Effect of Strict Glucose Control on Development of Diabetic Neuropathy

Introduction
Diabetes has been primarily categorized as Type 1 Diabetes Mellitus (T1DM), which has
juvenile onset and Type 2 Diabetes Mellitus (T2DM), which develops in late life. Diabetic
neuropathy impacts one-tenth of the people with diabetes mellitus during diagnosis and around
40%-50% after 10 years of development. Diabetic neuropathy includes a wide array of clinical
and subclinical manifestations with varying anatomical distributions, clinical courses, and
potentially varying causal pathogenetic mechanisms. Development and advancement of diabetic
neuropathy is independently linked with duration of diabetes, glucose control, and prior
cardiovascular risk factors. The pathogenesis of diabetic neuropathy is still not clearly known
however; insulin resistance, oxidative stress, mitochondrial malfunction, impaired glucose
metabolism, advanced glycation end products, neurotrophic factors, and protein kinase C
activation may be the contributing factor. It is suggested that strict glycemic control is the single
available intervention to avoid or postpone the development of diabetic neuropathy among its
patients (Habib & Brannagan, 2010).
Objectives
This review is done with the aim of examining the effect of maintenance of strict glucose control
within normal physiological range on development of diabetic neuropathy among patients of
T1DM and T2DM.
Methodology
A review of the literature is performed. Different databases including PuBMed, CNAHIL,
ScienceDirect, etc. were searched for studies published between 2008 and 2018. Various short
and long keywords were used for search including “blood glucose”, “diabetic neuropathy”,
“strict control”, “Type 1 diabetes mellitus” and “Type-2 diabetes mellitus”. Boolean operators of
AND and OR were used to make the search more focused and productive. Studies that examine
the association between strict glycemic control and reported neuropathy outcomes were
considered. The primary outcome measure was occurrence of clinical neuropathy identified by a
clinical scale. Author screened the titles and abstracts of retrieved studies from the database for
inclusion in the review on the basis of relevance. Inclusion criteria included published within last
10 years, English language, availability of full-text format and relevance to the research topic.

Literature review
Neuropathy is considered as one of the most prevalent, diminishing and expensive complications
of diabetes. One of the studies identified that management of diabetic neuropathy must always
initiate with interventions for optimizing glucose control along with patient education. The study
also established the availability of the useful pharmacologic interventions for treatment of
neuropathy but disease modifying interventions apart from tight glucose control still need an
improved understanding of the causal mechanisms of diabetic neuropathy and the formation of
pharmacologic entities (Edwards, et al., 2008).
Another review was conducted to investigate the evidence for strict glucose control to prevent
distal symmetric polyneuropathy in patients of T1DM and T2DM. The review concluded that
strict glycemic control in T1DM substantially decreases the development of clinical neuropathy
after 1 year of intensive glucose control. However, for T2DM, decrease in development of
neuropathy after 1 year of intensive glucose control was small and not statistically significant.
The review also identified the presence of large amplified likelihhod of adverse events with
increased glycemic control in T1DM and T2DM. specifically, in T2DM, there was a
considerably massive increase in the likelihood of weight gain and a considerable boost in the
risk of death. Therefore, strict glucose control substantially increases the likelihood of adverse
hypoglycemic events, which must be considered at the time of examining its risk/benefit ratio
(Callaghan, et al., 2012).
Another study established that recent guidelines for management of T2DM are based on glucose
norms inferred through the epidemiological studies; but the disease course from prediabetic stage
to terminal complications, differs in every patient. Vascular complications which includes
neuropathy, are strongly linked with hemoglobin A1c (HbA1c). But the microvascular
complications can advance in people who have HbA1c less than 7.0% and even develop in
people who are not yet diagnosed because of the transient boost in plasma glucose amounts.
Comorbidities of atherosclerosis and occult macrovascular impairments can appear in
accelerated pathway in T2DM. Macrovascular complications usually exhibit an early
development and do not link linearly with HbA1c like microvascular complications.
Management of hyperglycemia in subsequent stages of T2DM may not be related to better
cardiovascular consequences. The glucotoxicity and lipotoxicity that may appear before the

extended hyperglycemia and beta-cell dysfunction are early, reversible pathophysiologic
activities. It indicates that hastened management can alter the pathway of hyperglycemia and
avoid or postpone complications in the long run. Difficulty of identifying people with early
T2DM who are at risk for prompt advancement of beta-cell reduction and premature
development of microvascular complications is still there. Continuing investigations of the
mechanisms which attribute to diabetic complications may give new markers to assist in
identification of people with T2DM who can gain advantage from initial antidiabetics
management (Stolar, 2010).
Glucose regulation is a changeable risk factor for diabetic neuropathy (Duckworth, et al., 2009),
and people with good to excellent glycemic regulation for 5 years’ experience a 60% to 70%
decrease in the prevalence of neuropathy compared with those who have poor management of
diabetes (Wick, 2012). Strict glycemic control lowers neuropathy in people with T1DM in a
better way than it does in people with T2DM. It is possibly because of the differences of the time
period of the neuropathic modifications prior to diabetes onset or diagnosis of T2DM usually
occurs after a long duration of obesity and metabolic disorder. The consequences of persistent
metabolic strike, including oxidative stress, inflammation, and cellular injury, which may not be
stopped or reversed. Strict glycemic control singly is an inadequate strategy for patients of
T2DM as they usually respond less strongly than people with T1DM. Another study examined
the association between blood glucose amount and the vascular complications rate among
patients of T2DM. It was found that strict control failed to lower the likelihood of advanced
measures of microvascular consequences, however, it postponed the start of albuminuria and
certain aspects of eye complications and neuropathy (Ismail-Beigi, et al., 2010).
T2DM with optimal HbA1c can have varying terms of glycemic flexibility and microvascular
complication outcomes. A study was conducted to examine the link between glycemic flexibility
and diabetic neuropathy in T2DM with optimal HbA1c, that is less than 7.0%. A direct link
between glycemic flexibility examined through diabetic neuropathy in T2DM with optimal
HbA1c was observed (Xu, et al., 2014).
It is not established in studies whether strict glucose control can reverse already existing
neuropathy, but, the earlier and more effectively the strict control is done, more effectively
neuropathy can be prevented in T1DM (Pop-Busui, et al., 2010) and, possibly, T2DM. More