[Hypoglycemia due to antibodies to exogenous insulin in a patient with type 2 diabetes – a case report of treatment with new generation oral hypoglycemic agents].
Damian Ucieklak, Joanna Zięba-Parkitny, Elżbieta Kozek, Jan Skupień, Krystyna Sztefko, Maciej T Małecki
{"title":"[Hypoglycemia due to antibodies to exogenous insulin in a patient with type 2 diabetes – a case report of treatment with new generation oral hypoglycemic agents].","authors":"Damian Ucieklak, Joanna Zięba-Parkitny, Elżbieta Kozek, Jan Skupień, Krystyna Sztefko, Maciej T Małecki","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Hypoglycemic syndromes associated\nwith immune reactions against\ninsulin are rare phenomena described\npredominantly in Asians. Steroid\ntherapy, immunosuppression or plasmapheresis\nis often required.</p><p><strong>Case report: </strong>A 73-year-old White\nwoman with a 20-year history of type\n2 diabetes was admitted to hospital\ndue to recurrent incidents of hypoglycemia\nthat started several months\nafter insulin initiation (lispro 75/25)\nand increased in severity over the\nnext 5 years. They were accompanied\nby postprandial hyperglycemia up\nto 25 mmol/l. The patient’s glycated\nhemoglobin (HbA1c) was 70 mmol/\nmol (8.6%). During hypoglycemic\nepisodes recorded serum C-peptide\nwas 0.57-0.73 nmol/l (1.7-2.2 ng/ml),\nwhile insulin concentration exceeded\n7000 pmol/l (1000 mIU/l). Surreptitious\ninsulin administration was ruled out as\nwas, based on diagnostic imaging, the\npresence of an insulin secreting tumor.\nAnti-insulin antibody (AIA) level measured\nby 125I-insulin binding method was\n92.5% (normal < 8.2%). Hypoglycemic\nepisodes occurred for four days after\ndiscontinuation of insulin therapy\nand then resolved completely. Good\nglycemic control was maintained with\nmetformin, acarbose and dapagliflozin.\nThree months later dapagliflozin was\nreplaced with vildagliptine due to poor\ntolerance of a SGLT-2 inhibitor. Patient’s\nHbA1c was 54 mmol/mol (7.1%),\ntotal fasting insulin level 2577 pmol/l\nand AIA binding 85.9%. Over the next\nyear the patient has not experienced\nhypoglycemia and maintained good\nglycemic control, as HbA1c level was 53\nmmol/l (7.0%) and AIA binding 39.5%.</p><p><strong>Conclusions: </strong>In this rare case of\na patient with diabetes and hypoglycemic\nsyndrome related to AIA, we\nachieved a rapid and stable remission\nof hypoglycemia without immunosuppression.\nGood glycemic control, despite 20-year history\nof diabetes was achieved with oral hypoglycemic agents.</p>","PeriodicalId":21148,"journal":{"name":"Przeglad lekarski","volume":"74 1","pages":"41-3"},"PeriodicalIF":0.0000,"publicationDate":"2017-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Przeglad lekarski","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Hypoglycemic syndromes associated
with immune reactions against
insulin are rare phenomena described
predominantly in Asians. Steroid
therapy, immunosuppression or plasmapheresis
is often required.
Case report: A 73-year-old White
woman with a 20-year history of type
2 diabetes was admitted to hospital
due to recurrent incidents of hypoglycemia
that started several months
after insulin initiation (lispro 75/25)
and increased in severity over the
next 5 years. They were accompanied
by postprandial hyperglycemia up
to 25 mmol/l. The patient’s glycated
hemoglobin (HbA1c) was 70 mmol/
mol (8.6%). During hypoglycemic
episodes recorded serum C-peptide
was 0.57-0.73 nmol/l (1.7-2.2 ng/ml),
while insulin concentration exceeded
7000 pmol/l (1000 mIU/l). Surreptitious
insulin administration was ruled out as
was, based on diagnostic imaging, the
presence of an insulin secreting tumor.
Anti-insulin antibody (AIA) level measured
by 125I-insulin binding method was
92.5% (normal < 8.2%). Hypoglycemic
episodes occurred for four days after
discontinuation of insulin therapy
and then resolved completely. Good
glycemic control was maintained with
metformin, acarbose and dapagliflozin.
Three months later dapagliflozin was
replaced with vildagliptine due to poor
tolerance of a SGLT-2 inhibitor. Patient’s
HbA1c was 54 mmol/mol (7.1%),
total fasting insulin level 2577 pmol/l
and AIA binding 85.9%. Over the next
year the patient has not experienced
hypoglycemia and maintained good
glycemic control, as HbA1c level was 53
mmol/l (7.0%) and AIA binding 39.5%.
Conclusions: In this rare case of
a patient with diabetes and hypoglycemic
syndrome related to AIA, we
achieved a rapid and stable remission
of hypoglycemia without immunosuppression.
Good glycemic control, despite 20-year history
of diabetes was achieved with oral hypoglycemic agents.