Instalab
logoInstalab

Valerate

Stool Test
See whether antibiotics or diet have thinned out the gut bacteria that, in early studies, help hold off C. difficile.
4.9 (4,676 reviews)
Tested by Diagnostic Solutions Lab
Physician-reviewed results
Results in under 1 week
How it works
Order from Instalab
No prescription or your own doctor's order needed
Self-collect at home
Kit shipped directly to you
Get results
Explained with clear next steps, no medical jargon

Should you take a Valerate test?

This test is most useful if any of these apply to you.

Healthy but Want to Stay Ahead
A baseline now lets you see how your gut bacteria's output shifts over the years as the science on this marker develops.
Recently Finished Antibiotics
Antibiotics can strip out the bacteria that make this fatty acid, and retesting can hint at whether your gut community is recovering.
Dealing With Recurring Diarrhea
Read with other stool markers, a low result can point toward a depleted bacterial community worth investigating further.
Changing How You Eat
Tracking this alongside other fermentation acids gives you an exploratory look at how a new diet is changing your gut bacteria's activity.

About Valerate

When a stool report lists a valerate number, it is showing one small trace of what the bacteria in your colon did with the last few days of food. Lab work and small human studies have tied this fatty acid to the gut's ability to keep C. difficile from taking over. C. difficile is the bacterium behind much of the severe diarrhea that can follow a course of antibiotics.

This is an early-stage research marker. There are no agreed cutpoints, and most of what's known comes from lab models, mice, and small studies. Its value for you lies in seeing your own pattern over time, read alongside the other fermentation products on the same report.

What Valerate Is

Valerate (valeric acid, also called pentanoic acid) is a short-chain fatty acid with five carbon atoms. Some researchers class the five- and six-carbon acids as medium-chain instead. Your own cells make very little of it. Most of it comes from bacteria in the colon fermenting leftovers you didn't absorb higher up, the same process that produces the better-known short-chain fatty acids acetate, propionate, and butyrate.

Valerate is a minor product of that fermentation, present in much smaller amounts than those three. Most of it comes from bacteria breaking down protein and amino acids, with some made by bacteria that feed on other fermentation products such as lactate and propionate. That's why many labs group it with the protein-fermentation acids rather than the fiber ones. The stool level reflects how busy a particular slice of your gut bacteria is, minus whatever your colon absorbed before the stool left your body.

The name causes a lot of confusion. Estradiol valerate (a hormone drug), betamethasone valerate (a steroid skin cream), valproate (a seizure and mood medicine), and dimethylguanidino valerate (a blood metabolite studied in diabetes and heart disease) are all different molecules. Research on any of them tells you nothing about this stool result.

C. difficile and the Gut's Own Defenses

The strongest reason to pay attention to stool valerate comes from work on C. difficile infection. In laboratory models of the human gut, valerate fell sharply when the antibiotic clindamycin wiped out much of the bacterial community, and adding valerate back slowed C. difficile's growth. The same research found valerate was low in stool from people with recurring C. difficile infection and rose after they received a stool transplant from a healthy donor, and a compound that releases valerate in the gut reduced C. difficile in mice.

Those findings suggest valerate is one of the chemical signs of a crowded, well-established bacterial community that leaves this pathogen little room to grow. The human data are small and come from people who were already sick with repeat infections, though, and a low stool valerate in someone without symptoms has not been shown to predict infection.

What this means for you: if you've had several rounds of antibiotics, keep getting diarrhea, or have had C. difficile before, a low valerate together with low levels of the other fermentation acids is a fair reason to look harder at your gut bacteria. A single low number on its own isn't a diagnosis of anything.

Bone Density

A human study combining gut bacteria sequencing with blood metabolite measurements linked a common gut species, Bacteroides vulgatus, to lower bone mineral density and linked valeric acid in the blood to higher bone density, with supporting experiments in mice. Blood valeric acid is a related but different measurement from stool valerate, and that work did not test whether a stool reading predicts your own bone density. The associations were modest and haven't been confirmed in independent groups, so treat it as an early lead.

Why One Reading Is Not Enough

Stool chemistry shifts with what you ate over the previous few days, how fast things are moving through your gut, and how the sample was handled. Because valerate is present in small amounts, it can swing noticeably from one collection to the next without any lasting change in your gut.

Collect each sample the same way, on a fairly typical diet, so a comparison between tests means something. With no standard cutpoints yet, your own trend is the most useful reference you have.

When Results Can Be Misleading

  • Stool consistency: results are reported per gram of stool, so very watery or very hard stool can push the number down or up without any real change in your bacteria.
  • Recent antibiotics: a course in the past several weeks reshapes the gut community for a while, so a reading taken then captures that disrupted state. Wait until your digestion is back to normal before taking a baseline.
  • Unusual eating in the days before: a sudden diet change, a few days of very different food, or a short fast shifts fermentation and can move a single reading.
  • Sample handling: short-chain fatty acids evaporate easily and bacteria keep fermenting after collection, so delays, warmth, or not following the kit's preservation steps can shift the result.

Labs measure stool short-chain fatty acids with different methods and report them in different ways, so compare results only from the same lab and the same test.

What Moves This Biomarker

Evidence-backed interventions that affect your Valerate level

↓ Decrease
Take the antibiotic clindamycin (studied in laboratory gut models for this marker)
In laboratory models of the human gut, clindamycin depleted valerate along with much of the bacterial community, and losing valerate left C. difficile free to grow. That fits with why antibiotic courses are a major setup for C. difficile infection, and why a low valerate soon after antibiotics likely reflects a real, if often temporary, disruption of your gut bacteria.
MedicationStrong Evidence
↑ Increase
Receive a fecal microbiota transplant
In people with recurring C. difficile infection, stool valerate was low before a stool transplant from a healthy donor and rose afterward. In laboratory gut models, valerate wiped out by antibiotics came back only after donor stool was added, and the restored valerate slowed C. difficile growth. A stool transplant is a medical treatment for recurrent C. difficile infection, so it is not something to pursue to change a number.
ProcedureModerate Evidence
↑ Increase
Take a multi-species probiotic or synbiotic (probiotic plus fiber) supplement daily
These supplements may nudge your valerate up. In a 12-week randomized trial in men with abnormal blood lipids, a multi-species synbiotic raised fecal valerate along with acetate, propionate, and butyrate, and also raised an anti-inflammatory signal in the blood. A second small trial of a multi-strain probiotic in postmenopausal women with obesity raised stool short-chain fatty acids as a group. That's a single small trial for valerate itself, so expect a modest and individual response.
SupplementModest Evidence

Frequently Asked Questions

References

13 studies
  1. Mcdonald J, Mullish B, Pechlivanis a, Liu Z, Brignardello J, Kao D, Et Al.Gastroenterology2018
  2. Lin X, Xiao H, Liu HM, Lv WQ, Greenbaum J, Gong R, Et Al.Nature Communications2023
  3. Ottosson F, Ericson U, Almgren P, Smith E, Brunkwall L, Hellstrand S, Et Al.Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease2019
  4. García-gavilán J, Atzeni a, Babio N, Liang L, Belzer C, Vioque J, Et Al.The American Journal of Clinical Nutrition2024