DUTCH Test Review: Is It Worth It? An Honest Doctor's Guide
I have no commercial interest in this test or its provider. See how I work and how treatment is structured.
Dr Shehan Wijesingha MD, M.TCM, BMedSci, DipAP, CPT
Over the last few days, whilst I was finishing this article, I started talking with a young woman who had just moved into my home. After some discussion, she described a difficult period in her life, with various symptoms across her body. She went through the conventional medical system, and the doctors could not find anything wrong with her.
She described how this all changed when she saw a functional medicine doctor, who ordered a DUTCH test.
Following this, she was prescribed a protocol, hormonal treatment, supplements and nutritional guidance, tailored to her. She described how she finally understood the root cause of her problems and that truly made a difference. It also allowed her to be taken more seriously by her conventional doctors.
Despite spending between $4,000 and $5,000 in the U.S. on the testing, the supplements and the repeat specialist appointments, she seemed genuinely happy with what this test had given her. And I can understand why. For a person genuinely suffering with significant health issues, nothing at that point matters more than getting better.
At the same time, she did admit something afterwards. Things truly got better once she removed the source of stress from her life.
This is unlikely to be an isolated case. But it does leave the primary question, from my perspective: could these results have been achieved without this test? Was this test fundamental to her recovery, or is there a more cost-effective solution that could have provided similar, or even better, results at the time?
That is the purpose of this article.
Summary
- What it is: The DUTCH test is a dried urine test ordered by functional and integrative practitioners. Its flagship version measures roughly 35 hormone-related markers.
- What it claims: Its central claim is that it measures sex hormones, cortisol, melatonin, their metabolites and some precursors across a day or a menstrual cycle. Therefore it claims to additionally show how your body is processing and clearing them, something a single blood test cannot show.
- The chemistry: I believe the underlying chemistry is valid. Dried urine steroid profiling by LC-MS/MS is established in some contexts, and measuring hormones across a day or cycle is biologically plausible.
- The evidence: The interpretation and clinical utility are thinner. Most studies come from its founder and company, there are no large randomised controlled trials, and some gynaecological societies advise against urine or saliva hormone tests to guide hormone dosing.
- What it is not: It is not a diagnostic tool. It does not diagnose Cushing’s, Addison’s, PCOS or “adrenal fatigue.” It costs $499 out of pocket and does not appear in conventional guidelines.
- My position: I do not use it routinely, I have no commercial interest in it, but I do not think it is a scam. I would consider it around hormone therapy decisions, for multi-system symptoms after normal bloods, or in chronic stress, sleep and fatigue, if cost is not an issue and the patient wants a wider picture alongside conventional care.
- What would change my mind: I am open to changing my mind if reliable third-party data emerges showing that treatment guided by DUTCH testing improves outcomes.
What is the DUTCH test?
The DUTCH test is a home test typically ordered by functional and integrative practitioners to test your sex hormones, your stress hormones, your sleep hormones and their metabolites in one test. It is often read alongside your wider clinical picture, your lifestyle and your wellbeing goals, to add context to your symptoms.
The rationale for this test is that hormones such as cortisol and testosterone rise and fall across the day, and female hormones change across your menstrual cycle.1, 2 Therefore this method, compared to a blood test taken on a single day, can help better reflect that and create a better understanding of the pattern of symptoms you may be experiencing.
However, at $499, this test is definitely not cheap, especially in some countries.3 You can go to the public system and get a lot of tests done for free under a gynaecologist, urologist, endocrinologist, or local GP.
It is a test that conventional doctors rarely order, because it is not recommended in current medical guidelines.4–6
Therefore, the most important question for a person who truly wants to get better may be: is the DUTCH test a test that can genuinely help make a long-term difference to their health, is it just an expensive scam to exploit vulnerable patients, or is it somewhere in the middle?
This article is my honest answer to that question.
My genuine interest is that I hope the reader, amongst various other sources of information, can make a more informed decision, take charge of their health, and return to themselves.
What does the DUTCH test measure?
Depending on the panel, the DUTCH test is said to measure roughly 35 markers that fall into a number of categories:7
- your sex hormones
- your stress hormone, cortisol
- your sleep hormone, melatonin
- their metabolites: the breakdown products of these hormones once they have done their job
- some of their precursors: the chemicals they are built from
This whole picture is therefore claimed to provide additional information on your hormone levels, on how the hormones are working in your body, and how they are being processed and cleared.
