Euglycemic diabetic ketoacidosis:A missed diagnosis

Prashant Nasa,Sandeep Chaudhary,Pavan Kumar Shrivastava,Aanchal Singh

Prashant Nasa,Aanchal Singh,Department of Critical Care Medicine,NMC Specialty Hospital,Dubai 7832,United Arab Emirates

Sandeep Chaudhary,Department of Endocrinology,NMC Specialty Hospital,Dubai 7832,United Arab Emirates

Pavan Kumar Shrivastava,Department of Internal Medicine,NMC Specialty Hospital,Dubai 7832,United Arab Emirates

Abstract Euglycemic diabetic ketoacidosis(DKA)is an acute life-threatening metabolic emergency characterized by ketoacidosis and relatively lower blood glucose(less than 11 mmol/L).The absence of hyperglycemia is a conundrum for physicians in the emergency department and intensive care units;it may delay diagnosis and treatment causing worse outcomes.Euglycemic DKA is an uncommon diagnosis but can occur in patients with type 1 or type 2 diabetes mellitus.With the addition of sodium/ glucose cotransporter-2 inhibitors in diabetes mellitus management,euglycemic DKA incidence has increased.The other causes of euglycemic DKA include pregnancy,fasting,bariatric surgery,gastroparesis,insulin pump failure,cocaine intoxication,chronic liver disease and glycogen storage disease.The pathophysiology of euglycemic DKA involves a relative or absolute carbohydrate deficit,milder degree of insulin deficiency or resistance and increased glucagon/insulin ratio.Euglycemic DKA is a diagnosis of exclusion and should be considered in the differential diagnosis of a sick patient with a history of diabetes mellitus despite lower blood glucose or absent urine ketones.The diagnostic workup includes arterial blood gas for metabolic acidosis,serum ketones and exclusion of other causes of high anion gap metabolic acidosis.Euglycemic DKA treatment is on the same principles as for DKA with correction of dehydration,electrolytes deficit and insulin replacement.The dextrosecontaining fluids should accompany intravenous insulin to correct metabolic acidosis,ketonemia and to avoid hypoglycemia.

Key Words:Diabetic Ketoacidosis;Sodium/glucose co-transporter-2 inhibitors;Pregnancy with diabetic ketoacidosis;Diabetes complications;Pregnancy in diabetes;Ketosis;Metabolic acidosis

INTRODUCTION

Diabetic ketoacidosis(DKA)is widely known as a life-threatening acute complication of diabetes mellitus(DM).It mainly occurs in patients with type 1 DM;however,any acute illness like infection,trauma or acute coronary syndrome may also trigger DKA in type 2 DM.Hyperglycemia(plasma glucose >14 mmol/L)is a hallmark in the diagnosis of DKA completing the triad with metabolic acidosis and ketonemia[1,2].

Euglycemic DKA is defined as ketoacidosis(pH <7.3 or serum bicarbonate <18 mmol/L)with either near-normal plasma glucose or a milder degree of hyperglycemia(11-14 mmol/L)[3,4].The absence of hyperglycemia can conceal the underlying DKA creating a diagnostic dilemma especially in the emergency department,which is associated with worse outcomes[3-5].Dehydration in euglycemic DKA is also minor in the absence of polyuria and polydipsia.Patients may present instead with malaise,anorexia and tachypnoea because of ketonemia and accompanying ketoacidosis.The high index of suspicion with early testing for metabolic acidosis and blood ketones can identify these patients[4].

Euglycemic DKA was first described in 1973 by Munroet al[6]among type 1 DM.Euglycemic DKA is an uncommon diagnosis with an incidence ranging between 2.6%to 3.2% of admissions with DKA[7,8].In a study by Munroet al[6],the incidence of euglycemic DKA had an incidence of 3.2%,using a plasma glucose cut-off of less than 16.7 mmol/L[8].However,the cut-off of plasma glucose used for euglycemic DKA in recent reviews is lower(either 14 mmol/L[3]or 11 mmol/L[4]).Authors have also used other terminology for euglycemia,like near-normal or lower than anticipated plasma glucose[9,10].The true incidence of euglycemic DKA is therefore unknown.With the introduction of sodium/glucose cotransporter-2(SGLT-2)inhibitors in DM management,there is a definitive increase in the published case reports or series on euglycemic DKA[9,11].The other common causes of euglycemic DKA are pregnancy and prolonged fasting.In this review,we will discuss the pathophysiology,diagnostic considerations and management of euglycemic DKA.

