Severe Diabetic Ketoacidosis in Two Children with New Onset type 1 Diabetes after SARS-CoV-2 Infection
Caroline Ponmani1*, Tony Hulse2 and Sophia D Sakka Sophia2,3
1Department of Paediatric Emergency Medicine, Barking, Havering and Redbridge NHS Foundation Trust, UK
2Department of Endocrinology and Diabetes, Evelina London Children’s Hospital, UK
3GKT School of Medical Education, King’s College London Faculty of Life Sciences and Medicine, UK
Submission: March 27, 2021; Published: April 07, 2021
*Corresponding author: Caroline Ponmani, Consultant in Paediatric Emergency Medicine, Department of Paediatric Emergency Medicine, Barking Havering and Redbridge NHS Foundation Trust, Rom Valley Way RM7 0AG, London, UK
How to cite this article: Caroline P, Tony H, Sophia D Sakka S. Severe Diabetic Ketoacidosis in Two Children with New Onset type 1 Diabetes after SARS-CoV-2 Infection. Curre Res Diabetes & Obes J 2021; 14(3): 555887. DOI: 10.19080/CRDOJ.2021.14.555887
Abstract
Background: An increase in the incidence and the severity of diabetic ketoacidosis (DKA) in children with new onset type1 diabetes has been reported in the COVID-19 pandemic. Studies have linked this to SARS-CoV-2 although causality could not be established.
Methods: We report two children with new onset type 1 diabetes and serum autoantibodies against islet cells and glutamic acid decarboxylase who developed severe DKA following infection with SARS-CoV-2. Both tested positive for COVID -19 PCR from nasopharyngeal swabs and developed symptoms of severe DKA, shock and cerebral oedema. Both children deteriorated rapidly illustrating the combined synergistic effects of the inflammatory pathways of COVID -19 and DKA.
Results: Both children needed admission to intensive care. The first child had raised inflammatory and cardiac markers and was suspected to have Paediatric multisystem inflammatory syndrome temporarily associated with COVID-19 (PIMS-TS). The period of type 1 diabetes symptoms was short in the second child, she also presented with clinical and biochemical features of pancreatitis which improved with supportive management. She also presented with thyrotoxicosis at the time of diagnosis.
Conclusion: Our report shows the association between infection with SARS-CoV-2 and rapid decompensation to DKA possibly accelerating the development of new-onset type 1 diabetes in genetically predisposed children. Additionally, the second child had pancreatitis illustrating that SARS-CoV-2 can affect both the endocrine and the exocrine function of the pancreas. Enhanced vigilance and earlier intervention is needed to prevent decompensation to DKA.
Keywords: Diabetic ketoacidosis; Type 1 diabetes; SARS CoV-2; Acute hyperglycaemia; Glucose
Abbreviations: DKA: Diabetic Ketoacidosis; ED: Emergency Department; GP: General Practitioner; GCS: Glasgow Coma Scale; IV: Intravenous; PICU: Paediatric Intensive Care Unit
Introduction
Increase in the incidence and the severity of DKA in children with new onset type 1 diabetes during the COVID-19 pandemic has been reported from several published studies although causality could not be established [1,2]. Studies also indicate a link between COVID-19 and acute hyperglycaemia in adults infected with SARS-CoV-2 [3,4]. In vitro studies have shown that the virus itself may trigger the development of ketoacidosis via direct damage to pancreatic beta cells [5,6]. Our report shows the association between infection with SARS-CoV-2 and rapid decompensation to DKA in two children with new onset type 1 diabetes.
Case 1
A 10-year-old Caucasian girl presented to the Emergency Department (ED) in May 2020 with a two day history of difficulty in breathing and a one day history of lethargy. She presented to the general practitioner (GP) initially, a diagnosis of asthma was made and she was prescribed Salbutamol inhaler. The next day she developed slurred speech, was unable to walk and was brought to ED by parents. Parents reported that she had a four-month history of gradual weight loss and six weeks of polyuria and polydipsia (Figure 1). She presented with fluid refractory shock and a fluctuating Glasgow Coma Scale (GCS) of 11-13. Her initial blood gas showed a pH 6.91, base deficit of 27, HCO3 of 2.6 mEq/l and glucose of 37mmol/l.
She was diagnosed with new onset type 1 diabetes with severe
DKA and shock. She was suspected to have cerebral oedema.
