Friday, November 14, 2025

Meet Type 1.5 Diabetes—the Overlooked Condition More Common in People Over 30

 Receiving a diabetes diagnosis can be bittersweet. You may feel anxious and scared about what lies ahead and relieved knowing you’ll be connected with the right treatment. But what if the diagnosis isn’t spot on and the treatment doesn’t seem to be helping you in the long term? That’s what can happen for people with type 1.5 diabetes—a form of diabetes that’s sometimes overlooked or misidentified.

Clinically known as latent autoimmune diabetes in adults (LADA), this condition often looks a lot like type 2 diabetes, especially in its earlier stages. But in reality, it’s an autoimmune disease that eventually requires insulin, just like type 1 diabetes.

Because LADA usually appears in adulthood and develops gradually, many people with the condition are misdiagnosed with type 2 diabetes, which is a big problem that can delay the right treatment. Oral medications and lifestyle changes like diet and exercise that are typically prescribed to treat type 2 diabetes may not bring the improvements doctors expect to see, all the while the immune system continues to gradually attack cells in the pancreas that produce insulin. As a result, blood sugar isn’t in control and the body undergoes further harm.

 Different types of diabetes require different treatment approaches, so getting the right diagnosis matters. Here’s what you should know about this condition, how it impacts the body, and why a proper diagnosis is so important.

How is LADA different from other types of diabetes?

To understand LADA, it’s helpful to understand how type 1 and type 2 diabetes work.

Type 1 diabetes is an autoimmune condition where the pancreas either makes very little insulin or no insulin because the immune system attacks important cells in the pancreas that produce insulin. Without insulin, blood sugar builds up in the bloodstream, often causing sharp spikes in blood sugar. People with this form of diabetes have to take insulin each day to survive. It can happen at any age, but typically develops in children or young adults.

“It’s an autoimmune condition where you have antibodies that attack the pancreatic beta cells— the cells that make insulin—and they destroy those cells,” Rozalina McCoy, MD, associate division chief for clinical research, Division of Endocrinology, Diabetes, and Nutrition at the University of Maryland School of Medicine tells SELF. “That is what causes insulin deficiency.”

Type 2 diabetes is a chronic condition where the body still produces insulin, but has trouble using it properly—this is known as insulin resistance and causes high blood sugar. “If your insulin doesn’t work as well, the glucose can’t get from the blood into the cells as efficiently, so blood sugar rises,” Dr. McCoy says. “This pathway is what leads to type 2 diabetes.”

Type 2 is way more common than type 1 diabetes and accounts for between 90% and 95% of people with diabetes. Some of the most common risk factors include having overweight, being physically active fewer than three times per week, being 45 or older, or having an immediate family member with the condition. Type 2 diabetes is usually managed with lifestyle changes and oral medications like Metformin that address the underlying insulin resistance, though some people eventually need insulin.

So where does LADA fit in?

LADA is sometimes called type 1.5 diabetes because it shares features of both type 1 and type 2 diabetes. Similar to type 1 diabetes, LADA is an autoimmune condition where your immune system mistakenly attacks important cells in the pancreas that produce insulin. But while type 1 diabetes usually appears suddenly in kids or young adults, LADA develops more gradually and is typically diagnosed in people who are 30 or older.

In the early stages, people with LADA are able to make enough insulin to keep their blood sugar levels somewhat close to a normal range. This is where things can get a bit complicated. Because the body is still producing insulin in the early stages of LADA for at least six months following diagnosis, people with this condition are often misdiagnosed with type 2 diabetes and prescribed oral medications like metformin and lifestyle changes.

That’s a big problem, because when someone has LADA, their body’s ability to produce insulin declines, and over time, those medications stop working.

“They ultimately, at some point, progress to needing insulin, just like type 1,” Dr. McCoy says. “But it happens in adulthood and it's latent, meaning it's slower.”

If someone with LADA is misdiagnosed with type 2 diabetes, they don’t know they need insulin and are instead left taking medications and trying lifestyle changes that don’t actually address the issues going on in their body. This could result in uncontrolled high blood sugar, which can increase the risk for strokes, heart attacks, ketoacidosis (a life-threatening diabetes complication), and other serious issues, Wilson Sze, MD, an endocrinologist at Houston Methodist, tells SELF.