PATHOPHYSIOLOGY OF EUGLYCEMIC DKA

The pathophysiology of DKA is already very well-known,characterized by a relative or absolute deficiency of insulin and excess of counterregulatory(or counter responsive)hormones like glucagon,corticosteroids,catecholamines or growth hormones[1].The hormonal imbalance causes hyperglycemia by increasing glycogenolysis,hepatic gluconeogenesis and decreased peripheral utilization of glucose.It also promotes gluconeogenesis and ketogenesis from free fatty acid mobilization by lipolysis in adipose tissue and proteolysis of amino acids[1].Ketone bodies(betahydroxybutyrate,acetoacetate and acetone)are responsible for metabolic acidosis,while hyperglycemia through glycosuria and osmotic diuresis causes dehydration and hypovolemia(Figure 1).

Carbohydrate deficit has a pivotal role in the pathophysiology of euglycemic DKA,while insulin deficit or insulin resistance is relatively minor and secondary(Figure 1B).However,the counterregulatory hormone production is unabated,causing an increased glucagon/insulin ratio and triggering ketogenesis with no significant change in hepatic gluconeogenesis and peripheral glucose utilization[3,4,12].The precipitating causes for euglycemic DKA include fasting or prolonged physical activity with depleted hepatic glycogen stores and hence impaired glycogenolysis[3,12].Increased glucagon also promotes lipid oxidation,generating acetyl-CoA and ketone bodies when glycolysis intermediates are unavailable due to reduced intracellular glucose oxidation.The unabated ketonemia and glycosuria(seen usually with SGLT-2 inhibitors)contribute to euglycemic(or hypoglycemic)DKA[4,9].

The three common causes of euglycemic DKA are SGLT-2 inhibitors,pregnancy and prolonged fasting.

SGLT-2 inhibitors

SGLT-2 inhibitors are the latest group of medications added to the arsenal to treat patients with DM.Their promotion in type 2 DM is due to clinical trials suggesting protection against major adverse cardiovascular events and reduced hospitalization for heart failure and deaths[13].SGLT-2 inhibitors have also been shown to slow chronic kidney disease progression in type 2 DM[14,15].The added advantages appeared to be modest weight reduction and lower systolic blood pressure aside from its effect on hyperglycemia[13,15].SGLT-2 inhibitors act by blocking the SGLT-2 cotransporter located in the early proximal renal tubule,which is responsible for the reabsorption of most(80%-90%)of the glucose filtered by the glomerulus.It leads to glucosuria and resultant lowering of blood plasma glucose concentration[16,17].The exact mechanism that can precipitate DKA in susceptible individuals includes,osmotic diuresis along with glucosuria(causing a state of carbohydrate deficit),volume depletion and dehydration[9,16].Carbohydrate deficit and hypovolemia promote glucagon release,increase glucagon/insulin ratio and trigger ketogenesis with euglycemia.The other factors include the direct effect of SGLT-2 inhibitors on pancreatic alpha cells,causing glucagon release and inhibiting ketone bodies excretion by the kidneys[18,19].

There has been a steady increase in the published reports on DKA with the growing use of SGLT-2 inhibitors[9].The exact incidence rate of SGLT-2 inhibitors associated with DKA is unknown.The clinical trials of SGLT-2 inhibitors with type 2 DM have reported an incidence of 0.16 to 0.76 events per 1000 patient-years[9,20].In a sizeable multicentric cohort study by the Canadian Network for Observational Drug Effect Studies,the incidence of DKA with SGLT-2 inhibitors in type 2 DM was 1.40(1.29-1.53)per 1000 patient-years.The risk of DKA was nearly three-fold higher with SGLT-2 inhibitors than dipeptidyl peptidase-4 inhibitors.The increased risk of DKA was observed with all three SGLT-2 inhibitors suggesting a class effect,with canagliflozin(hazard ratio 3.58)having the highest risk[21].In an analysis of the Food and Drug Administration’s adverse event reporting system on DKA incidence with SGLT-2 inhibitors,there was a seven-fold increased risk,and around two-thirds of the reported DKA cases were euglycemic[22].The risk is higher in patients with significant insulin insufficiency or type 1 DM(up to 9%)[9,16].