Intravenous (IV) fluids followed by insulin infusion were started,
but went on to need inotropic support. She was also started on
IV Ceftriaxone. PIMS-TS was suspected due to her clinical picture
and raised inflammatory and cardiac markers [CRP: 215mg/L,
WBC: 11.3 x 109 L, Procalcitonin: 5.32 ug/L (0-0.05), Ferritin:
490ug/L (14-101), troponin: 35 (0-13ng/L), D-dimers: 4.66 mg/L
(0-0.55)] and she was transferred to the Paediatric intensive
care unit (PICU). She needed treatment in PICU for 4 days, her
neurology improved with DKA management and she did not need
hyperosmolar treatment. She did not receive treatment for PIMS
–TS as she did not fulfil all the criteria.
CT head and echocardiography were normal. Her blood
cultures were negative. Her nasopharyngeal swab was positive
for COVID -19. On day 5, she was transferred to the paediatric
ward, and subcutaneous insulin therapy was initiated. Over the
course of the next few days her blood glucose levels stabilized.
She received an educational programme on diabetes mellitus
management and was discharged home on subcutaneous insulin
injections. Her weight was 46 kg, height was 153cm and BMI was
19.52 kg/m2. She had raised serum autoantibodies against islet
cells and glutamic acid decarboxylase, confirming the diagnosis of
type 1 diabetes. There is a strong family history of diabetes. Her
father, paternal grandfather and both maternal grandparents have
type 2 diabetes. Mother’s first cousin has type 1 diabetes.
Case 2
A second child, a 13 year old Afro Caribbean girl presented to ED in January 2021 with a one day history of difficulty in breathing. She also went on to develop abdominal pain and vomiting and became increasingly lethargic over the day. She became unresponsive and was brought to ED. Parents reported that she had polyuria and polydipsia for 2 weeks (Figure 1). She was in shock and had a fluctuating GCS of 9-12. Her initial blood gas showed a pH 6.86, base deficit of 28.5, HCO3 of 6.4 mEq/l and glucose of 45 mmol/l. Her WBC count was raised 37.6 x 109 L with raised neutrophils of 31.1x 109 L, urea of 17.8 mmol/L, Creatinine of 218 umol/l , HbA1c of 105mmol/ mol ,CRP of 7, amylase of 1200(30-100U/L), lipase of 314 IU/L(10-180 IU/L), C peptide of 435pmpl/L and insulin of 14.6 miu/L. She was diagnosed with new onset type 1 diabetes with severe DKA, shock and pancreatitis. IV fluids followed by insulin infusion were started. She was transferred to PICU. She improved with management of DKA, did not need hyperosmolar therapy and was transferred to the paediatric ward after 48 hours. Pancreatitis improved with supportive management, her repeat amylase was and 392 IU/L and lipase was 328IU/L. Ultrasound abdomen was normal. Over the course of the next few days her blood glucose levels stabilized. She received education on diabetes mellitus management and was discharged home on subcutaneous insulin injections. Her blood culture did not show growth of any organisms. COVID -19 PCR was positive from nasopharyngeal swab. She had serum autoantibodies against islet cells and glutamic acid decarboxylase confirming the diagnosis of type 1 diabetes. At diagnosis she was also found to have raised fT4 25.3pmol/L (12.6-21pmol/L) with suppressed TSH of 0.01mU/L (0.5-4.3 mU/L), but with no symptoms of hyperthyroidism. They were repeated after DKA was treated and remained abnormal, along with positive TSH Receptor antibodies of 1.79u/ml (normal range <0.04 IU/ml), confirming the diagnosis of Graves disease. Her weight was 44 kg, height was 166 cm and BMI of 15.97 kg/ m2. There is a strong family history of diabetes, both maternal grandparents and paternal grandfather have type 2 diabetes.
Discussion
Analysis of the timeline of both cases raised the question - Is
SARS-Co-2 accountable for the incidence and the severity of DKA
in the children?
Historically, viruses have been suspected to be the triggers
in the onset and progress of type 1 diabetes in a genetically
predisposed individual. However, it has been difficult to implicate
them as critical infectious event that initiates autoimmunity
predate clinical onset of type 1 diabetes by months to years [7].
Recent in vitro studies have shown that SARS-Co-2 itself may
trigger the development of ketoacidosis via direct damage to
pancreatic β-cell cells [1].