“If you don’t produce enough insulin yourself, having uncontrolled diabetes and having persistently high blood sugars can really cause a lot of issues,” Dr. Sze says.

Usually, LADA is classified as a form of type 1 diabetes.

Because LADA is an autoimmune condition that requires insulin therapy, many physicians actually view it as a subset of type 1 diabetes rather than as a completely separate type of diabetes. Dr. McCoy is among them, explaining that LADA is simply type 1 diabetes in adults that take longer to develop a need for insulin therapy.

“The more we test for this in adults, the more we understand about the fact that type 1 diabetes is a heterogeneous disease—it's not the same in everybody,” Dr. McCoy says. “Across all ages there's variability in how long the period is from getting antibodies to those antibodies destroying the pancreatic cells and developing diabetes.”

A proper diagnosis is key in connecting people with the right treatment.

A type 2 diabetes diagnosis when someone actually has LADA can get in the way of proper treatment. Dr. Sze says that when people are in this scenario, they may go to their doctor saying that they’ve been working hard to do everything their doctor suggested to treat type 2 diabetes—like exercising more, eating a more nutritious diet, and taking prescribed oral medications—but they’re just not seeing results. To him, that’s a sign he should consider screening for LADA. “It's very easy for us to screen for type one or LADA,” he says. “It's just a blood test.”

To diagnose the condition, doctors typically start with fasting blood sugar, A1C, and glucose tolerance tests, all of which measure blood sugar levels and help confirm diabetes or prediabetes. Doctors also need to confirm the autoimmune response, which is evident through the presence of those autoantibodies that attack cells in the pancreas that we mentioned earlier.

Your endocrinologist will likely order blood tests that look for diabetes-related autoantibodies and they’ll also measure C-peptide levels, which indicate how much insulin the body is still making. If test results show low C-peptide levels and the presence of antibodies, there’s a good chance someone has LADA, not type 2 diabetes, Dr. Sze says.

“That's an indication that it's time to think outside the box and switch from oral medications or oral hypoglycemics to insulin therapy,” Dr. Sze says.

Signs to look out for

LADA can be easy to overlook because it develops later than life and often presents with the same signs as type 2 diabetes, including:

  • increased thirst
  • peeing more than usual
  • weight loss seemingly for no reason
  • feeling fatigued and tired
  • blurry vision
  • numbness or tingling in your hands and feet

Dr. Sze and Dr. McCoy also look for some other telling signs: someone with LADA may have a family history of type 1 diabetes, a BMI that’s a bit lower than typically seen in patients with type 2 diabetes, and they may have uncontrolled blood sugar even though they’re working really hard on diet and lifestyle changes and taking oral medication for type 2 diabetes. These signs let the physician know that someone may have an autoimmune condition where the pancreas simply isn’t making enough insulin, Dr. Sze says.

“If somebody's presentation and history aren't consistent with type two diabetes, they should be checked for type one diabetes or LADA, because the treatments are so different,” Dr. McCoy says.

Treatment can help avoid or delay complications.

The exact approach to treating LADA varies depending when someone is diagnosed and how far along they are in the condition’s progression at that point. Your doctor may prescribe oral medication and lifestyle changes like physical activity and healthy eating if the pancreas is still producing insulin. But eventually, as the body’s ability to produce insulin declines, insulin therapy will be needed. The timeline can vary, but sometimes this takes years, Dr. McCoy says.

As the condition progresses, it’s important that your doctor monitors you regularly to determine when treatment with insulin is necessary. “At some point people with LADA will need insulin and we don't want to miss that,” Dr. McCoy adds.

 

This is only for your information, kindly take the advice of your doctor for medicines, exercises and so on.   

 

 

 

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Sunday, January 19, 2020

Genetic signature helps distinguish latent autoimmune diabetes in adults from pediatric-onset T1D

A multi-center team of researchers led by Children's Hospital of Philadelphia (CHOP) has discovered a genetic signature that could help distinguish an adult-onset form of diabetes sharing many type 1 diabetes (T1D) characteristics from pediatric-onset T1D, opening the door to potentially more straightforward diagnostic tests for the adult condition and improving responses by ensuring patients receive the most appropriate treatment.