The hormones
- Oestrogen: the three main types are oestrone (E1), oestradiol (E2) and oestriol (E3). Oestradiol is the most biologically active and is involved in reproductive health, mood regulation and bone density.8–10
- Progesterone: measured through its metabolites (the pregnanediols),11, 12 helps to regulate the menstrual cycle and maintains pregnancy.13–15
- Testosterone and other androgens: including DHT, a more potent testosterone metabolite. It is often thought of as a male hormone, but women need it too, for muscle mass, energy and libido.
- DHEA-S: both a hormone and a precursor. The adrenal glands produce it, and the body converts it into oestrogen and testosterone.
- Cortisol and cortisone: free cortisol (the active form) is measured at four to five points across the day, alongside cortisone, the less active form, and metabolised cortisol, which reflects total output.1, 16
- Creatinine: a byproduct of muscle breakdown, not a hormone.
- Melatonin: measured through one of its metabolites (6-OH-melatonin-sulfate), relevant to how you fall asleep, stay asleep, and wake.17
The metabolites
This is where the DUTCH test differs from most standard testing, because blood tests tell you how much of a hormone is circulating at one moment. The DUTCH test is said to also show how your body is processing and clearing it.
Functional medicine and integrative doctors would typically argue that this is where the explanation for symptoms lives. A clear example they may use is oestrogen. They would argue that it does not leave the body one way: it is funnelled down three competing pathways (2-hydroxyestrone, 4-hydroxyestrone and 16-hydroxyestrone), and the report measures the metabolites from each.12, 18 They would argue that which pathway dominates, and how well your body caps off the intermediates, is information a standard blood test cannot give you.
I will come back to much of this rationale in the sections about sex hormones, HRT and fertility and cortisol.
The organic acids
Depending on the panel, the DUTCH test also includes a small set of organic acid markers, byproducts of metabolism that are claimed to hint at nutrient and metabolic patterns.7, 19 I have written more information on the organic acid test, which measures many more of these markers on its own.
How is the DUTCH test done?
The DUTCH test is done by peeing onto small filter paper strips, or collecting your urine in a clean cup and dipping the strip. This is done at set times across the day. The strips are then allowed to dry fully, sealed into a labelled pouch, and posted back in a prepaid envelope to the laboratory.7, 20 You do not need to visit a clinic, so this can all be done at home. Your kit will have detailed instructions, which are the definitive guide.20 Everything below is a typical pattern, so you can understand what you are signing up for.
Before you collect
This applies to the DUTCH Complete and DUTCH Plus. Cycle Mapping is a different story, and the kit instructions are the guide.
If you are a menstruating female with regular cycles, the aim is to collect in the mid-luteal phase, roughly a week after ovulation, when progesterone is at its peak.13 In a 28-day cycle, that is around days 19 to 22.20, 21 In a 30-day cycle, around days 21 to 24.21 In a 26-day cycle, around days 17 to 20.21 If you are postmenopausal or a man, any day will do.20, 21 If your cycles are irregular or you are perimenopausal, follow the kit’s timing guidance.20
Things to consider stopping before the test
- Melatonin supplements: if a baseline is wanted, stop 2 to 3 days before, because the test measures melatonin metabolites, so supplements can interfere with interpretation.17
- Prescription medicines: discuss with your practitioner before stopping anything.
- Alcohol for 24 hours before and on collection days, and caffeine beyond one cup (about 240 ml), as this can affect hydration, and any markers that may be affected as a result.20, 22
- Total fluids: drink no more than about 1.2 litres on collection days, and nothing in the 2 hours before a collection, to prevent very dilute urine that can shift the result.20, 22
- Foods such as bananas and fava beans for 48 hours before, as they are rich in amines, which your body converts into neurotransmitter metabolites.22 The current kit also lists creatine supplements.20, 22
- An unusually stressful day: not easy to avoid, but it can affect cortisol levels. It may not be an adequate reflection of your baseline.
The collection day
Four or five samples, at roughly these points across 24 hours:7, 20
- Dinnertime
- Bedtime
- Overnight, only if you wake to urinate
- Within 10 minutes of waking
- 2 hours after waking
After this has been sent to the laboratory, you will receive a thick, colour-coded report of dozens of markers. This is where you can work with a practitioner who understands your context and wider picture, and discuss together whether there is anything worth acting on. If so, why? If so, how?
