Each standard deviation increase in skin intrinsic fluorescence was associated with a 2.6-fold greater likelihood of autonomic neuropathy (P=0.006) and a 2.70-fold greater odds of CDSP (P=0.005).
Observational (n=111)
Is skin intrinsic fluorescence associated with autonomic and distal symmetrical polyneuropathy in individuals with type 1 diabetes?
Skin intrinsic fluorescence is strongly associated with both autonomic and distal symmetrical polyneuropathy in type 1 diabetes, outperforming mean HbA1c as a marker.
Odds Ratio: 2.6
p-value: p=0.006
OBJECTIVE: To determine whether skin intrinsic fluorescence (SIF) was associated with autonomic neuropathy and confirmed distal symmetrical polyneuropathy (CDSP) in 111 individuals with type 1 diabetes (mean age 49 years, mean diabetes duration 40 years). RESEARCH DESIGN AND METHODS: SIF was measured using the SCOUT DM device. Autonomic neuropathy was defined as an electrocardiographic abnormal heart rate response to deep breathing (expiration-to-inspiration ratio <1.1). CDSP was defined using the Diabetes Control and Complications Trial clinical exam protocol (the presence of two or more of the following: symptoms, sensory and/or motor signs, and/or reduced/absent tendon reflexes consistent with DSP) confirmed by the presence of an abnormal age-specific vibratory threshold (using a Vibratron II tester). RESULTS: The prevalence of autonomic neuropathy and CDSP were 61 and 66%, respectively. SIF was higher in those with autonomic neuropathy (P < 0.0001). In multivariable analyses controlling for age and updated mean (18-year average) HbA(1c), and allowing for other univariately and clinically significant correlates of autonomic neuropathy, each SD change in SIF was associated with a 2.6-greater likelihood of autonomic neuropathy (P = 0.006). Receiver operating characteristic (ROC) analyses revealed that SIF and updated mean HbA(1c) accounted for 80 and 57%, respectively, of the area under the curve (AUC) for autonomic neuropathy. SIF also was higher in those with CDSP (P < 0.0001) and remained so in multivariable analyses (odds ratio 2.70; P = 0.005). ROC analyses revealed that SIF and updated mean HbA(1c) accounted for 78 and 59%, respectively, of the AUC for CDSP. CONCLUSIONS: SIF, a marker of dermal advanced glycation end products, appears to be more strongly associated with the presence of both CDSP and autonomic neuropathy than mean HbA(1c).
Conway et al. (Thu,) conducted a observational in Type 1 diabetes (n=111). Skin intrinsic fluorescence (SIF) vs. Lower SIF was evaluated on Autonomic neuropathy (OR 2.6, p=0.006). Each standard deviation increase in skin intrinsic fluorescence was associated with a 2.6-fold greater likelihood of autonomic neuropathy (P=0.006) and a 2.70-fold greater odds of CDSP (P=0.005).
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