This is our first insight into genetic differences between latent autoimmune diabetes in adults and T1D in children that may be diagnostically useful. We have found a genetic means of discriminating between the two conditions without expensive and cumbersome anti-autobody screening."Struan Grant, PhD, study leader, Co-Director of the Center for Spatial and Functional Genomics at CHOP and the Daniel B. Burke Endowed Chair for Diabetes Research
The study was published online December 16, 2019 in Diabetes Care.

Latent autoimmune diabetes in adults (LADA) is sometimes referred to as "type 1.5 diabetes" because it shares characteristics of both T1D and type 2 diabetes (T2D). Like T1D, LADA produces autoantibodies that attack the body's insulin-producing beta cells in the pancreas. However, like those with T2D, patients with LADA are diagnosed in adulthood and do not require insulin at the time of diagnosis. For this reason, LADA is often misdiagnosed as T2D; studies have shown that up to 10% of T2D diagnoses are, in fact, LADA, and as a result patients do not respond to the commonly inappropriate treatments prescribed to them.

An earlier genome-wide association study led by CHOP found that, from a genetic perspective, LADA has more in common with T1D than with T2D. Researchers wanted to take a deeper dive and look for genetic differences that could help discriminate between LADA and T1D, meaning the diagnosis of LADA could potentially begin with a simple genotype array, rather than with a more complex and expensive auto-antibody screening.

To do so, the team decided to look at the major histocompatibility complex (MHC), a highly variable region of the genome that helps drive the immune system and is implicated in T1D. Earlier studies have shown that when researchers control for T1D genetic variants in one part of the MHC, other variants associated with T1D appear in another part of the MHC.

The study team applied that methodology to both a set of T1D data as well as a cohort of LADA patients. They found that when it came to the T1D group, the results from the earlier studies held: controlling for genetic variants in one part of the MHC revealed variants in another part of the MHC.
However, researchers did not find the same effect with LADA patients. When controlling for genetic variants in the MHC in those patients, the additional association was not observed within this key region - an important genetic distinction between the two conditions. When a sensitivity test was applied to the two cohorts, researchers still saw the effect only in T1D patients, not in those with LADA.

"This suggests that these MHC class associations may be a genetic discriminator between LADA and childhood-onset T1D," said Diana Cousminer, PhD, a geneticist at CHOP and a joint-first author of the study. "The next step is to look at this association in different ethnicities, particularly African ancestry, where the prevalence of adult-onset diabetes can be significantly higher in certain parts of the world."

This is only for your information, kindly take the advice of your doctor for medicines, exercises and so on.     
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https://gseasyrecipes.blogspot.com. feel free to view for easy, simple and healthy recipes    
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Thursday, January 16, 2020

Genetic signature helps distinguish latent autoimmune diabetes in adults from pediatric-onset T1D

A multi-center team of researchers led by Children's Hospital of Philadelphia (CHOP) has discovered a genetic signature that could help distinguish an adult-onset form of diabetes sharing many type 1 diabetes (T1D) characteristics from pediatric-onset T1D, opening the door to potentially more straightforward diagnostic tests for the adult condition and improving responses by ensuring patients receive the most appropriate treatment.

This is our first insight into genetic differences between latent autoimmune diabetes in adults and T1D in children that may be diagnostically useful. We have found a genetic means of discriminating between the two conditions without expensive and cumbersome anti-autobody screening."

Latent autoimmune diabetes in adults (LADA) is sometimes referred to as "type 1.5 diabetes" because it shares characteristics of both T1D and type 2 diabetes (T2D). Like T1D, LADA produces autoantibodies that attack the body's insulin-producing beta cells in the pancreas. However, like those with T2D, patients with LADA are diagnosed in adulthood and do not require insulin at the time of diagnosis. For this reason, LADA is often misdiagnosed as T2D; studies have shown that up to 10% of T2D diagnoses are, in fact, LADA, and as a result patients do not respond to the commonly inappropriate treatments prescribed to them.

An earlier genome-wide association study led by CHOP found that, from a genetic perspective, LADA has more in common with T1D than with T2D. Researchers wanted to take a deeper dive and look for genetic differences that could help discriminate between LADA and T1D, meaning the diagnosis of LADA could potentially begin with a simple genotype array, rather than with a more complex and expensive auto-antibody screening.