Which DUTCH test should you choose?
There are three main versions:
- DUTCH Complete: the flagship, containing roughly 35 markers across the three panels above.7, 23
- DUTCH Plus: the DUTCH Complete plus a cortisol awakening response. This means a series of saliva samples, on waking and 30 and 60 minutes after waking, to take further measurements of cortisol.22, 24, 25 It may typically be considered in fatigue (especially on waking), insomnia, chronic fatigue, depression or anxiety on waking, and a high-stress lifestyle.24
- DUTCH Cycle Mapping: samples taken across the menstrual cycle to map how hormones rise and fall throughout the whole cycle.26 Typically considered for perimenopause, PCOS and infertility.
The three versions at a glance
| Version | What it measures | How you collect | US price3 |
|---|---|---|---|
| DUTCH Complete7 | Sex hormones, cortisol, melatonin and selected organic acids | Four or five dried urine samples over 24 hours | $499 |
| DUTCH Plus24 | Everything in the Complete, plus the cortisol awakening response | The same urine samples, plus saliva on waking and 30 and 60 minutes after | $650 |
| DUTCH Cycle Mapping26 | Oestrogen and progesterone across the whole cycle | First-morning urine samples across one menstrual cycle | $550 |
What does the DUTCH test claim to show?
The DUTCH test claims to show the following, depending on the panel:7, 24, 26
-
Diurnal cortisol rhythm across the day
-
Cortisol awakening response, if Plus
-
Sex hormone patterns across the cycle, if Cycle Mapping
-
Oestrogen metabolite ratios: 2-OH, 4-OH, 16-OH
-
Cortisol-to-cortisone and androgen 5α-to-5β ratios
-
Melatonin metabolite and selected organic acids
Whilst this test may potentially seem like an obvious choice, the biggest question may still remain: how likely is it to explain what is going on with you? How likely is it to help improve treatment? What is that treatment likely to be? And is that treatment something that aligns with your values and budget? Hopefully, the rest of this article can help answer those questions.
What can the DUTCH test genuinely add?
The benefits of this test are that you do not have to go into a clinic: you can do it at home. It can measure hormones across a full day or your full menstrual cycle, as opposed to a snapshot in time via blood tests. And it can help create a wider picture of the levels of your sex hormones, adrenal hormones and organic acids, as well as how your body is processing and clearing them. These can all be read together, in the context of your wider clinical picture.
Convenience and access: Having worked myself in both the public and private conventional medical setting, I have seen how patients who were seen faster in the private setting, could be treated before the consequences of their condition got worse. Therefore, being able to do this test at home and see all of these results in one go can potentially provide additional value to any other tests you may have been ordered separately by your GP, your endocrinologist, your gynaecologist or your andrologist. You can see these results at the same time, ideally assisted by a practitioner who understands how all of these interact, as opposed to seeing each of them separately, at different times.
A rhythm, not a snapshot: Measuring four or five samples of urine over 24 hours, or multiple samples across your entire menstrual cycle, does make sense. We do a 24-hour ECG and urine collection in conventional medicine for example when indicated, to get a more comprehensive picture of what is happening in the body. This test applies the same logic to hormones.11, 19
Metabolites as a hypothesis, not a diagnosis: Functional medicine and integrative practitioners will typically use terms such as adrenal dysfunction, oestrogen dominance and impaired hormone metabolism, based on metabolite patterns, to identify what they describe as the root cause. I think a better way of thinking about it is that this tool can be used to generate a hypothesis, based on how your body is processing and clearing hormones. For example, pathways such as the relatively protective 2-OH pathway vs the more proliferative 16-OH route, as well as ratios such as cortisol to cortisone, androgen 5α to 5β, and oestrogen metabolites can be read in the context of how each person metabolises hormones uniquely.18, 27
Hormones in context: Reading results such as your cortisol, your DHEA and your sex hormones: these all affect each other. Whilst they can provide an explanation for a person struggling with fatigue or burnout, mood swings and low energy, it is best understood as helping to understand the wider picture, as opposed to a diagnosis. The wider picture, in the context of other factors: your environment, nervous system, Ayurvedic and Chinese medicine diagnosis as well as your mind-body-spirit-energy system (from my perspective).
