Fulminant type 1 diabetes mellitus associated with Coxsackievirus type B1 infection during pregnancy: a case report

Abstract

Background

Fulminant type 1 diabetes is characterized by an intrinsic insulin deficiency resulting from the severe destruction of pancreatic β cells and it rapidly leads to ketoacidosis. However, the association between fulminant type 1 diabetes in pregnancy and specific viral infections has not been reported.

Case presentation

The patient in this study was a 31-year-old Japanese woman, and at 30 weeks of pregnancy she was admitted with marked fatigue. Fetal bradycardia was noted, and the child was delivered by emergency cesarean section but was stillborn. The maternal blood sugar level was high (427 mg/dL), but the glycated hemoglobin value was 6.2%; therefore, fulminant type 1 diabetes was suspected. Serum antibody testing confirmed a Coxsackievirus B1 infection. The patient in this case had fulminant type 1 diabetes in pregnancy associated with Coxsackievirus B1.

Conclusion

This case highlights that fulminant type 1 diabetes in pregnancy may be associated with Coxsackievirus B1 infection.

Introduction

Fulminant type 1 diabetes (FT1D) is a subtype of type 1 diabetes (T1D); it is characterized by the abrupt onset of insulin-deficient hyperglycemia and ketoacidosis within a few days [1].

The specific etiology and pathogenesis of FT1D are unclear and may be related to genetic predisposition, autoimmunity, viral infection, and pregnancy.

Viral infection is strongly associated with fulminant diabetes, as reported previously, and can be associated with frequent flu-like symptoms along with a seasonal variation in time of onset. A viral infection is suggested to play a role in rapid β cell destruction.

Epidemiological studies have indicated an association between enteroviruses (EVs) and T1D [2]. Certain class II human leukocyte antigens (HLA) are known to increase susceptibility to FT1D during pregnancy [3]. However, the association between FT1D in pregnancy and specific viral infections has not been reported.

We report the case of a patient who developed FT1D in pregnancy accompanied by Coxsackievirus B1 infection.

Case presentation

Our patient was a 31-year-old Japanese woman, gravida 1, para 1. She had no remarkable medical history, and there were no abnormalities during her medical examination. Her father and uncle had type 2 diabetes requiring insulin therapy. However, her sister did not have diabetes. The weight gain during her first 3 months of pregnancy was 1.1 kg. A regular examination at 29 weeks and 5 days was normal; her blood glucose level was 73 mg/dL, with negative levels of urinary glucose, and 3+ urinary ketone bodies.

At 30 weeks and 6 days, she was admitted with marked fatigue and dyspnea. However, she did not present with fever, headache, costochondritis, pharyngitis, diarrhea, maculopapular non-pruritic rash, nausea, or flu-like symptoms such as a sore throat, cough, or rhinorrhea.

On admission, she was alert. A physical examination revealed the following: temperature (T), 36.7 °C; pulse rate (P), 94 beats per minute (bpm); respiratory rate (R), 18/minute; and blood pressure (BP), 121/65 mmHg; fetal bradycardia was also observed, for which emergency cesarean section was performed, but the child was stillborn. The laboratory findings revealed diabetic ketoacidosis (DKA), with random sample glucose of 427 mg/dL, C-peptide reactivity (CPR) of 0.04 ng/mL, arterial pH of 6.91, bicarbonate of 6.7 mEq/L, and 3+ urinary ketone bodies. Despite the presence of DKA, the glycated hemoglobin (HbA1c) value was within the normal range (6.2%), and urinary CPR was extremely low at 0.5 μg/day. In addition, the serum elastase-1 and lipase levels were increased to 1939 (< 300) ng/dL and 119 (11–53) U/L, respectively. Antibody level against glutamic acid decarboxylase was 1.2 (< 1.5) U/mL. Neither anti-insulin nor anti-insulinoma-associated antigen-2 antibodies were detected. HLA II haplotypes showed DR8,12/DQ7,4. These results were indicative of a FT1D diagnosis (Table 1).

Table 1.