The United States Food and Drug Administration has warned against the risk of DKA with SGLT-2 inhibitors and so far has not approved its use for type 1 DM[23].The risk of DKA with SGLT-2 inhibitors in type 1 DM varies widely across the published data of different randomized controlled trials,and factors responsible for such variation are not well understood.In a trial of dapagliflozin evaluation in patients with inadequately controlled type 1 diabetes[24],a significant number of patients in the dapagliflozin groups had DKA as compared to placebo at 52 weeks of follow-up.The risk of DKA was 4.0%,3.4% and 1.9% in the dapagliflozin 5 mg,10 mg and placebo groups,respectively.The DKA rate was also higher in the empagliflozin 10 mg and 25 mg groups compared with placebo in the empagliflozin as adjunctive to insulin therapy program[24].The DKA rate was 4.3% and 3.3% with empagliflozin 25 mg and 10 mg groups,respectively,compared to 1.2% in the placebo group.It corresponds to an incidence of 5.9,5.1 and 1.8 per 1000 patient-years[25],respectively.A similar rate of DKA has been observed in clinical trials of sotagliflozin and canagliflozin[26,27].

Figure 1 Ketone bodies(beta-hydroxybutyrate,acetoacetate and acetone)are responsible for metabolic acidosis,while hyperglycemia through glycosuria and osmotic diuresis causes dehydration and hypovolemia.A:Pathophysiology of diabetic ketoacidosis;B:Pathophysiology of euglycemic diabetic ketoacidosis.FFA:Free fatty acids;↑:Increase;↓:Decrease;~:No change.

The duration of SGLT-2 inhibitor treatment before a diagnosis of DKA onset is hugely variable in the literature(0.3-420 days)[28].In a recent meta-analysis by Mussoet al[29],the risk factors of DKA with SGLT-2 inhibitors in type 1 DM included(1)baseline body mass index >27 kg/m2;(2)insulin resistance calculated by estimated glucose disposal rate <8.3 mg/kg/min;(3)the ratio of total insulin dose reduction-tobaseline insulin sensitivity;and(4)degree of volume depletion.These risk factors should be considered by clinicians while using SGLT-2 inhibitors in type 1 DM to reduce the risk of DKA.Recently,the National Institute for Health and Care Excellence revised its guidance and recommended SGLT-2 inhibitors for the treatment of type 1 DM[30].The patients with a body mass index of 27 kg/m2or more,insulin requirement of 0.5 units/kg of body weight/day or more and inadequate glycemic control despite optimal insulin therapy can be considered for the addition of dapagliflozin with insulin under supervision of a physician.However,the patient should receive education on the risk,signs and symptoms of DKA.They should also be trained on home monitoring of blood ketones and on appropriate action-plan in case of elevated blood ketones[30].

DKA in patients on SGLT-2 inhibitors can be precipitated by one of these causes(Table 1).The excessive reduction(>50%)or omission of insulin doses,insulin pump failure or malfunction,a low carbohydrate diet,nausea and vomiting induced by other drug combination like glucagon-like peptide 1 agonists,excessive alcohol intake,acute stressful conditions like myocardial infarction,heart failure,infections or fever,trauma and surgery[9,10].The SGLT-2 inhibitor prescription in a new-onset DM without establishing the mechanism of hyperglycemia can also precipitate DKA in undiagnosed type 1 DM[28].