Monitoring treatment, with cost caveats: Just like in conventional care, you could use the test as a baseline and then retest at a certain point later, combined with your clinical presentation and how you feel,28 to get objective feedback on whether certain interventions are working, and to help tailor conversations about further management if needed.29 What needs to be taken into consideration here is the further cost that comes with further testing, treatment and practitioner appointments. This is a decision that should be made by yourself first and foremost, and with any practitioner you choose to work with.
What are the limitations and evidence gaps?
- The chemistry vs the interpretation. Whilst measuring metabolites in dried urine using LC-MS/MS is well established,30, 31 and the cortisol daily rhythm and basic sex hormone metabolites seem well supported,1, 11, 19, 32 the interpretive framework, and what should follow from it, is where the evidence becomes variable. Using it to guide HRT dosing, or to make decisions from a particular oestrogen metabolite ratio, we simply do not yet have evidence that decisions based on these urine measurements improve outcomes.5, 6, 33
- Founder-led studies and lack of RCTs: All published validation studies on the DUTCH test have been led by its founder, Mark Newman, and his company.1, 11, 19, 29 It has not been cleared by the FDA,5, 34, 35 and there are no large randomised controlled trials validating its use in the way medicine normally demands. Some gynaecological societies advise against urine or saliva hormone tests to guide hormone dosing, and it does not appear in clinical practice guidelines, most likely for many of these reasons.4–6 It simply does not have the decades of long-term research behind it that many traditional tests have.
- Guidelines and regulatory status: It should not be used as a substitute for conventional care. Not to diagnose medical conditions such as Cushing’s syndrome, Addison’s disease or PCOS, which require conventional investigation, such as the ACTH stimulation test for Addison’s disease.36–38 Not to predict breast cancer risk, which uses conventional pathways such as family history and genetic testing, with breast screening where indicated.39 Not to guide HRT decisions, which are based on symptoms, age, menopausal status, risk profile and clinical judgement.4, 6 And it cannot diagnose adrenal fatigue, which is not a recognised medical diagnosis.40, 41 It is intended to provide a wider clinical picture, and patients should genuinely understand its purpose before spending anything.
- Cost, variables and reliability: It is expensive, and typically will not be covered by insurance or any government pathway.23 The at-home collection needs to be done properly, as day-to-day variables such as diet, hydration, medications, supplements and collection technique can change the result.20
- Timeframe: a day or cycle vs weeks, months and years: Compared to a single blood draw, four or five samples across the day, to me, seems like a genuine improvement. But most people’s question is not what has been happening to me yesterday or today. The question is what has been going on in my body over the last few weeks, months and years. If a stressful day can change the cortisol pattern, or if a number of foods can change the organic acid markers, how accurate and reliable is this test to truly add additional information?
- Overinterpretation: treating numbers instead of the person: Imagine someone with years of stored trauma, poor sleep and exhaustion. They spend thousands on tests and supplements when the simpler, deeper solution was nervous system and stress work. The test should add context to the person’s story, not replace it.
- The Practitioner Factor: They need a genuine understanding of the biochemistry in depth, of the methods and limitations of this test, and of the extent to which the results are most likely contributing to this patient. Whether it is important to add something, change something, or do nothing. That comes from the practitioner and their genuine determination and curiosity to understand all sides of this argument.
What the DUTCH studies tested
| Study | What it compared | Who ran it | What it found | Still untested |
|---|---|---|---|---|
| Dried urine and blood11 | Dried urine sex hormones against blood, and four dried samples against a 24-hour collection | The company, with outside co-authors | Close agreement | Whether patients do better |
| Dried urine and saliva1 | The daily cortisol pattern in dried urine against saliva | The company | Close agreement | Whether patients do better |
| Reliability19 | Dried against liquid urine, and four samples against a 24-hour collection | The company | Close agreement for most hormones | Whether patients do better |
| HRT patches29 | Dried urine oestrogen in women using patches | The company, with a university co-author | Urine tracked the dose | Whether urine-guided dosing is safer or works better |
Why the evidence gap exists
I think innovation is definitely needed to drive the medical profession forward. Pharmaceutical companies have very large budgets to fund the randomised controlled trials needed to determine the efficacy of medications, but is the same level of funding used to trial supplements, protocols and clinical judgement? Whilst it is understandable that evidence is needed, it is also worth understanding the value of interpretation and rationale from the practitioner, and whether a randomised controlled trial is even the best research method to determine the efficacy of a treatment, considering the level of personalisation that would truly be required to enable healing.