Laboratory data on admission

Hematology				ABGA (O2 5 L/m)
WBC	14,400 /μl	CRP	6.4 mg/dl	pH	6.91
neu.	74%	Amylase	139 IU/L	pCO2	33.7 mmHg
lym.	22%	Elastase1	1939 ng/dl	PO2	184 mmHg
mon.	3%	Lipase	119 U/L	HCO3−	6.5 mmol/L
eosino.	1%	Na	129 mEq/l	BE	−26.1 mmol/L
RBC	468 × 104 /μl	K	6.7 mEq/l
Hb	13.5 g/dl	Cl	95 mEq/l	Urine analysis
Ht	40.7%	Glu	427 mg/dl	pH	5.0
Plt	47.8 × 104 /μl	HbA1c	6.2%	Protein	(2+)
		Serum C-peptide	0.04 ng/ml	Glucose	(4+)
Chemistry		TSH	2.14 μIU/ml	Blood	(1+)
AST	14 IU/L	F-T4	1.03 ng/ml	Ketone	(4+)
ALT	12 IU/L			Urine C-peptide	0.5 μg/day
γ-GTP	12 IU/L
T-Bil	0.5 mg/dl	Coagulation		Autoantibodies
ALP	328 IU/l	PT	12.3 sec	GAD Ab	< 5.0 U/ml
TP	9 mg/dl	APTT	30.9 sec	IA-2 Ab	(−)
Alb	4.2 g/dl	FDP	8.47 μg/ml	Insulin Ab	< 0.4 U/ml
CK	29 IU/l	D-dimer	5.48 μg/ml
CRE	0.87 mg/dl			HLA haplotype
BUN	22 mg/dl			DR8, DR12, DQ7, DQ4

Ab antibody, ABGA arterial blood gas analysis, Alb albumin, ALP alkaline phosphatase, ALT alanine aminotransferase, APTT activated partial thromboplastin time, AST aspartate aminotransferase, BE base excess, BUN blood urea nitrogen, CK creatine kinase, CRE creatinine, CRP C-reactive protein, eosino. eosinophils, FDP fibrin degradation product, F-T4 free thyroxine, GAD glutamic acid decarboxylase, γ-GTP gamma-glutamyl transpeptidase, GLU glucose, Hb hemoglobin, HbA1c glycated hemoglobin, HCO₃⁻ bicarbonate, HLA human leukocyte antigens_, Ht hematocrit, lym. lymphocytes, mon. monocytes, neu. neutrophils, pCO₂ partial pressure of carbon dioxide, pO₂ partial pressure of oxygen, Plt platelets, PT prothrombin time, RBC red blood cells, T-Bil total bilirubin, TP total protein, TSH thyroid-stimulating hormone, WBC white blood cells

She was diagnosed as having DKA due to FT1D. She was simultaneously treated with fluid replacement and continuous insulin infusion to maintain vital signs, plasma glucose, and electrolyte levels. On day 2, ketonuria, electrolytes, and vital signs had normalized. On day 3, the continuous infusion of insulin was withdrawn, and daily multiple insulin injections were administered with blood glucose monitoring. On day 24, she continued to undergo treatment with multiple daily insulin injection therapy with insulin aspart (25 U/day) and insulin degludec (12 U/day).

Paired serum antiviral antibody test

To investigate the association between viral infection and FT1D, we performed serological testing for several viruses such as parainfluenza virus 1–3, Coxsackievirus A2–7, 9, 10, 16, B1–6, cytomegalovirus (CMV), Epstein–Barr virus (EBV), and human herpes virus (HHV) 6 at day 3, day 17, and day 38 (Table 2). A Coxsackievirus B1 antibody titer was significantly elevated from 1:32 to 1:256 (eightfold increase), whereas the other antibodies were not altered.

Table 2.

Viral antibodies

	Day 3	Day 17	Day 38		Day 3	Day 17
Parainfluenza1	< 10	< 10		Coxsackie B3	< 4	< 4
Parainfluenza2	< 10	< 10		Coxsackie B4	< 4	< 4
Parainfluenza3	160	160		Coxsackie B5	< 4	< 4
Coxsackie A2	< 4	< 4		Coxsackie B6	< 4	< 4
Coxsackie A3	8	8		CMV IgM	0.49	0.79
Coxsackie A4	16	16		CMV IgG	< 2	< 2
Coxsackie A5	< 4	< 4		EBV anti-VCA IgM	0	0.1
Coxsackie A6	< 4	< 4		EBV anti-VCA IgG	2.2	2.6
Coxsackie A7	8	4		EBV anti-EBNA IgG	3.1	3.3
Coxsackie A9	4	8		HHV-6 IgM	< 10	< 10
Coxsackie A10	< 4	< 4		HHV-6 IgG	160	160
Coxsackie A16	< 4	< 16		HHV-7 IgM	< 10	< 10
Coxsackie B1	32	64	256	HHV-7 IgG	40	40
Coxsackie B2	< 4	< 4

CMV cytomegalovirus, EBNA Epstein–Barr virus nuclear antigen, EBV Epstein–Barr virus, HHV human herpes virus, VCA viral capsid antigen

Discussion

FT1D is a special type of T1D that was first proposed by the Japanese scholar, Imagawa, in 2000 [1]. FT1D is characterized by rapid onset of DKA within a short time period, with normal to near-normal HbA1c levels at onset and complete β cell destruction [4]. A nationwide survey of FT1D in Japan revealed that it accounts for approximately 20% of cases of T1D [5]. The specific etiology and pathogenesis of FT1D are unclear and may be related to genetic predisposition, autoimmunity, viral infection, and pregnancy.

