Nathan Efron

Prof. Nathan Efron

orcid

Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 July 2017 in The Ocular Surface
Verified
Journal Article
Closed access
JGJosé Alvaro P. Gomes
José Alvaro P. Gomes
DADimitri T. Azar
Dimitri T. Azar
CBChristophe Baudouin
Christophe Baudouin
NENathan Efron
Nathan Efron
MHMasatoshi Hirayama
Masatoshi Hirayama
James S. WolffsohnJames S. Wolffsohn
James S. Wolffsohn

8 January 2015 in Diabetes Care
Verified
Journal Article
Open access
PDF file
NPNicola Pritchard
Nicola Pritchard
KEKatie Edwards
Katie Edwards
ARAnthony W. Russell
Anthony W. Russell
BPBruce A. Perkins
Bruce A. Perkins
RMRAYAZ MALIK
RAYAZ MALIK
NENathan Efron
Nathan Efron
OBJECTIVE: This study determined if deficits in corneal nerve fiber length (CNFL) assessed using corneal confocal microscopy (CCM) can predict future onset of diabetic peripheral neuropathy (DPN). RESEARCH DESIGN AND METHODS: CNFL and a range of other baseline measures were compared between 90 nonneuropathic patients with type 1 diabetes who did or did not develop DPN after 4 years. The receiver operator characteristic (ROC) curve was used to determine the capability of single and combined measures of neuropathy to predict DPN. RESULTS: DPN developed in 16 participants (18%) after 4 years. Factors predictive of 4-year incident DPN were lower CNFL (P = 0.041); longer duration of diabetes (P = 0.002); higher triglycerides (P = 0.023); retinopathy (higher on the Early Treatment of Diabetic Retinopathy Study scale) (P = 0.008); nephropathy (higher albumin-to-creatinine ratio) (P = 0.001); higher neuropathy disability score (P = 0.037); lower cold sensation (P = 0.001) and cold pain (P = 0.027) thresholds; higher warm sensation (P = 0.008), warm pain (P = 0.024), and vibration (P = 0.003) thresholds; impaired monofilament response (P = 0.003); and slower peroneal (P = 0.013) and sural (P = 0.002) nerve conduction velocity. CCM could predict the 4-year incident DPN with 63% sensitivity and 74% specificity for a CNFL threshold cutoff of 14.1 mm/mm2 (area under ROC curve = 0.66, P = 0.041). Combining neuropathy measures did not improve predictive capability. CONCLUSIONS: DPN can be predicted by various demographic, metabolic, and conventional neuropathy measures. The ability of CCM to predict DPN broadens the already impressive diagnostic capabilities of this novel ophthalmic marker.

1 July 2007 in Progress in Retinal and Eye Research
Verified
Journal Article
Closed access
NENathan Efron
Nathan Efron

1 April 2007 in Optometry and Vision Science
Verified
Journal Article
Closed access
NENathan Efron
Nathan Efron
PMPhilip Morgan
Philip Morgan
ICIan D. Bsc(Hons) Cameron
Ian D. Bsc(Hons) Cameron
NBNOEL A. PhD BRENNAN
NOEL A. PhD BRENNAN
MGMarie Bsc(Hons) Goodwin
Marie Bsc(Hons) Goodwin

1 July 2016 in Progress in Retinal and Eye Research
Verified
Journal Article
Closed access
NENathan Efron
Nathan Efron
NBNoel A. Brennan
Noel A. Brennan
PMPhilip Morgan
Philip Morgan
TWTawnya Wilson
Tawnya Wilson

1 January 2008 in Clinical and Experimental Optometry
Verified
Journal Article
Closed access
PDF file
NENathan Efron
Nathan Efron
JHJoanna G Hollingsworth
Joanna G Hollingsworth