Pregnancy

DKA incidence in pregnancy is significantly higher than in nonpregnant females(8.9%vs3.1%)and associated with lower blood glucose levels and increased perinatal morbidity and mortality[31,32].There are various case reports of euglycemic DKA in pregnancy with type 1 DM,type 2 DM and gestational DM[32-36].The physiological changes of pregnancy include hypoinsulinemia and carbohydrate deficit to match the glucose requirement of the fetus and placenta[31,35,36].The respiratory alkalosis seen with pregnancy and compensatory urinary loss of bicarbonate reduces the body reserves to buffer metabolic acidosis.There is also an insulin resistance caused by counterre-gulatory pregnancy hormones(progesterone,estrogen,human placental lactogen and tumor necrosis factor-α)seen during the second and third trimester of pregnancy.Euglycemia DKA is also common during pregnancy due to physiological hemodilution of blood glucose and increased glomerular filtration rate withglucosuria[31,35,36].Any acute illness like infection,vomiting,fasting or short starvation can trigger ketogenesis in pregnancy.Ketogenesis and metabolic acidosis during pregnancy occur faster than when not pregnant and at lower blood sugar levels[31,35,36].Any unexplained acidosis with a history of nausea,vomiting and decreased intake in a pregnant should raise a suspicion of euglycemic DKA[4].

Table 1 Precipitating causes for euglycemic diabetic ketoacidosis and their mechanisms

Fasting

Low-calorie intake,especially with intercurrent illness in patients with type 2 DM,can precipitate DKA with euglycemia[37,38].Patients with type 1 DM who do not adjust their insulin to low carbohydrate intake while fasting or ill can also develop euglycemic DKA[38,39].Fasting produces a carbohydrate deficit and depletion of glycogen stores leading to alternative energy sources like free fatty acids and lipolysis[39].Continued intake of insulin and depleted glycogen stores maintain a euglycemic state while lipolysis and ketogenesis remain unabated,triggering euglycemic DKA.A very restricted carbohydrate diet or starvation can also cause euglycemic DKA in patients without DM[4].The fasting-induced euglycemic DKA must be differentiated from starvation ketosis in which metabolic acidosis is not present(serum bicarbonate >18 mmol/L)[4,40].However,euglycemic DKA during fasting or starvation is familiar with type 1 DMvsnondiabetic patients.

The keto diet,characterized by a low carbohydrate and high fat diet,is promoted as a popular weight-loss method and other physical or metabolic benefits[41,42].The carbohydrate deficit and excess of fatty acids promote ketogenesis and divert ketones bodies as a source of nutrition.The weight loss is caused by reduced insulin requirement,ketone-induced osmotic diuresis and decreased oral intake because of ketonemia.The keto diet has been tried effectively in type 2 DM with weight loss benefits,better glycemic control and medication reduction for a short duration[42-45].The benefit is found more in patients with obesity and rigorous compliance with the diet.However,the long-term effects on glycemic control,adherence and safety in patients with DM are unproven[45].The keto diet can precipitate DKA in type 2 DM,especially during pregnancy or SGLT-2 inhibitors with a higher incidence of euglycemic DKA[44-49].The safety of the keto diet has not been demonstrated in type 1 DM due to the risk of ketonemia and hypoglycemia[42,50].

Other causes

Euglycemic DKA has been rarely reported with other conditions like bariatric surgery[51-53],acute pancreatitis[54],sepsis[36,55],cocaine intoxication[56],insulin pump failure[56]and gastroparesis[57].The patients undergoing bariatric surgery are prone to DKA because of perioperative deficient carbohydrate diet and prolonged fasting[4,53].Euglycemic DKA risk is higher in type 1 DM,patients on SGLT-2 inhibitors and prolonged perioperative fasting during bariatric surgery[51,52].Exogenous insulin administration in patients with DKA while en route to the hospital can also present lower blood glucose on admission[1].

DIAGNOSIS

Euglycemic DKA is an acute life-threatening medical emergency.The absence of hyperglycemia delays euglycemic DKA diagnosis in the emergency department or intensive care unit[3,4].However,euglycemic DKA is a diagnosis of exclusion,and other causes of high anion gap metabolic acidosis must be excluded[3].The common causes of high anion gap metabolic acidosis are alcoholic intoxication(excessive ethanol or toxic alcohols like methanol or polyethylene glycol),sepsis,lactic acidosis,drug overdoses(salicylate and tricyclic antidepressants)and renal failure.Other differential diagnoses include alcoholic ketoacidosis,chronic liver disease,starvation ketosis and glycogen storage disease.