To do so, the team decided to look at the major histocompatibility complex (MHC), a highly variable region of the genome that helps drive the immune system and is implicated in T1D. Earlier studies have shown that when researchers control for T1D genetic variants in one part of the MHC, other variants associated with T1D appear in another part of the MHC.

The study team applied that methodology to both a set of T1D data as well as a cohort of LADA patients. They found that when it came to the T1D group, the results from the earlier studies held: controlling for genetic variants in one part of the MHC revealed variants in another part of the MHC.

However, researchers did not find the same effect with LADA patients. When controlling for genetic variants in the MHC in those patients, the additional association was not observed within this key region - an important genetic distinction between the two conditions. When a sensitivity test was applied to the two cohorts, researchers still saw the effect only in T1D patients, not in those with LADA.

"This suggests that these MHC class associations may be a genetic discriminator between LADA and childhood-onset T1D," said Diana Cousminer, PhD, a geneticist at CHOP and a joint-first author of the study. "The next step is to look at this association in different ethnicities, particularly African ancestry, where the prevalence of adult-onset diabetes can be significantly higher in certain parts of the world."

This is only for your information, kindly take the advice of your doctor for medicines, exercises and so on.     
https://gscrochetdesigns.blogspot.com. one can see my crochet creations  
https://gseasyrecipes.blogspot.com. feel free to view for easy, simple and healthy recipes    
https://kneereplacement-stickclub.blogspot.com. for info on knee replacement
 

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Saturday, September 16, 2017

WHAT HAPPENS IN YOUR BODAY WHEN YOU EAT TOO MUCH SALT

Your body needs salt for fluid balance, muscle and nerve function. But salt can wreak havoc on your body when you take too much of it.

Who would have thought that salt could also affect your brain function? Studies have indicated that low levels of sodium could impair memory. However, a  study found that adults who lead sedentary lifestyles and consume high-sodium diets had a higher chance of cognitive decline than those with less salt in their diets.

High blood pressure

Most of the sodium in the diet comes from salt, although many foods contain small amount of sodium. Sodium is both an electrolyte and mineral. It helps keep the water and electrolyte balance of the body. But too much sodium in your system causes your body to hold onto water, putting an extra burden on your heart and blood vessels. Too much salt or too much water in your system will affect the balance and may lead to or raise blood pressure in some people. Having less sodium in diet may help you lower or avoid high blood pressure.

Heart disease and stroke

High blood pressure caused by eating too much salt can damage the arteries leading to the heart. Researchers found that high intake of salt may double your risk of heart failure. High salt consumption is one of the major causes of high blood pressure and an independent risk factor for cardiovascular disease and stroke.

Kidney problems

Your kidneys remove wastes and extra water from the blood through urine. A high salt diet will raise the amount of sodium in your bloodstream and wreck the delicate balance, affecting the ability of your kidneys to remove water and resulting in higher blood pressure. A high salt intake has also been linked to high amount of protein in the urine, which is a major risk factor for the decline of kidney function.

Diabetes

A new research being presented at this year's annual meeting of the Study suggests that sodium intake may be linked to an increased risk of developing both type 2 diabetes (T2D) and Latent Autoimmune Diabetes in Adults (LADA).
LADA is a form of type 1 diabetes in which the insulin-producing cells in the pancreas are destroyed by the body's own immune system. But unlike typical type 1 diabetes, LADA develops very slowly, sometimes over a period of years.

How much sodium should you eat a day?

Many people consume a lot of sodium without realising the consequences of it. The American Heart Association recommends no more than 2,300 milligrams (mgs) - amounts to one teaspoon - per day and an ideal limit of no more than 1,500 mg per day for most adults.
According to the World health organisation (WHO), children should not eat more than 4grams of salt a day - babies under a year need less than 1g of salt per day as their kidneys can’t cope with sodium.
Avoiding or cutting back on prepackaged and processed foods can help reduce your risk of serious diseases.

THIS IS ONLY FOR INFORMATION, ALWAYS CONSULT YOU PHYSICIAN BEFORE HAVING ANY PARTICULAR FOOD/ MEDICATION/EXERCISE/OTHER REMEDIES.
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