1/13
Why does adrenal insufficiency (particularly adrenal crisis) lead to hypotension?

I don't think of glucocorticoids as "pressors" and yet when they're lacking patients are at great risk for shock.

Let's have a look.
2/
Hypotension has long been associated with adrenal insufficiency.

For example, one report of 108 cases of Addison's Disease (i.e., primary adrenal insufficiency) found that:

⚡️88% of patients presented with hypotension

PDF: t.ly/aDzv
3/
In primary adrenal insufficiency (PAI), hypotension is partly due to volume depletion related to mineralocorticoid deficiency.

But even in PAI the hemodynamic profile isn't simply ↓cardiac output from ↓venous return (i.e., volume depletion).

PDF: t.ly/Ooej
4/
And patients with secondary adrenal insufficiency aren't lacking in mineralocorticoids and still experience adrenal crisis.

Something else is going on in both primary and secondary adrenal insufficiency leading to hypotension.

PDF: t.ly/qmnLf
5/
Although there are many phenotypes of hypotension in adrenal insufficiency, distributive shock with decreased systemic vascular resistance is common.

This is just one case report, of many. Tweet 3 shows other examples.

PDF: t.ly/PsCd
6/
One key observation:

🔑 Patients with adrenal insufficiency have LOW levels of epinephrine.

And this is despite intact catecholamine-producing chromaffin cells. It appears cortisol plays a role in epinephrine homeostasis.

PDF: t.ly/5qGp
7/
To understand how cortisol ensures adequate epinephrine levels we must review catecholamine synthesis.

Nearly all epinephrine is synthesized within the adrenals from norepinephrine by the enzyme phenylethanolamine N-methyltransferase (PNMT).

PDF: t.ly/fybH
8/
Early experiments demonstrated that PNMT levels fall after hypophysectomy and dexamethasone restores the lost activity.

🔑Conclusion: generation of epinephrine is regulated by glucocorticoids!

PDF: t.ly/DV1n
9/
As with other foci, glucocorticoids stimulate the gene expression of PNMT.

In one study dexamethasone increased PNMT gene transcription 2.3-fold.

PDF: t.ly/NBvJ
10/
There are other explanations for why adrenal insufficiency (AI) leads to hypotension. For example:

🔑Dexamethasone leads to increased expression of α1 receptors

This may partly explain why AI commonly presents with distributive shock.

PDF: t.ly/pnpZ
11/
Glucocorticoids also:

↓ COMT and MAO leading to ↓ epinephrine degradation
↑ β receptors leading to enhanced sensitivity to catecholamines

Etc.

In short: they do A LOT.

PDF: t.ly/QqqE
12/
The interaction between glucocorticoids and catecholamines demonstrates well the complexity of these stress hormones.

When one is lacking or in excess, the others are also affected.
13/13
🔸Adrenal insufficiency is associated with decreased epinephrine
🔸PNMT synthesizes epinephrine and is regulated by glucocorticoids
🔸In adrenal insufficiency, PNMT activity decreases, leading to decreased epinephrine and one mechanism of hypotension

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More from @tony_breu

31 Oct
1/15
Why are statins administered at night?

In this tweetorial I'll discuss the mechanistic and historical reasons for the frequently used QHS dosing schedule. And why it's often unnecessary.

But before we get there, I'm curious: when do you prescribe/order/take statins?
2/
Early studies suggested that evening administration of statins led to a greater reduction in cholesterol when compared with morning dosing.

Two notes on the linked study:
➤It is small
➤The differences in LDL reduction weren't as clear

PDF: t.ly/6wfc Image
3/
As a result of this early data, the package insert for lovastatin, the first FDA-approved statin, suggested evening dosing.

And the landmark 4S trial did the same, administered simvastatin in the evening.

Insert: t.ly/GsOy
4S: t.ly/9mqS ImageImage
Read 15 tweets
14 Aug
As I noted in a recent tweetorial, Raymond Pearl reported a lower frequency of cancer in those with evidence of tuberculosis.

This finding led Pearl and others to treat patients with tuberculin.

Unfortunately, Pearl's original study methods suffered from bias.
More specifically, Pearl's study sample contained an overrepresentation of exposed controls (i.e., control subjects who had died from tuberculosis).

This led to an incorrect conclusion that tuberculosis is associated with decreased rates of cancer.
Pearl published a "retraction" in Science.

While arguing that "any serious student of the matter" would agree that TB and cancer are rarely found together in the same person, he admits that concluding a mechanistic connection "may have been erroneous".

pubmed.ncbi.nlm.nih.gov/17777405/
Read 5 tweets
14 Aug
1/16
Why do we use a vaccine (BCG) to treat an unrelated malignancy (bladder cancer)?

Can infections really prevent/treat cancer?

Let's find out.
2/
This story begins in 1813 when Arsène-Hippolyte Vautier reported that patients suffering from gas gangrene experienced a decrease in the size of their malignant tumors.

An explanation (or even the causative bacterium!) wasn't immediately apparent.

pubmed.ncbi.nlm.nih.gov/28202530/
Read 19 tweets
26 Jul
1/15
Why does clostridium difficile infection (CDI) cause marked leukocytosis?

Many of you have likely seen a new WBC >20k and wondered "could this patient have CDI?"

Are you right to wonder? If so, why?
2/
To start, is there a connection?

One of the earliest studies examined patients with WBC >30k. They reported the following rates of CDI:

🔹20% of all cases (excluding those with heme malignancy)
🔹34% of patients with an infectious etiology

pubmed.ncbi.nlm.nih.gov/12032893/
3/
In another study included 60 patients with unexplained leukocytosis (WBC >15k) and found:

⚡️58% had CDI⚡️

And: leukocytosis preceded recorded symptoms of colitis in half of the patients.

pubmed.ncbi.nlm.nih.gov/14599633/
Read 15 tweets
11 May
Great list Avi!

I'll add some relevant links for a few of these.
💻K/Mg repletion often unnecessary

Here is a tweetorial on potassium repletion/replacement.

💻Wilson disease evaluation in acute liver failure often not needed

@ebtapper and @ShaniHerzig wrote a great article in the @JHospMedicine Things We Do For No Reason Series on nondirected testing for inpatients with severe liver injury.

journalofhospitalmedicine.com/jhospmed/artic…
Read 6 tweets
17 Apr
1/6
Does doxycycline protect against clostridium difficile infection (CDI)?

If so, why?

These questions came up on rounds yesterday. Here are some potential answers.
2/
One study found an adjusted hazard ratio of 0.73 for CDI with the use of doxycycline.

A separate meta-analysis supported this finding with an odds ratio of 0.62 with all tetracyclines. The forest plot is attached.

pubmed.ncbi.nlm.nih.gov/22563022/
pubmed.ncbi.nlm.nih.gov/29401273/
3/
One potential explanation is that tetracyclines have in vitro activity against C. difficile.

This was demonstrated in a study reporting that 84% of C. difficile isolates had an MIC of ≤0.25 mg/L to tetracycline.

pubmed.ncbi.nlm.nih.gov/19732094/
Read 6 tweets

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