Blood vs saliva vs dried urine: which is best?
There is no single best test. Each test can be the best one to order in certain situations, depending on the question you want answered:
- Blood tells you what is circulating at that moment.
- Saliva tells you what is unbound and available at that moment, for some hormones, such as cortisol.37, 42
- Dried urine tells you what your body did with its hormones across the day.11, 19
These are different answers to different questions, and they can be used together.43 It does make sense that they could provide a more complete picture of what may be going on.
Blood is often the right tool for acute problems, and to diagnose specific conditions such as premature menopause or testosterone deficiency.2, 4 It is what most guidelines are built on. It is standardised, inexpensive, and can often be done free through government healthcare systems.
Saliva can be done at home. It measures the free form of some hormones, and is used in certain medical guidelines, for example to screen for Cushing’s syndrome,37 and has been studied in relation to coronary calcification.44 Food and oral hygiene may affect the sample,22 and it may not capture every hormone reliably.42 Some practitioners who use it to dose topical testosterone may end up underdosing patients.45
Dried urine is the one that shows you both the hormones and what your body is doing with them.
The right test depends on the patient’s situation. Factors such as significant kidney impairment, pregnancy, being on HRT or the contraceptive pill, or certain medications should all be taken into account, as well as cost, when deciding whether the patient needs one of these methods or multiple, to get a wider picture.12, 46
Cortisol and stress: where DUTCH may add context
With stress, burnout and lifestyle overwhelm now so common, I do think cortisol dysfunction is heavily underrecognised in conventional medicine. It can mimic and magnify symptoms such as fatigue, sleep disruption, anxiety and weight gain whilst going undetected in the conventional setting. Heart disease, one of the world’s biggest killers, can be associated with a flattened stress rhythm.44, 47, 48 The HPA axis, from my perspective, can be completely dysregulated as a result of stress. Conventional medicine can test the reserve of the HPA axis, through an insulin tolerance test, though that is impractical for routine use.49
The most important question here is: what would be the solution? I think the biggest value of this test is reassurance to a patient that it is not all in their head, which, I do not underestimate at all, can be hugely relieving, especially after years of being palmed off.
However, I would take it one step further. I would argue that a lot of the patients that come to me already know they are stressed. I just listen to them and I can see what has caused certain issues. I can feel their pulse from a traditional Ayurvedic and Chinese medicine perspective to see what meridians are blocked. I listen to their story, which may stem from early life, to see where stress may have accumulated in their body, understanding this from an Ayurvedic and Chinese medicine diagnostic framework combined with modern science.
The truth is, I do not need a test to believe what a patient is saying to me. The solution from a functional medicine doctor, from my perspective, might be:
- cut down on coffee
- reduce stress
- spend time in nature
- take some herbs and supplements
I am not against any of this. If anything, I use it. I advise a lot of it myself. But I do not need this test result to advise them.
To me, the solution is far deeper, as explained in my method. I think sometimes the genuine solution comes down to restoring your ability to truly react to stress, so you can react in a way you once may have been able to, and removing the stressor where practical. I have often got involved with speaking to the sources of the stressors myself, and I have seen powerful clinical results in the patient in front of me when I have done so. I do not need any of these test results to resolve the root cause in these instances. I think these are far more powerful methods of resolving underlying stress than any supplement, or cutting down on coffee, can provide.
However, I do understand the powerful benefit a patient can receive from seeing objective markers before and after a treatment intervention. I am probably shooting myself in the foot here when I say this, because testing this, from my perspective, would strengthen the validation of my own method. I would rather not spend the patient’s money to prove something to myself, and to others.
Sex hormones, HRT and fertility: what I would personally want to know
As a doctor trained in conventional medicine, I myself have not taken a single medication or undergone any surgery for over 20 years, for as long as the choice has been my own. Therefore I think what follows should be taken into account with this in mind.