Alcoholic ketoacidosis is seen in patients with chronic alcoholism[3,7].The patient is in a state of chronic carbohydrate deficit and is dependent on alcohol for calories.Any acute illness that can cause an inability to consume alcohol triggers ketonemia and ketoacidosis.The presentation is similar to euglycemic DKA with gastrointestinal symptoms(nausea,vomiting or abdominal pain),metabolic acidosis and ketonemia.Some authors consider alcoholic ketoacidosis as a subtype of euglycemic DKA[3,7].The pathophysiology is also similar with an increased glucagon/insulin ratio.However,a history of binge alcohol consumption,nondiabetic and hypoglycemia instead of euglycemia helps diagnose alcoholic ketoacidosis[58].The ketone bodies in alcoholic ketoacidosis are predominantly β-hydroxybutyrate(instead of acetoacetate),which could not be detected on routine urine strip testing[59].Serum ketones must be used for detection of ketonemia in the cases of suspicion of alcoholic ketoacidosis.

Euglycemic ketoacidosis because of either fasting or any intercurrent illness with reduced calorie intake needs to be differentiated from starvation ketosis[4,40].No previous history of DM,no intercurrent illness and hypoglycemia differentiate starvation ketosis.The metabolic acidosis is also not profound,with bicarbonate levels usually more than 18 mmol/L.

Sepsis[36,55]with or without associated lactic acidosis is a common presentation in an emergency that can conceal euglycemic DKA.High lactate levels with the absence of serum ketones help in the diagnosis of sepsis.

Unexplained high anion gap metabolic acidosis in a patient with DM and associated risk factors should raise suspicion of euglycemic DKA.A detailed history of risk factors like pregnancy,surgery,fasting,infections and SGLT-2 inhibitors should be evaluated(Table 1).The laboratory tests include serum and urine ketones,electrolytes(including calcium and magnesium),glucose,renal function(creatinine,blood urea nitrogen),blood gas analysis(venous or arterial),lactic acid,chest radiograph and electrocardiogram.Wide osmolar gap(the difference between measured and calculated serum osmolarity),inebriate state and multiorgan involvement help to diagnose toxic alcohol ingestion.History and symptoms of infection with laboratory tests showing leukocytosis,procalcitonin,organ dysfunction and lactate help diagnose sepsis and septic shock.

TREATMENT

The treatment is straightforward once the diagnosis is made.The treatment is based on the same principles as in DKA[1]:Insulin to correct metabolic acidosis and anion gap and correction of electrolytes and dehydration.The fluid resuscitation is similar to DKA with correction of dehydration and starts with balanced crystalloids.Insulin replacement using a fixed rate intravenous insulin infusion calculated on 0.1 units/per kilogram body weight should be continued until anion gap(metabolic acidosis)correction,and the patient can accept orally.However,an early glucose requirement(for prevention of hypoglycemia)allows concomitant insulin infusion to suppress ketogenesis[3].Dextrose(10% or 5%)and intravenous infusion of insulin must be used until the anion gap and metabolic acidosis is corrected.The resolution of DKA is defined as pH >7.3 units,bicarbonate >15.0 mmol/L and blood ketone level <0.6 mmol/L[1].Patients may require intensive care unit admission and monitoring for hemodynamic and electrolyte disturbances.The laboratory monitoring for acidosis,glucose and electrolytes must be similar to DKA management.

PREVENTION OF EUGLYCEMIC DKA

The patients who are prescribed SGLT-2 inhibitors should be explained the risk factors of DKA(Table 1).The off-label use of SGLT-2 inhibitors in type 1 DM should be done with close monitoring,starting with a lower dose,personalized insulin reduction regimen and patient education on carbohydrate intake[9,10].Patient education on“sick days” and other lifestyle modifications are essential and should be done in patients with type 1 and type 2 DM[9].Education about stopping SGLT-2 inhibitors when feeling ill or feverish,prolonged exercise,fasting or excessive alcohol intake must be done.The drug should also be stopped 3-4 days before planned surgery and adjust the insulin regimen accordingly[9,10].

CONCLUSION

Euglycemic DKA can be a missed diagnosis in the emergency department with worse outcomes.The presence of metabolic acidosis in a patient with DM and risk factors should be assessed for ketonemia,even in the absence of hyperglycemia.Patients on SGLT-2 inhibitors must be educated about risk factors and dose adjustment for sick days.