Hypercalcemia

The following information is simply informational. It's intent is not to replace the advice of a veterinarian nor to assist you in making a diagnosis of your pet. Please consult with your own veterinary physician for confirmation of any diagnosis. Your pets life may depend on it.

  Calcium is used as a messenger to activate enzymes and regulate all sorts of body functions. Calcium is such a crucial component of our biochemistry that virtually any complete blood panel, whether human or veterinary will include a measurement  of calcium. Our bodies go to tremendous lengths to regulate our blood calcium levels within a very narrow range. We need a storage source to draw upon for when we need more circulating calcium as well as a system to unload excess.

How Calcium is Organized in Our Bodies:

Calcium exists in several states in our bodies depending on whether it is being used or stored. “Ionized Calcium” is circulating free in the bloodstream and is “active” or ready to be used in one of the numerous body functions requiring calcium. The amount of ionized calcium in the blood is tightly regulated. Too much is dangerous. Too low is dangerous. About 50% of blood calcium is present as ionized calcium.

“Bound Calcium” is also circulating in the bloodstream but it is not floating around freely.  It is instead, being carried by molecules of albumin (a blood protein whose job is to transport substances that don't freely dissolve in blood) or complexed with other ions. About 40% of blood calcium is bound (i.e. carried by albumin or complexed with another ion).

Calcium is also stored in the minerals of bone. We do not usually think of bone as more than just scaffolding but living bone is a surprisingly active tissue. One of its functions is to store calcium and when calcium is needed,  it can be mobilized from the bone. Normally there is plenty of calcium and such mobilization does not significantly weaken the bone structure but if excess calcium is mobilized, bone can be depleted and softened.

 

Adjusting Calcium Levels

When the body needs to raise blood ionized calcium levels, the sources it may draw from are the bones (where calcium is stored as mineral), and the intestine (where the calcium we eat enters our bodies). We can regulate how much dietary calcium is allowed to enter from the GI tract. We can cause our bones to relinquish stored calcium quickly or slowly as our needs dictate.

When we want to drop the ionized calcium level, our kidneys are able to remove circulating calcium, including it in our urine so that it can be happily flushed away.

These processes are controlled by two hormones: “parathyroid hormone (affectionately called “PTH”) and “calcitriol (affectionately known as “vitamin D”). Calcitriol acts to enhance calcium absorption into the body from the intestine, promote release of calcium from bone, and cause the kidney to avoid dumping calcium. This adds up to higher blood ionized calcium. PTH also acts to mobilize bone calcium and shut off renal calcium dumping. This also adds up to more blood ionized calcium.

What keeps calcium from rising higher and higher?  Calcitriol shuts off PTH production in the parathyroid glands. PTH is necessary for activation of vitamin D. Essentially these two hormones shut eachother off.

The sequence of events might be this: blood ionized calcium begins to drop. The parathyroid glands sense this and release PTH. Ionized calcium begins to rise. When PTH levels are high enough,  vitamin D is activated. Ionized calcium begins to rise more. When enough vitamin D has been activated, the parathyroid glands shut of PTH production. When PTH levels are low enough, vitamin D activation ceases.

 

Why High Calcium Levels are Bad:

Elevated calcium starts with the bones. They receive an inappropriate message to mobilize their calcium. This message is either from excess parathyroid hormone or from high amounts of parathyroid hormone-related protein (see later). When calcium is removed from the bones, all that is left is a fibrous scaffold which is not really strong enough to support us. Our bones break, even fold.

Our kidneys normally would perceive these high calcium levels and attempt to unload as much calcium as possible into the urine. If parathyroid hormone levels are high, they are completely prevented from doing so. Without the ability to unload calcium, the kidney's system for water and sodium conservation is impaired. The result is excessive urine production (and often excessive thirst to match). In time, the excess calcium levels going through the kidney are damaging and kidney failure results. Calcium begins to deposit in all the body's soft tissues actually mineralizing them. This is a painful and inflammatory process.

So how can this system that seems so perfect get all screwed up and allow blood calcium level to rise so high? One common monkey wrench in the works is excess Parathyroid Hormone-Related Protein.

 

What Causes  Hypercalcemia?

