s2.0-S1526590013009103 https://dx.doi.org/10.1016/j.jpain.2013.03.005 https://www.ncbi.nlm.nih.gov/pubmed/23685187 https://www.proquest.com/docview/1429642005 https://pubmed.ncbi.nlm.nih.gov/PMC3994562 |
Volume | 14 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1La9wwEBYhh9BL6bubpkGFHuuubEuWfQxLlrSQEJoGchN6Ng6Ld6l3oe0h0H_eGflBtqE5FHyyx-g1mhlJn74h5H3BrQPrZ2GZavKE68IkpdEskVaKQotUC4sb-qdnxckl_3wlrnbIbLgLg7DK3vZ3Nj1a6_7NtO_N6aqupxcpMrtX8egNnR4yfnIuUcs_3o4wD-SSiQlWQDhB6YF5KGK8blaw_EZ8V94xnYp_eaf70effIMo7Xmn-hDzuw0l61NX4KdnxzTOyd9ofmD8nv2H-I-zcO3r0A4Nu-sV_i0zTOCBUN45e4PYd7pfTuqGfsBSPWWPBYC_oGeIh6RxRJS2djdzOvzw9hyaFzYKeX_tmifu4LV0G2uFraksj5wdmO_75glzOj7_OTpI-60JiRcnWYJeZyYMMVnJhYalt0Ksza6oQNPM6rUruQuULkwaXM6TLqnglgy81y6XJQv6S7DbLxr8m1DlhWcGsdtJwwwoN0QOTLtcgbqCwCcmG3la2pyTHzBgLNWDPblQcIoVDpBg8TEzIh_GnVcfI8bC4HIZRDZdNwTz6tp-rrUpVmymm7unThBTjn1sqqcDbPFzku0FdFExWPIHRjV9uoCiOp9xZlHnVqc_YhgxTAaSlhApvKdYogETg21-a-joSgkOQiQvZ_f-t8BvyKItZPhA6d0B21983_i3EWmtzGCfTH3g8KoY |
linkProvider | Elsevier |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwELZKkYAL4s3yNBJHwjqJHSfHasVqC91VRVupN8t2bJpqlV2RXQk4IPHPmXEeYqnoASmnZCK_xjNj-_M3hLzNuC3B-llYppo04jozUW40i6SVItMi1sLihv58kc3O-Mdzcb5HJv1dGIRVdra_tenBWndvxl1vjtdVNT6Jkdm9CEdv6PTSG-Qmh-mLaQze_xxwHkgmEzKsgHSE4j31UAB5Xa5h_Y0Ar7SlOhX_ck9Xw8-_UZR_uKXpPXK3iyfpQVvl-2TP1Q_IrXl3Yv6Q_AIDgLhzV9KDbxh108_uS6CaxhGhui7pCe7f4YY5rWp6iKU4TBsLFntJFwiIpFOElTR0MpA7_3D0GJrkt0t6fOHqFW7kNnTlaQuwqSwNpB-Y7vj7I3I2_XA6mUVd2oXIipxtwDAzk3rpreTCwlrboFtn1hTea-Z0XOS89IXLTOzLlCFfVsEL6V2uWSpN4tPHZL9e1e4poWUpLMuY1aU03LBMQ_jAZJlqEDdQ2IgkfW8r23GSY2qMperBZ5cqDJHCIVIMHiZG5N3w07ql5LheXPbDqPrbpmAfXdNN1kbFqkkUU1cUakSy4c8dnVTgbq4v8k2vLgpmKx7B6NqttlAUx2PuJMg8adVnaEOCuQDiXEKFdxRrEEAm8N0vdXURGMEhysSV7LP_rfBrcnt2Oj9SR4eLT8_JnSSk_EAc3Quyv_m6dS8h8NqYV2Fi_QZkDC2i |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Increased+axonal+regeneration+and+swellings+in+intraepidermal+nerve+fibers+characterize+painful+phenotypes+of+diabetic+neuropathy&rft.jtitle=The+journal+of+pain&rft.au=Cheng%2C+H.T.&rft.au=Dauch%2C+J.R.&rft.au=Porzio%2C+M.T.&rft.au=Yanik%2C+B.M.&rft.date=2013-09-01&rft.issn=1526-5900&rft.eissn=1528-8447&rft.volume=14&rft.issue=9&rft.spage=941&rft.epage=947&rft_id=info:doi/10.1016%2Fj.jpain.2013.03.005&rft_id=info%3Apmid%2F23685187&rft.externalDocID=PMC3994562 |
thumbnail_m | http://utb.summon.serialssolutions.com/2.0.0/image/custom?url=https%3A%2F%2Fcdn.clinicalkey.com%2Fck-thumbnails%2F15265900%2FS1526590013X00094%2Fcov150h.gif |