1/13
Why doesn't hemolysis cause acute kidney injury as easily as rhabdomyolysis?

I see a lot of hemolysis and can't think of a case of AKI that resulted.

Rhabdo? I immediately worry about AKI.

If heme is the toxic molecule, shouldn't both conditions be equally nephrotoxic?
2/
🔑Heme is contained in both hemoglobin and myoglobin and is the toxic molecule in BOTH hemolysis and rhabdomyolysis.

The mechanism of heme toxicity won't be covered in this thread. Instead, we'll stick with why rhabdo causes more AKI.

pubmed.ncbi.nlm.nih.gov/31018590/
3/
Before moving on, it is important to note that hemolysis CAN cause AKI.

Historically, massive hemolysis from ABO mismatch was a major cause. Now the causes are more varied.

pubmed.ncbi.nlm.nih.gov/31668630/
4/
One explanation for the difference: haptoglobin (HPG) binding to free hemoglobin (HGB)

Haptoglobin exists to protect us from free hemoglobin.

Given the large size of HGB:HPG complexes, they are not filtered by the kidney and won't injure tubules.

pubmed.ncbi.nlm.nih.gov/31455889/
5/
But we've all cared for patients with undetectable haptoglobin. That's one way we diagnose hemolysis!

So, while haptoglobin is one mode of protection, it can easily be exhausted.

There must be more to the difference between hemolysis and rhadbo.

pubmed.ncbi.nlm.nih.gov/7365971/
6/
The other difference: hemoglobin (a tetramer) is larger than myoglobin (a monomer).

• Hemoglobin: 68 kd
• Myoglobgin 17 kd

🔑Myoglobin is more freely filtered by the glomerulus.

This gives its heme molecular access to the tubules with resulting injury.
7/
Interim Summary: Although both myoglobin and HGB contain toxic heme, rhabdo is more likely than hemolysis to cause AKI.

Explanations:
🔑Haptoglobin binds HGB
🔑HGB is larger and less freely filtered

Result: much higher serum levels of HGB are required to cause AKI!
8/
In fact, notice that hemoglobin is basically the same size as albumin.

• Hemoglobin: 68 kd
• Albumin: 69 kd

Maybe its large size doesn't permit ANY glomerular filtration.

But this can't be. As noted above, hemolysis CAN lead to pigment nephropathy.
9/
In 1965, Szabó et al confirmed that hemoglobin DOES pass across the glomerulus and into renal tubules.

So, now we have another mystery.

How does hemoglobin - a molecule that is the same size as albumin - cross glomerular capillaries and cause injury?

pubmed.ncbi.nlm.nih.gov/5859188/
10/
In 1969, Bunn et al provided an answer.

Observing that hemoglobin exists not just as tetramers but also as DIMERS, they wondered whether these smaller dimers were making their way into the urine, causing AKI.

pubmed.ncbi.nlm.nih.gov/5778789/
11/
Attaching hemoglobin to bis (N-maleimidomethyl) ether (BME) makes it unable to dissociate to dimers.

Using BME, Bunn et al showed that dimers undergo more renal excretion, as compared with tetramers.

🔑Dimers are what get filtered and cause injury!

pubmed.ncbi.nlm.nih.gov/5778789/
12/
There are other contributors to the difference in rates of AKI between rhabdo and hemolysis.

One example: Rhabdomyolysis patients have more volume depletion, which is itself a risk factor for AKI.
13/13
⚡️Why doesn't hemolysis cause AKI as easily as rhabdomyolysis?

🔹Haptoglobin binds HGB
🔹HGB is larger than myoglobin
🔹HGB dissociates into dimers which can be filtered

Result: HGB isn't filtered as well as myoglobin (less injury) but HGB dimers can be and do cause AKI!

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More from @tony_breu

31 Mar
1/9
Great question!

From what I gather, the exact explanation for the low alkaline phosphatase in Wilson's disease remains unexplained.
2/
The first description of the association between low AP and Wilson's came in a 1986 paper by Shaver, Bhatt, and Combes.

pubmed.ncbi.nlm.nih.gov/3758940/
3/
They describe patients with acute hemolytic anemia in the setting of Wilson's disease who are noted to have low AP.

