Corneal confocal microscopy: a non-invasive surrogate of nerve fibre damage and repair in diabetic patients

被引:386
作者
Malik, RA
Kallinikos, P
Abbott, CA
van Schie, CHM
Morgan, P
Efron, N
Boulton, AJM
机构
[1] Manchester Royal Infirm, Dept Med, Manchester M13 9WL, Lancs, England
[2] Univ Manchester, Inst Sci & Technol, Dept Optometry & Neurosci, Manchester M60 1QD, Lancs, England
关键词
diabetic neuropathy; confocal microscope; corneal nerves; surrogate; degeneration; regeneration;
D O I
10.1007/s00125-003-1086-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims/hypothesis. The accurate detection, characterization and quantification of human diabetic neuropathy are important to define at risk patients, anticipate deterioration, and assess new therapies. Corneal confocal microscopy is a reiterative, rapid, non-invasive in vivo clinical examination technique capable of imaging corneal nerve fibres. The aim of this study was to define the ability of this technique to quantify the extent of degeneration and regeneration of corneal nerve fibres in diabetic patients with increasing neuropathic severity. Methods. We scanned the cornea and collected images of Bowman's layer (containing a rich nerve plexus) from 18 diabetic patients and 18 age-matched control subjects. Results. Corneal nerve fibre density (F-3=9.6, p<0.0001), length (F-3=23.8, p<0.0001), and branch density (F-3=13.9, p<0.0001) were reduced in diabetic patients compared with control subjects, with a tendency for greater reduction in these measures with increasing severity of neuropathy. Conclusion/Interpretation. Corneal confocal microscopy is a rapid, non-invasive in vivo clinical examination technique which accurately defines the extent of corneal nerve damage and repair and acts as a surrogate measure of somatic neuropathy in diabetic patients. It could represent an advance to define the severity of neuropathy and expedite assessment of therapeutic efficacy in clinical trials of human diabetic neuropathy.
引用
收藏
页码:683 / 688
页数:6
相关论文
共 36 条
[1]   The North-West Diabetes Foot Care Study: incidence of, and risk factors for, new diabetic foot ulceration in a community-based patient cohort [J].
Abbott, CA ;
Carrington, AL ;
Ashe, H ;
Bath, S ;
Every, LC ;
Griffiths, J ;
Hann, AW ;
Hussein, A ;
Jackson, N ;
Johnson, KE ;
Ryder, CH ;
Torkington, R ;
Van Ross, ERE ;
Whalley, AM ;
Widdows, P ;
Williamson, S ;
Boulton, AJM .
DIABETIC MEDICINE, 2002, 19 (05) :377-384
[2]   Efficacy and safety of recombinant human nerve growth factor in patients with diabetic polyneuropathy - A randomized controled trial [J].
Apfel, SC ;
Schwartz, S ;
Adornato, BT ;
Freeman, R ;
Biton, V ;
Rendell, M ;
Vinik, A ;
Giuliani, M ;
Stevens, JC ;
Barbano, R ;
Dyck, PJ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2000, 284 (17) :2215-2221
[3]  
AREZZO JC, 1999, AM J MED, V30, pS9
[4]   SENSORY DENERVATION OF THE RABBIT CORNEA AFFECTS EPITHELIAL PROPERTIES [J].
BEUERMAN, RW ;
SCHIMMELPFENNIG, B .
EXPERIMENTAL NEUROLOGY, 1980, 69 (01) :196-201
[5]   Diabetic neuropathy [J].
Boulton, AJM ;
Malik, RA .
MEDICAL CLINICS OF NORTH AMERICA, 1998, 82 (04) :909-+
[6]   HEREDITARY SENSORY NEUROPATHY WITH NEUROTROPHIC KERATITIS - DESCRIPTION OF AN AUTOSOMAL RECESSIVE DISORDER WITH A SELECTIVE REDUCTION OF SMALL MYELINATED NERVE-FIBERS AND A DISCUSSION OF THE CLASSIFICATION OF THE HEREDITARY SENSORY NEUROPATHIES [J].
DONAGHY, M ;
HAKIN, RN ;
BAMFORD, JM ;
GARNER, A ;
KIRKBY, GR ;
NOBLE, BA ;
TAZIRMELBOUCY, M ;
KING, RHM ;
THOMAS, PK .
BRAIN, 1987, 110 :563-583
[7]   A standard test of heat-pain responses using CASE IV [J].
Dyck, PJ ;
Zimmerman, IR ;
Johnson, DM ;
Gillen, D ;
Hokanson, JL ;
Karnes, JL ;
Gruener, G ;
OBrien, PC .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1996, 136 (1-2) :54-63
[8]  
Dyck PJ, 2001, MUSCLE NERVE, V24, P307, DOI 10.1002/1097-4598(200103)24:3<307::AID-MUS1000>3.3.CO
[9]  
2-1
[10]   Laser-assisted in situ keratomileusis complications in diabetes mellitus [J].
Fraunfelder, FW ;
Rich, LF .
CORNEA, 2002, 21 (03) :246-248