Background
Since the 1950s, metformin has been successfully used as a first-line pharmacotherapy for treating individuals with type II diabetes [
1]. Although it is considered as a drug with a broad safety profile, metformin-associated lactic acidosis (MALA) is a widely documented adverse event [
2,
3]. MALA is a rare condition associated with poor prognoses and has an estimated mortality of between 25 and 50% [
4]. It develops more frequently in elderly patients with impaired kidney function and liver failure [
5]
It has been established that a pH bellow 7.35, a high lactate level, and compatible symptomatology are key elements in detecting the presence of MALA [
5]. The anion gap, which measure the difference between cations and anions in serum, is an useful tool when attempting to identify the cause of metabolic acidosis. Despite a high anion gap being considered one of the main causes of metabolic acidosis, it is still uncertain whether there is an association between an anion gap and MALA diagnosis. In this report, we present a case series of suspected MALA patients with the aim of highlighting the importance of the anion gap value in MALA diagnoses.
Case presentation
Cases involving six Caucasian patients with suspected MALA who visited the emergency department between September 2019 and December 2019 were analysed. The main characteristics of these patients are presented in Table
1. The mean age was 75.5 (standard deviation = 6.3) years. All the patients exhibited respiratory symptoms at admission; further, based on a blood gas analysis performed at emergency department admission, almost all of them presented with a pH value < 7.35 and lactate level > 2 mmol/L while only one patient had a lactate level of > 5 mmol/L, which is one of the established criteria for an MALA diagnosis [
7]. Lactate level was analysed by the “GEM premier 3500 in Instrumentation Laboratory” automated blood gas analysis system blood gas analyser (ABL90, Radiometer, Bronshoj, Denmark). Alternative causes of metabolic acidosis such concomitant drugs or toxics substances were excluded, based on medical history review and patients or relatives interview. Four patients presented with chronic kidney disease as a comorbidity. However, the estimated glomerular filtration rate (calculated by the modification of diet in renal disease (MDRD) formula [
6]) was less than 30 mL/min at admission in all cases. All the patients had metformin plasma concentrations above the upper limit of the therapeutic range (> 2.5 mg/L) [
7]. The highest metformin concentrations were not found in patients with the highest lactate values.
Table 1
Characteristics of patients included
1 | 73 | No | 7.87 | 34.7 | 7.07 | 12.5 | 37.7 | 36.6 | Si |
2 | 77 | Yes | 2.02 | 10.32 | 7.03 | 2.7 | 16.7 | 17.1 | No |
3 | 82 | Yes | 4.14 | 44.66 | 7.13 | 2.8 | 12.3 | 14.2 | Si |
4 | 64 | No | 7.85 | 15.8 | 6.74 | 7.9 | 39.3 | 44.8 | No |
5 | 78 | No | 1.86 | 18.1 | 7.30 | 2 | 14.2 | 12.2 | No |
6 | 79 | Yes | 4.68 | 8.27 | 7.21 | 5.7 | 16.3 | 24.9 | No |
Only two of the included patients met the haemodialysis criteria established by the extracorporeal treatments in poisoning (EXTRIP) recommendations [
8] (lactate > 20 mmol/L, pH ≤ 7.0, or failure of standard treatment, including bicarbonate); further, only one of them received haemodialysis, and therefore, the therapeutic effort upon admission was limited to the other patient. Two patients died during hospitalisation, and these patients had the highest metformin plasma concentrations (> 30 mg/L). The anion gap values (calculated as [Na
+] + [K
+] − [Cl
−] − [HCO
3−]) ranged from 12.3 to 39.3, with only two patients exhibiting values greater than 14.
Discussion and conclusions
The results of our series demonstrate that in the case of severe metformin intoxication, the anion gap value may be normal or slightly elevated, with no relation to the metformin plasma concentrations. Anion gap alterations can occur in different situations involving acid-base imbalance, and monitoring these alterations is a useful approach in determining the aetiology of metabolic acidosis. One of the most common causes is lactic acidosis. Metformin inhibits cellular mitochondrial respiration, causing an increase in anaerobic metabolism and lactate production [
9]. This situation leads to type B lactic acidosis [
10] that overlaps with type A lactic acidosis due to hypoperfusion in patients with haemodynamic failure in case of systemic collapse.
The association between severity and mortality on admission and the lactate value is well known. However, the association between the anion gap value and mortality remains unclear. The sensitivity of using the anion gap has been reported to be poor in detecting the levels of acidosis when it is mediated by lactate [
11]. In our patients, we observed that very high concentrations of metformin with an increase in lactate levels did not lead to a relevant increase in the anion gap. Therefore, this series reinforces the view that measuring the anion gap has limited utility in predicting the accumulation of this drug because of the different factors that can coexist in these patients. The toxicity found in our patients was possibly due to mixed acidosis caused by a combination of accumulated metformin, diabetic ketoacidosis, tissue hypoxia, and kidney failure, which resulted in a wide range of anion gap values. The absence of plasma albumin levels has prevented from obtaining corrected anion gap values, which is a limitation of our study since it could partly affect the results obtained. Among the limitations associated with our series, the one worth noting is that at admission, there was a lack of data on albumin levels that can significantly modify the value of the anion gap.
On the other hand, it is known that the severity of lactic acidosis is not proportional to metformin plasma concentrations, as patients described as having severe clinical symptoms exhibited slightly elevated concentrations, and those without MALA had high concentrations of metformin; despite these findings, high concentrations have been associated with higher mortality rates in patients with MALA [
12]. The small sample size in our series prevented us from drawing conclusions regarding the association between metformin concentrations and mortality. Despite this, we observed that the patients with the highest metformin concentrations were those who died, which contributes to fuelling this debate.
Likewise, changes in pH, lactate levels, and bicarbonate values are critical for making a selection among therapeutic options. It should be noted that only one of the six patients had a lactate value of > 5 mmol/L, an established criterion for the diagnosis of MALA [
5]. However, all the patients in our series had serious clinical conditions. For this reason, it must be considered that lower levels of lactate may indicate significant accumulations of metformin and severe clinical presentations, given that the anion gap value could not aid in diagnosing these cases.
Two of the six patients (33.3%) died during hospitalisation. Previous studies have reported mortality rates between 25 and 50% [
4], highlighting the severity of this complication. Despite the fact that owing to its benefits in terms of the incidence of cardiovascular events and mortality, metformin is recommended by different guidelines for patients with mild or moderate impairment of renal function with an adequate dose adjustment [
1], elderly patients often exhibit a sudden deterioration of renal function secondary to different circumstances. Our patients presented with very high metformin concentrations, which probably indicate renal function deterioration that evolved for several days before hospitalisation. The high distribution volume of metformin facilitates its extensive accumulation, which makes it difficult to establish a relationship between plasma levels and severe lactic acidosis [
9]. For this reason, this drug should be suspected as a possible causative agent of acidosis in patients with relevant deterioration of renal function.
This case series shows that in patients with MALA, there are significant variations in the anion gap value, which is not related to the level of accumulated metformin, and therefore, it is doubtful whether calculating the anion gap could be used an approach for MALA diagnosis.
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