Investigation of the timeline of the onset and progress of
symptoms in the first child showed that she had symptoms of
type 1 diabetes (polyuria polydipsia and weight loss) preceding
the onset of infection with SARS-CoV- 2. Infection with the
virus appears to have precipitated DKA. In the second child the
period of type 1 diabetes symptoms were of very short duration,
she developed symptoms of difficulty in breathing, she also
had severe epigastric pain and vomiting with a raised amylase
and lipase and was diagnosed with pancreatitis illustrating
the exocrine component of infection with SARS-CoV- 2. Both
children had type 1 diabetes antibodies and patient 2 has thyroid
receptor antibodies, indicating the presence of an underlying
autoimmunity making it less likely that the virus was causal for
type 1 diabetes. However, the severity of DKA in both and the
short duration of type 1 diabetes symptoms in the second child
illustrates that infection with SARS–CoV–2 resulted in rapid loss
of β-cells resulting in severe DKA. The inflammatory cascades of
the COVID -19 infection and DKA may have acted synergistically
contributing to the severity of the clinical manifestations in both
children.
Delay in presentation to ED due to parental fears of COVID -19
resulting in DKA in children with new onset type 1 diabetes has
been reported in some [8,9] but not all studies [3]. There is an
intrinsic delay in the recognition of paediatric diabetes due to the
low volume presentation in children and nonspecific symptoms.
Children have the ability to compensate making recognition
difficult until they deteriorate rapidly. In the first patient, parents
noticed polydipsia and increased sleeping but attributed these
symptoms to boredom due to lockdown. Parents sought help
appropriately when she developed symptoms of difficulty in
breathing, initially from primary care where she was given
salbutamol inhalers. She became increasingly lethargic over the
next 24 hours and again parents correctly sought help bringing
her to ED. The second child had a short period of symptoms of 2
weeks duration. She self-diagnosed herself with type 1 diabetes
after reading up her symptoms on the internet but parents
were not convinced. Parents sought help from 111 when she
developed difficulty in breathing then brought her to ED when
she became unresponsive. We did not find delayed presentation
due to parental fears of COVID -19 to be a significant factor in the
decompensation to DKA in both children.
Diabetic patients have increased chances of developing
autoimmune thyroid disease [10]. Thyrotoxicosis also occurs
with increased frequency in diabetic children than in the general
population, but it usually present after the diagnosis of diabetes.
Autoimmune thyrotoxicosis at the time of type 1 diabetes
presentation, like in case 2, is quite rare [11] and raised the
question whether COVID-19 infection triggered an exacerbated
autoimmune response.
Conclusion
We present for the first time a descriptive study of two children who presented with new onset diabetes, developed severe DKA after infection with SARS- CoV- 2 and tested positive for COVID-19 PCR on nasopharyngeal swabs. The observations from our study have important implications in emphasizing the need to raise public and clinician awareness for early recognition and prevention of DKA especially in informing clinicians who may see children in the early phase of new onset diabetes. Additionally the period of type 1 diabetes symptoms was very short in the second child, a variation which has been reported in one other study.5 Further investigation is needed on whether children are presenting with a shorter duration of symptoms of type 1 diabetes in the pandemic. Whilst we illustrate that infection with SARSCoV- 2 contributed to DKA and accelerated the onset of diabetes, we acknowledge that more clinical research and additional qualitative and quantitative studies are needed. While we have progressed rapidly in advances in the treatment of paediatric type 1 diabetes the epidemiology is still shrouded in mystery, perhaps now is the time to learn from SARS – CoV -2 and its proposed affinity for pancreatic β-cells. In the meantime public and clinician awareness campaigns emphasizing recognition of diabetic ketoacidosis remains key.
Learning Points
Severe DKA in children with new onset type 1 diabetes is reported for the first time with proven SARS-CoV-2 infection. Viral triggers in the onset and progress of new onset type 1 diabetes have always been suspected, now may be the time to learn from SARS -CoV-2 and its proposed affinity for pancreatic β-cells.
Consent
Both families have consented to the publication of the cases.
Acknowledgement
With grateful thanks to Yvette Redpath, Paediatric Emergency
Department Clinical Fellow, Barking Havering and Redbridge NHS
Trust, Romford, UK.
Saima Khan, Paediatric Senior House Officer, Barking Havering
and Redbridge NHS Trust, Romford, UK.
Emma Jobson, Abby Billinghurst, Nicola Hammond, Staff
Nurses Paediatric Emergency Department, Barking Havering and
Redbridge NHS Trust, Romford, UK.
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