It is well known that the immunological milieu is significantly changed during pregnancy. However, the issue of whether the clinical and immunogenetic characteristics are different between the cases associated with and without pregnancy remains to be determined.

Although multiple genes have been implicated, HLA class II genes, especially the HLA-DR and DQ genes, are the most important. HLA class II genotypes DRB1*04:05- DQB1*04:01 strongly confer susceptibility to the development of FT1D [6]. In contrast, the frequency of DRB1*09:01-DQB1*03:03 tended to be higher in pregnant women with FT1D than in non-pregnant patients with FT1D [6]. The involvement of HLA class II haplotypes is suggested to vary depending on the presence or absence of pregnancy. In our pregnant patient, the HLA class II haplotypes were DR8,12/DQ7,4. To the best of our knowledge, these haplotypes have not been reported as conferring susceptibility to FT1D.

Viral infection is strongly associated with fulminant diabetes, as reported previously, and is evidenced by frequent flu-like symptoms, and it possibly has a seasonal variation in time of onset. Coxsackie B is a group of six types of EVs belonging to the Picornaviridae family. Coxsackie B viruses have a tropism for muscle cells and are most common in children but may occur in adults. Clinical manifestations include fever, aseptic meningitis, costochondritis, pharyngitis, myocarditis, diarrhea, and maculopapular non-pruritic rash [7].

Epidemiological studies have indicated an association between EVs and T1D. These viruses have a strong tropism for insulin-producing β cells; the destruction of these cells leads to T1D [8]. The exact mechanisms by which EVs could cause T1D are not known, but direct infection of β cells and virus-induced inflammation may play a role. Some studies have narrowed down the epidemiological association to a subset of EVs: group B Coxsackieviruses [9].

Recent studies have reported a variety of viral infections, including Coxsackievirus B1, B3, B4, A4, A5, A6, CMV, EBV, HHV6, 7, mumps, and parvovirus B19 to be involved in the development of FT1D [10–12]. However, the association between FT1D in pregnancy and certain viral infections has not been reported. Because HLA class II haplotypes with pregnancy and without pregnancy were different, we think it is possible that a different virus causes FT1D. However, our pregnant patient developed a Coxsackievirus B1 infection that manifested as fatigue and was involved in the development of FT1D.

Therefore, this case suggests that Coxsackievirus B infection is associated with FT1D with pregnancy and without pregnancy. DKA is a medical emergency during pregnancy and has high rates of fetal mortality. A prophylactic measure should be available to avoid the development of FT1D in pregnancy. Recent studies have narrowed down the epidemiological association to a subset of EVs: group B Coxsackieviruses; clinical development of a vaccine against T1D-associated EV types has been started [9]. A Coxsackievirus B vaccine may be protective against the development of FT1D in pregnancy.

Conclusion

We should assess pregnant women with symptoms of both fatigue and acute hyperglycemia for the presence of DKA, even if they are alert when presenting to the hospital. This case highlights that FT1D in pregnancy may be associated with Coxsackievirus B1 infection.

Abbreviations

CMV

Cytomegalovirus

CPR

C-peptide reactivity

DKA

Diabetic ketoacidosis

EBV

Epstein–Barr virus

EV

Enterovirus

FT1D

Fulminant type 1 diabetes

HbA1c

Glycated hemoglobin

HHV

Human herpes virus

HLA

Human leukocyte antigens

T1D

Type 1 diabetes

Authors’ contributions

TH and KH contributed to patient management. TH was a major contributor to the writing of the manuscript. YH, KY, HYa, TO, and TF critically reviewed the manuscript. All authors read and approved the final manuscript.

Funding

Nothing to declare.

Availability of data and materials

All data generated or analyzed during this study are included in this published article.

Ethics approval and consent to participate

This study was performed in accordance with the Declaration of Helsinki.

Consent for publication

Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.

Competing interests

The authors declare that they have no competing interests.