They wonder whether the acute increase in serum copper may compete with zinc for incorporation into AP.

pubmed.ncbi.nlm.nih.gov/3758940/
Read 9 tweets
28 Mar
1/11
Why is alkaline phosphatase elevated in biliary obstruction?

This question was debated for decades. The current explanation is NOT what I had expected.

Will you be surprised too?
2/
Let's start with a question.

What explanation have you heard for the increased alkaline phosphatase (AP) in biliary obstruction?
3/
One potential explanation is that AP leaks into the blood when hepatocytes are injured.

The problem: AP isn't markedly elevated in conditions with marked acute liver injury. For example, AP is only mildly elevated in acute viral hepatitis.

bit.ly/39kxaom
Read 11 tweets
21 Mar
1/12
Why do we use ACE inhibitors in scleroderma renal crisis?

I learned this early in training but never understood why these drugs were so game-changing.

Let's have a look.
2/
To start, a few key features of scleroderma renal crisis (SRC). Most patients present with:

• Abrupt onset of hypertension
• Oliguric acute kidney injury
• Normal urinalysis

Up to 50% have signs of microangiopathic hemolytic anemia.

pubmed.ncbi.nlm.nih.gov/27641135/
3/
Decades ago, the mortality for scleroderma involving the kidney was high with SRC considered universally fatal.

Things began to change in the 1970s.

pubmed.ncbi.nlm.nih.gov/4587746/
Read 12 tweets
13 Mar
1/14
How does fever help us fight infections?

For millennia, fever has been recognized as a beneficial response to invading pathogens.

If this is so, why don't we have a resting temperature of 102°F (38.9°C)? Wouldn't that protect us even better?

Let's have a look.
2/
Fever emerged approximately 600 million years ago and is conserved in vertebrates. This suggests its benefit.

As you'll see in the next tweet, even ectothermic (cold-blooded) vertebrates demonstrate a "febrile" response.

pubmed.ncbi.nlm.nih.gov/24692136/
3/
In a 1975 study, ectothermic lizards were infected with A. hydrophila and placed in environments at varying temperatures.

😀75% survived at 42°C (107.6°F)
😕25% survived at 38°C (100.4°F)
🥴0% survived at 34°C (93.2°F)

🔑↑temperatures = ↑survival

pubmed.ncbi.nlm.nih.gov/1114347/
Read 18 tweets
27 Jan
1/14
Why is cerebrospinal fluid (CSF) glucose low in bacterial meningitis?

Before we review potential mechanisms, I'm interested in the explanation you've heard/used.

What do you think causes low CSF glucose (hypoglycorrhachia)?
2/
First, let's examine the most common causes of hypoglycorrhachia.

☞ While bacterial meningitis is the single most common cause, it accounts for fewer than a quarter of cases.

We'll come back to this.

pubmed.ncbi.nlm.nih.gov/24326618/
pubmed.ncbi.nlm.nih.gov/26299186/ Image
3/
Now to the potential mechanisms. A number of hypotheses have been offered to explain hypoglycorrhachia.

🔹Bacterial consumption of glucose
🔹WBC consumption
🔹Brain consumption
🔹Decreased entry into CSF

...and others

Let's examine these.
Read 14 tweets
30 Dec 20
1/16
Why do B12 and folate deficiencies lead to HUGE red blood cells?

And, if the issue is DNA synthesis, why are red blood cells (which don't have DNA) the key cell line affected?

For answers, we'll have to go back a few billion years.
2/
RNA came first. Then, ~3-4 billion years ago, DNA emerged.

Among their differences:
🔹RNA contains uracil
🔹DNA contains thymine

But why does DNA contains thymine (T) instead of uracil (U)?

pubmed.ncbi.nlm.nih.gov/12110897/
3/
🔑Cytosine (C) can undergo spontaneous deamination to uracil (U).

In the RNA world, this meant that U could appear intensionally or unintentionally. This is clearly problematic. How can you repair RNA when you can't tell if something is an error?

pubmed.ncbi.nlm.nih.gov/18837522/
Read 16 tweets

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