Diabetic neuropathy
Peer reviewed by Dr Colin Tidy, MRCGPLast updated by Dr Hayley Willacy, FRCGP Last updated 21 Oct 2024
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Professional Reference articles are designed for health professionals to use. They are written by UK doctors and based on research evidence, UK and European Guidelines. You may find the Diabetic neuropathy article more useful, or one of our other health articles.
In this article:
See the separate Diabetic foot article. Diabetes may cause polyneuropathy, mononeuropathy, amyotrophy and autonomic neuropathy.
Continue reading below
What is diabetic neuropathy?
Diabetic neuropathy is nerve damage caused by diabetes. It is a common complication of both type 1 diabetes and type 2 diabetes.
Neuropathy plays a major role in the development of foot ulcers, which cause an enormous effect on quality of life for the patient (especially if amputation becomes necessary) and is also responsible for a very large health and social services expenditure.
Optimal control of all metabolic factors and regular organised surveillance of all people with diabetes are essential to reduce the risk of both development and progression of diabetic neuropathy and therefore reduce the risk of disability for the patient.
Motor, sensory and autonomic fibres may all be affected by diabetic neuropathy.
How common is diabetic neuropathy? (Epidemiology)
Distal symmetrical polyneuropathy (DSPN) is the most common diabetic peripheral neuropathy (DPN), affecting about 50% of patients with type 2 diabetes after 10 years and at least 20% of patients with type 1 diabetes after 20 years.1 DSPN may be present in approximately 20–25% of newly diagnosed patients with type 2 diabetes.
Risk factors
Smoking.
Age over 40 years.
History of periods of poor glycaemic control.
Prevalence increases with increased duration of diabetes.
People with signs of neuropathy are likely also to have evidence of diabetic nephropathy and diabetic retinopathy.
Hypertension.
Coronary heart disease.
Continue reading below
Symptoms of diabetic neuropathy (presentation)
The presentation depends on the type of neuropathy involved. 50% of people with diabetic polyneuropathy may have no symptoms and are only diagnosed by careful, regular and thorough clinical examination.2
Peripheral sensorimotor (chronic peripheral neuropathy)
Sensory nerves are affected more than motor.
Touch, pain and temperature sensation and proprioception in lower limbs in a glove and stocking distribution.
Loss of ankle jerks and, later, knee jerks.
Hands are only affected in severe long-standing neuropathy.
Equal prevalence in types 1 and 2.
Acute diffuse painful (acute peripheral neuritis)
Often abrupt onset and not related to duration of diabetes.
Can resolve completely.
Burning foot pain, often worse at night.
Associated with poor glycaemic control but sometimes initially follows establishing good glycaemic control.
Examination may be normal apart from hyperaesthesia.
Acute painful neuropathy of rapid improvement of blood glucose control3
Acute painful neuropathy resulting from rapid improvement of blood glucose control is a self-limiting condition that improves symptomatically over time.
Autonomic neuropathy
Risk factors include hypertension and dyslipidaemia. It is more common in females.
It may present with:
Cardiac autonomic neuropathy, which has been linked to:4
Resting tachycardia, postural hypotension, orthostatic bradycardia and orthostatic tachycardia.
Exercise intolerance.
Decreased hypoxia-induced respiratory drive.
Loss of baroreceptor sensitivity, increased intra-operative or peri-operative cardiovascular lability.
Increased incidence of asymptomatic myocardial ischaemia, myocardial infarction, decreased rate of survival after myocardial infarction.
Congestive heart failure.
Genitourinary symptoms:
Impotence, retrograde ejaculation, urinary hesitancy, overflow incontinence.
At least 25% of men with diabetes have problems with sexual function.
There is often no association with glycaemic control or with duration or severity of diabetes.
Risk factors for erectile dysfunction include increasing age, alcohol, initial glycaemic control, intermittent claudication and retinopathy.
Gastrointestinal symptoms:
Nausea and vomiting.
Abdominal distension.
Dysphagia.
Diarrhoea.
Gustatory sweating, anhidrosis.
Tends to be associated with peripheral neuropathy.
People with both types 1 and 2 are affected.
High mortality rate (50% within three years) mainly due to chronic kidney disease but there is often no obvious cause.
Tight glycaemic control reduces the risk.
Mononeuropathy
External pressure or entrapment - eg, carpal tunnel syndrome.
Isolated neuropathies of either the cranial or peripheral nerves. Mononeuropathies of cranial nerves III, IV and VI, intercostal nerves and femoral nerves are common.
Occasionally more than one nerve is involved (mononeuritis multiplex).
Proximal motor (diabetic amyotrophy)
Main motor manifestation.