Whilst I am aware of various conventional medical guidelines and recommendations, if it were my own body, I would be very cautious before taking treatment such as the oral contraceptive pill, testosterone replacement therapy, hormone replacement therapy, or IVF. I would personally be very cautious about starting female hormone replacement due to concerns such as breast cancer,50–52 stroke,51–53 blood clots51, 53, 54 and dementia,51, 55, 56 even knowing these risks vary with the type of hormone and how it is taken,6, 51, 54, 57 testosterone replacement due to concerns such as cardiovascular complications,58, 59 including atrial fibrillation and pulmonary embolism,60 even though the largest trial found no rise in heart attacks or strokes,60, 61 and IVF due to long term concerns both secondary to excessive ovarian stimulation and to my own child.62–65
Therefore, if it were my own body, I would want to make an as informed choice as possible.
Irrespective of what guidelines say, if it were my own body, and I were to take any of the above, I would personally want as much information as possible, specifically because of my concerns about the risks of taking all of this. I know the evidence for using these results this way is still at the research stage, so this is my personal preference, and I would weigh it alongside the conventional evidence.5 I would want to measure things like:
- the diurnal pattern of free cortisol, to see how my stress axis is behaving, knowing it has been linked to heart health44, 47
- DHEA, to see how my stress hormones and androgens are balanced
- my melatonin, knowing that stress and cortisol can suppress it17
- signs of oestrogen dominance which could explain some symptoms
- my oestrogen metabolite pattern, if I were about to start oestrogen, as one more piece of information while the evidence develops18, 27, 33
I would do the above in addition to following any recommended conventional care tests and measures. I would do my best to understand why functional or integrative medical practitioners may sometimes take a differing and/or complementary stance to conventional specialists and medical societies. I would also become more informed of the alternative solutions they may provide to conventional care such as gut healing programmes, detoxification protocols, progesterone creams, supplements, repeat testing and further appointments. And I may compare this to more ancient forms of healing such as Ayurveda and Traditional Chinese Medicine to see their more natural solutions to the same issues. I would then make a decision on which approach, or combination of approaches, I would wish to apply to my own body.
After understanding all of this, I would try to meet with a specialist who is genuinely, truly informed on all of this, who can match, at the very least, the research I have done by myself and ideally help me make a more informed decision on top of that. I may end up seeing multiple specialists, which may include an andrologist, a gynaecologist, a functional medicine doctor or an integrative medicine doctor, or ideally one who I truly trust, depending on the competence of such a practitioner in my country and their availability.
I would scrutinise their approach. Are they geared towards following conventional guidelines? Are they likely to prescribe a protocol of never-ending supplements, diets and compounded hormones, with repeated testing under the guise of monitoring? What is their commercial incentive? What would most likely be the options they recommend to help me? I would be cautious about their incentive to help me, and I would tend to follow my own intuition during this process.
Is the DUTCH test worth it? My verdict
Whilst most medical bodies and medical specialists may not advise this test, especially for diagnosis and to guide medical treatment, based on the information above I do believe the chemistry underlying this test is valid.
And currently if a patient would prefer to take replacement hormones or IVF, I would refer down the relevant pathways. However, patients rarely see me for this.
For these reasons, I do not use it routinely, nor do I currently advise it as a first-line test. But I would consider it in specific contexts. What would change my mind?
- If I were to ever start prescribing replacement hormones for patients to help obtain a wider picture of what may be happening at a biochemical level and guide better as part of a holistic treatment plan.
- If the patient made an informed decision that the likely benefits of having this test outweigh the cost for a more comprehensive understanding of their hormonal levels in addition to conventional pathways.
- If more reliable data were to be released, ideally from third parties, in relation to the efficacy of treatment based on DUTCH testing and its components.
After this, however, from my perspective, the gold standard of scientific inquiry going forward may have to include rigorous n = 1 trials alongside larger trials, to help move personalised medicine forward.66
Who I would consider it for, and who I wouldn’t
My primary goal is to create the best results for patients.
That being said, if I were going through any of the following myself, I would consider this test if:
- I were perimenopausal, menopausal or postmenopausal, to explore hormone patterns alongside menopausal care.
- I had multi-system symptoms which standard labs did not explain.
- I had chronic stress, sleep issues and fatigue.
- I had done blood work and still wanted answers.
- I had cyclical or mid-cycle symptoms.
- I was about to start the pill, HRT or testosterone and wanted a fuller picture before deciding.
I would not consider the DUTCH test if:
- I purely wanted a medical diagnosis.
- I was undergoing an acute medical crisis.
- I had significant kidney impairment.46
- I was pregnant or breastfeeding.
- I was a child or adolescent.
