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How should individuals with positive autoimmune T1D autoantibodies be monitored over time?

How should individuals with positive autoimmune T1D autoantibodies be monitored over time?

Individuals who screen positive for ≥1 autoimmune islet cell antibodies need periodic medical monitoring, which includes regular assessments of blood glucose and HbA1c levels. You can also educate them about symptoms of diabetes, diabetic ketoacidosis (DKA), and provide psychosocial support to prepare them for a possible clinical diagnosis for type 1 diabetes (T1D).1

Can autoimmune type 1 diabetes be detected years before symptom onset?

Can autoimmune type 1 diabetes be detected years before symptom onset?

Autoimmune type 1 diabetes (T1D) is a progressive disease in which the decline in beta cell function usually begins months or sometimes years before clinical symptoms are observed.1–3 You can identify such patients at risk of developing autoimmune T1D before clinical symptoms are noticed by you or your patient.3

Autoimmune Type 1 Diabetes

Autoimmune Type 1 Diabetes

The Type 1 Diabetes (T1D) field is evolving.

Recognition of the presymptomatic stages in T1D is growing.1-4 

The clinical benefits of early detection of T1D are being highlighted.3-4 Programmes focusing on early detection through testing and screening for presymptomatic autoimmune T1D are increasingly offered to risk populations and the general population.1,2

Why choose PRALUENT<sup>®</sup>?

Why choose PRALUENT®?

The usual starting dose for PRALUENT is 75 mg administered subcutaneously once every 2 weeks. Patients requiring larger LDL-C reduction (>60%) may be started on 150 mg once every 2 weeks, or 300 mg once every 4 weeks (monthly), administered subcutaneously.2

How to use PRALUENT<sup>®</sup>?

PRALUENT is available as a unique,¥ once-monthly pen

Prevent the Event

Prevent the Event

Despite major advances in our understanding of atherosclerosis, ASCVD remains the leading cause of death globally.1

Why Choose Toujeo<sup>®</sup> (Insulin Glargine)

Why Choose Toujeo® (Insulin Glargine)

Fabry disease

Fabry disease

Fabry disease is an X-linked lysosomal storage disease due to a defect in the gene encoding the lysosomal enzyme alpha-galactosidase A (α-Gal A), causing progressive cellular accumulation of the substrate globotriaosylceramide (GL-3) and globo-triaosylsphingosine (lyso-GL-3).

How to diagnose Fabry

How to diagnose Fabry

Think Fabry, think timely testing first.

Monitoring disease progression

Monitoring disease progression

Think Fabry, think regular profile-based assessments.

Cardiac involvement in Fabry disease

Cardiac involvement in Fabry disease

Cardiovascular disease is the leading cause of death in Fabry disease patients.1 Undiagnosed and untreated Fabry disease leads to progressive, irreversible, life-threatening heart injury.2,3

Renal involvement in Fabry disease

Renal involvement in Fabry disease

Think Fabry, think renal involvement that may present early in life and could go undetected.