Severe pain and paraesthesiae in the upper legs, with weakness and muscle wasting of the thigh and pelvic girdle muscles.
May be asymmetrical and there may be extensor plantars.
Mainly affects middle-aged and elderly patients.
Usually associated with a period of very poor glycaemic control, sometimes with dramatic weight loss.
Pain and weakness gradually reduce once good glycaemic control has returned.
Differential diagnosis
Other possible causes of neuropathy include:
Toxins (eg, alcohol, occupational, vitamin B6), medications (eg, amiodarone).
Malignancies, amyloidosis.
Collagen vascular disease, neurosarcoidosis.
Tabes dorsalis, AIDS.
Spinal cord disease, cauda equina syndrome.
Continue reading below
Diagnosing diabetic neuropathy (investigations)
Full assessment of diabetes and blood pressure control. Assessment of other possible causes - eg, TFTs, B12.
May require nerve conduction studies and electromyography.
Management of diabetic neuropathy5
Regular surveillance for signs of neuropathy to allow early intervention.
Tight glycaemic control.
Prevention of foot trauma.
Management of painful neuropathy
May require a great deal of support for the depressing and disabling nature of the condition.
General measures
Bed foot cradles for problems at night.
Simple analgesia taken in advance of diurnal symptoms.
Contact dressings.
Drug treatments recommended by the National Institute for Health and Care Excellence (NICE)5
Offer a choice of amitriptyline, duloxetine, gabapentin or pregabalin as initial treatment for neuropathic pain. Note that as of April 2019, gabapentin and pregabalin became scheduled as Class C controlled substances (under the Misuse of Drugs Act 1971) and Schedule 3 under the Misuse of Drugs Regulations 2001. Before prescribing, patients should be evaluated for a history of drug abuse and observed for signs of abuse and dependence.
If the initial treatment is not effective or is not tolerated, offer one of the remaining three drugs; consider switching again if the second and third drugs tried are also not effective or not tolerated.
Consider tramadol only if acute rescue therapy is needed.
Consider capsaicin cream for people with localised neuropathic pain who wish to avoid, or who cannot tolerate, oral treatments.
Opioids other than tramadol should be avoided unless they are part of shared-care arrangements after specialist assessment.
Patients on drug treatment should be reviewed early when starting treatment for dosage titration, or when changing dose to monitor for adverse effects and tolerability.
Regular reviews (NICE does not specify a time interval) should also be arranged to check progress, adverse effects, mood, quality of sleep and any problems with daily activities.
When to refer
Consider referral to a pain clinic and/or condition-specific service at any stage (including initial presentation) if:
Pain is severe.
Pain significantly limits activity.
The underlying condition has deteriorated.
Management of autonomic neuropathy
See the separate Autonomic neuropathy article. In all patients, optimise control of diabetes.
Cardiovascular effects - various cardio-active drugs are being used to reverse the effects on the cardiovascular system, including angiotensin-converting enzyme (ACE) inhibitors, beta-blockers, diuretics and digoxin6.
Erectile dysfunction: see the separate Erectile dysfunction article.
Gastroparesis:7
Investigation using radiological or radioisotope methods may help in the diagnosis.
Investigation of cardiovascular autonomic neuropathy may help in the diagnosis.
Drugs which increase gastric emptying are worth trying. These include metoclopramide, domperidone and erythromycin.
Electrical stimulation has produced benefits in some patients.
Diabetic nocturnal diarrhoea:
Investigation must exclude other causes of intestinal upset.
May be helped by high doses of codeine, loperamide or diphenoxylate.8
Gustatory sweating:
Explanation and counselling are often required.
The anticholinergic agent glycopyrrolate is sometimes effective when applied topically.9
Postural hypotension:
Considering the possibility of contributory sympathetic nervous system damage for adults with diabetes who lose the warning signs of hypoglycaemia.
Considering the possibility of autonomic neuropathy affecting the gut in type 1 diabetes in adults who have unexplained diarrhoea, particularly at night.
Taking care when prescribing antihypertensive medicines or tricyclic antidepressants not to expose people to the risks of orthostatic hypotension as a result of the combined effects of sympathetic autonomic neuropathy and blood pressure-lowering medicines.
In adults with diabetes who have bladder emptying problems, investigating the possibility of autonomic neuropathy affecting the bladder, unless other explanations are adequate.
When managing the symptoms of autonomic neuropathy, including standard interventions for the manifestations encountered (eg, abnormal sweating and postural hypotension).
Acute painful neuropathy of rapid improvement of blood glucose control3
Acute painful neuropathy resulting from rapid improvement of blood glucose control is a self-limiting condition that improves symptomatically over time.