Given the feedback system described, the list is rather short:

 (altering the calcium and phosphorus balance). It should be noted that kidney failure causes hypercalcemia and hypercalcemia causes kidney failure. It will be difficult to determine which came first but since kidney failure tends to progress rapidly in the presence of hypercalcemia, this puts more a rush on the testing sequence.

Back to the patient with an elevated calcium level that needs to be tracked down.  Often the elevated calcium is found as an unpleasant surprise on a screening test for a patient that, at least at first glance, seems  normal.

STEP ONE: Repeat the calcium level to be sure it is really elevated.
One might ask why does this particular test need to be repeated when in almost all other types of testing, the results are simply believed to be true and repeating is not necessary. The answer is that calcium is special. The materials used in testing calcium are not as stable as those for other tests.  Further, as you are about to find, the medical work up for hypercalcemia can be long and not inexpensive. For these reasons, we want to be absolutely certain about the hypercalcemia before launching the expedition that is the hunt for hypercalcemia.

STEP TWO: Double check the patient for obvious disease that might elevate calcium.
This is particularly important if the elevated total calcium was a surprise finding. The patient will be back in the hospital for a fresh blood sample as above; this is the perfect opportunity to feel the throat carefully for a possible parathyroid growth, do a rectal exam to rule out anal gland tumor, check all the lymph nodes for enlargement.  Mammary glands should be carefully checked for growths. Obviously if any of these are found, we have a direction to pursue and further testing may not be needed but if nothing is found

STEP THREE: Run a PTH level, an ionized calcium level, and a PTH-rP Level and an ACTH Stimulation Test to rule out Addison's Disease
Before launching a search for a hidden tumor (expensive and potentially invasive) it is probably worth exploring the non-invasive forms of testing first. The ACTH Stimulation test will require one or two hours in the hospital and is the only way to rule out the very treatable Addison's Disease (an adrenal hormone deficiency) as a cause of the elevated calcium. In one study of 40 dogs with elevated calcium, 29% had Addison's disease, making this condition a common cause of hypercalcemia (though not as common as Lymphoma and Parathyroid tumors).

The constellation of these tests will tell us if we must search for a parathyroid tumor, search for another type of tumor, treat for Addison's disease, or attempt to manage the kidney disease.

STEP FOUR: The Tumor Search

At this point, we have done all the blood testing we can do and ruled out Addison's disease, parathyroid tumor, and primary kidney disease. We are looking for a tumor that is not readily apparent and lymphoma is the most common. Again, we would like to reserve the most expensive and the most invasive testing for last in case they are not necessary. With this in mind, the following would be a reasonable sequence:

It should be obvious from this discussion that treatment of hypercalcemia is highly dependent on finding the underlying cause and treating that. One might ask is there nothing that can be done to control hypercalcemia during all this testing. The answer is “yes and no.” Treating the hypercalcemia is likely to interfere with the testing (see below).

Prednisone

It might seem like prednison e is useful in treating almost any disease. When it comes to hypercalcemia, prednisone enables the kidney to dump extra calcium and potentially bring dangerously elevated calcium levels down to normal. There is a very important downside here, however.  Lymphoma  remains the most common cause of hypercalcemia by far. Lymphoma cells are killed by prednisone and a short-term remission is induced. This sounds like it would be a good thing but in fact, it is not. If the hypercalcemic patient is put on prednisone before proper testing has been done, a lymphoma may be almost impossible to find thus making it almost impossible to reach a definitive diagnosis. Worse still, the remission achieved by prednisone alone is short-lived and leaves the tumor resistant to other chemotherapy drugs (thus making a long term remission all the more difficult to achieve).  For this reason, prednisone treatment is a last resort and is only used when testing has been exhausted.

Saline Diuresis

Hospitalization on intravenous fluids will help maintain blood flow to the damaged kidneys and may be useful. In general fluids not containing calcium are used. Low doses of frusomide also help remove calcium from the blood stream but one must be careful not to allow the patient to get dehydrated since furosemide is a diuretic (meaning it increases urine production).

As one can see a surprise elevated calcium test is not something to ignore.  Testing must be swiftly performed so that treatment can be initiated without fear of making diagnosis impossible.  If you have further questions about hypercalcemia or the conditions leading to it, do not hesitate to ask your vet

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