Diagnosis and Treatment > Investigation > Exercise tolerance
You are looking at 1 - 3 of 3 items
Search for other papers by Marina Yukina in
Google Scholar
PubMed
Search for other papers by Nurana Nuralieva in
Google Scholar
PubMed
Search for other papers by Maksim Solovyev in
Google Scholar
PubMed
Russian Academy of Sciences, Endocrinology Service, Department of Therapeutic Endocrinology, Endocrinology Research Centre (ERC), Moscow, Russia
Search for other papers by Ekaterina Troshina in
Google Scholar
PubMed
Search for other papers by Evgeny Vasilyev in
Google Scholar
PubMed
Summary
Insulin autoimmune syndrome (Hirata’s disease) is a disorder caused by development of autoantibodies to insulin and manifested by hypoglycaemic syndrome. The overwhelming majority of physicians do not include it in the differential diagnosis of hypoglycaemic states because of a misconception of an extremely low prevalence of this condition. This results in unnecessary drug therapy and unjustified surgical interventions in patients that otherwise would be successfully treated conservatively. This disease is strongly associated with certain alleles of the HLA gene. In most cases, this condition develops in predisposed individuals taking drugs containing sulfhydryl groups. Formation of autoantibodies to insulin may be observed in patients with other autoimmune disorders, as well as in those with multiple myeloma or monoclonal gammopathy of undetermined significance. This paper presents the first Russian case report of insulin autoimmune syndrome in an adult patient.
Learning points:
-
Insulin autoimmune syndrome, Hirata’s disease, anti-insulin antibodies, and hypoglycaemia.
Search for other papers by Frank Gao in
Google Scholar
PubMed
Search for other papers by Stephen Hall in
Google Scholar
PubMed
Department of Medicine (Alfred), Monash University, Melbourne, Australia
Search for other papers by Leon A Bach in
Google Scholar
PubMed
Summary
Sodium/glucose co-transporter 2 (SGLT2) inhibitors are novel oral hypoglycaemic agents that are increasingly used in the management of type 2 diabetes mellitus (T2DM). They are now recommended as second-line pharmacotherapy (in conjunction with metformin) in patients with type 2 diabetes and established atherosclerotic heart disease, heart failure or chronic kidney disease due to their favourable effects on cardiovascular and renal outcomes. We report a case of a 69-year-old man who developed muscle pain, weakness and wasting after commencing the SGLT2 inhibitor empagliflozin. This persisted for 1 year before he underwent resistance testing, which confirmed muscle weakness. His symptoms resolved within weeks of ceasing empagliflozin, with improvement in muscle strength on clinical assessment and resistance testing and reversal of MRI changes. No other cause of myopathy was identified clinically, on biochemical assessment or imaging, suggesting that empagliflozin was the cause of his myopathy.
Learning points:
-
Empagliflozin, a commonly used SGLT2 inhibitor, was associated with myopathy.
-
A high degree of suspicion is required to diagnose drug-induced myopathy, with a temporal relationship between starting the medication and symptom onset being the main indicator.
-
Recognition of drug-induced myopathy is essential, as discontinuation of the offending drug typically improves symptoms.
Schools of Medicine and Public Health
Search for other papers by Christopher W Rowe in
Google Scholar
PubMed
Search for other papers by Kirsten Murray in
Google Scholar
PubMed
Search for other papers by Andrew Woods in
Google Scholar
PubMed
Health Sciences, University of Newcastle, Newcastle, New South Wales, Australia
Search for other papers by Sandeep Gupta in
Google Scholar
PubMed
Schools of Medicine and Public Health
Search for other papers by Roger Smith in
Google Scholar
PubMed
Schools of Medicine and Public Health
Search for other papers by Katie Wynne in
Google Scholar
PubMed
Metastatic thyroid cancer is an uncommon condition to be present at the time of pregnancy, but presents a challenging paradigm of care. Clinicians must balance the competing interests of long-term maternal health, best achieved by iatrogenic hyperthyroidism, regular radioiodine therapy and avoidance of dietary iodine, against the priority to care for the developing foetus, with inevitable compromise. Additionally, epidemiological and cellular data support the role of oestrogen as a growth factor for benign and malignant thyrocytes, although communicating the magnitude of this risk to patients and caregivers, as well as the uncertain impact of any pregnancy on long-term prognosis, remains challenging. Evidence to support treatment decisions in this uncommon situation is presented in the context of a case of a pregnant teenager with known metastatic papillary thyroid cancer and recent radioiodine therapy.
Learning points:
-
Pregnancy is associated with the growth of thyroid nodules due to stimulation from oestrogen receptors on thyrocytes and HCG cross-stimulation of the TSH receptor.
-
Thyroid cancer diagnosed during pregnancy has not been shown to be associated with increased rates of persistent or recurrent disease in most studies.
-
There is little evidence to guide the management of metastatic thyroid cancer in pregnancy, where both maternal and foetal wellbeing must be carefully balanced.