The specific treatments for acute painful neuropathy resulting from rapid improvement of blood glucose control aim to make the symptoms tolerable until the condition resolves; they may not relieve pain immediately and may need to be taken regularly for several weeks to be effective.
Use of simple analgesics (paracetamol, aspirin) and local measures (bed cradles) are recommended as a first step; however, if trials of these measures are ineffective, they should be stopped and other measures tried.
Diabetes control should not be relaxed to address acute painful neuropathy resulting from rapid improvement of blood glucose control in adults with type 1 diabetes.
If simple analgesia does not provide sufficient pain relief for adults with type 1 diabetes who have acute painful neuropathy resulting from rapid improvement
of blood glucose control, treatments for neuropathic pain should be offered (see above).
Prognosis13
Autonomic neuropathy is associated with a high mortality rate, mainly due to its association with chronic kidney disease, cardiopathy and hypotension. For most patients with peripheral neuropathy, the quality of life is poor.
Diabetic peripheral neuropathy is a major cause of morbidity and increased mortality and increases the risk of burns, injuries and foot ulceration.14
Less than a third of patients achieve reasonable pain control.
People with diabetes are more likely to undergo lower limb amputation.15
Prevention of diabetic neuropathy
Tight glycaemic control has been clearly shown to reduce the risk of neuropathy.
Smoking avoidance or cessation.
Further reading and references
- Diabetes UK
- Diabetes; NICE
- Yang H, Sloan G, Ye Y, et al; New Perspective in Diabetic Neuropathy: From the Periphery to the Brain, a Call for Early Detection, and Precision Medicine. Front Endocrinol (Lausanne). 2020 Jan 17;10:929. doi: 10.3389/fendo.2019.00929. eCollection 2019.
- Chang MC, Yang S; Diabetic peripheral neuropathy essentials: a narrative review. Ann Palliat Med. 2023 Mar;12(2):390-398. doi: 10.21037/apm-22-693. Epub 2023 Feb 8.
- Shakher J, Stevens MJ; Update on the management of diabetic polyneuropathies. Diabetes Metab Syndr Obes. 2011;4:289-305. doi: 10.2147/DMSO.S11324. Epub 2011 Jul 21.
- Type 1 diabetes in adults: diagnosis and management; NICE Guidelines (August 2015 - last updated August 2022)
- Vinik AI, Erbas T; Diabetic autonomic neuropathy. Handb Clin Neurol. 2013;117:279-94. doi: 10.1016/B978-0-444-53491-0.00022-5.
- Neuropathic pain – pharmacological management: The pharmacological management of neuropathic pain in adults in non-specialist settings; NICE Clinical Guideline (November 2013, latest update September 2020)
- Balcioglu AS, Muderrisoglu H; Diabetes and cardiac autonomic neuropathy: Clinical manifestations, cardiovascular consequences, diagnosis and treatment. World J Diabetes. 2015 Feb 15;6(1):80-91. doi: 10.4239/wjd.v6.i1.80.
- Krishnasamy S, Abell TL; Diabetic Gastroparesis: Principles and Current Trends in Management. Diabetes Ther. 2018 Jul;9(Suppl 1):1-42. doi: 10.1007/s13300-018-0454-9. Epub 2018 Jun 22.
- Nightingale JMD, Paine P, McLaughlin J, et al; The management of adult patients with severe chronic small intestinal dysmotility. Gut. 2020 Aug 21. pii: gutjnl-2020-321631. doi: 10.1136/gutjnl-2020-321631.
- Pop-Busui R, Boulton AJ, Feldman EL, et al; Diabetic Neuropathy: A Position Statement by the American Diabetes Association. Diabetes Care. 2017 Jan;40(1):136-154. doi: 10.2337/dc16-2042.
- Postural hypotension in adults: fludrocortisone; NICE Evidence summary, October 2013
- Veazie S, Peterson K, Ansari Y, et al; Fludrocortisone for orthostatic hypotension. Cochrane Database Syst Rev. 2021 May 17;5(5):CD012868. doi: 10.1002/14651858.CD012868.pub2.
- Type 2 diabetes in adults: management; NICE Guidance (December 2015 - last updated June 2022)
- Bodman MA, Dreyer MA, Varacallo M; Diabetic Peripheral Neuropathy.
- Tesfaye S, Selvarajah D; Advances in the epidemiology, pathogenesis and management of diabetic peripheral neuropathy. Diabetes Metab Res Rev. 2012 Feb;28 Suppl 1:8-14. doi: 10.1002/dmrr.2239.
- Adams CT, Lakra A; Below-Knee Amputation.
Article history
The information on this page is written and peer reviewed by qualified clinicians.
Next review due: 20 Oct 2027
21 Oct 2024 | Latest version
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