- I thought I might have a hormone-producing tumour.
- I was looking for a diagnosis of adrenal fatigue.40, 41
- I knew I had a significant likelihood of severe health anxiety as a result of what this test might show, which could make underlying health anxiety significantly worse.
- I wanted to start HRT, testosterone, DHEA or the contraceptive pill based purely on one test.
- I wanted to stop conventional medical treatment based purely on one test.
- I wanted to launch an extensive supplement regimen based purely on one test.
- I wanted to blindly follow the advice of a conventional, functional or integrative medicine specialist, without doing my diligent research first.
- I was on a tight budget, where the same money may be better spent on treatment and intervention.
What I would do if I were in your position
| Question | If yes | If no |
|---|---|---|
| Am I looking for a diagnosis? | Do not use DUTCH alone. See a GP/specialist. | Continue. |
| Have I done conventional bloods first? | Consider DUTCH as an adjunct. | Do them first. |
| Do I have red flags? Pregnancy, kidney impairment, acute crisis, possible hormone-producing tumour? | Do not do DUTCH. | Continue. |
| Can I afford test + consultation + follow-up + supplements? | Continue. | Spend the money on treatment instead. |
| Do I have a practitioner who will not overinterpret? | Continue. | Find one first. |
| Do I know what I would do differently with the result? | Consider it. | Do not test. |
| Could I reach the same decision without it? | Take the simpler route. | Consider it. |
If you are considering working with me, feel free to
References
- Newman M, Curran DA, Mayfield BP (2020). Dried urine and salivary profiling for complete assessment of cortisol and cortisol metabolites J Clin Transl Endocrinol 22:100243.
- Bhasin S, Brito JP, Cunningham GR, et al (2018). Testosterone therapy in men with hypogonadism: an Endocrine Society Clinical Practice Guideline J Clin Endocrinol Metab 103(5):1715-1744.
- Precision Analytical Inc (company document) (2026). DUTCH shop price list (read 5 October 2026)
- National Institute for Health and Care Excellence (2015). Menopause: identification and management. NICE guideline NG23 (published 12 November 2015, last updated 15 April 2026) NICE, London.
- American College of Obstetricians and Gynecologists (2023). Compounded bioidentical menopausal hormone therapy: ACOG Clinical Consensus No. 6 Obstet Gynecol 142(5):1266-1273.
- The North American Menopause Society (2022). The 2022 hormone therapy position statement of The North American Menopause Society Menopause 29(7):767-794.
- Precision Analytical Inc (company document) (2026). DUTCH Complete (product page, read 5 October 2026)
- Gruber CJ, Tschugguel W, Schneeberger C, Huber JC (2002). Production and actions of estrogens N Engl J Med 346(5):340-352.
- Khosla S, Oursler MJ, Monroe DG (2012). Estrogen and the skeleton Trends Endocrinol Metab 23(11):576-581.
- Schmidt PJ, Ben Dor R, Martinez PE, et al (2015). Effects of estradiol withdrawal on mood in women with past perimenopausal depression: a randomized clinical trial JAMA Psychiatry 72(7):714-726.
- Newman M, Pratt SM, Curran DA, Stanczyk FZ (2019). Evaluating urinary estrogen and progesterone metabolites using dried filter paper samples and gas chromatography with tandem mass spectrometry (GC-MS/MS) BMC Chem 13:20.
- Newman M (Precision Analytical Inc, company document) . Estrogen tutorial
- Reed BG, Carr BR (2018). The normal menstrual cycle and the control of ovulation (Endotext, updated 5 August 2018) Endotext, MDText.com.
- Mesen TB, Young SL (2015). Progesterone and the luteal phase: a requisite to reproduction Obstet Gynecol Clin North Am 42(1):135-151.
- Csapo AI, Pulkkinen MO, Wiest WG (1973). Effects of luteectomy and progesterone replacement therapy in early pregnant patients Am J Obstet Gynecol 115(6):759-765.
- Newman M (Precision Analytical Inc, company document) . DUTCH Complete cortisol tutorial
- Newman M (Precision Analytical Inc, company document) (2015). Melatonin testing update
- Fuhrman BJ, Schairer C, Gail MH, et al (2012). Estrogen metabolism and risk of breast cancer in postmenopausal women J Natl Cancer Inst 104(4):326-339.
- Newman M, Curran DA (2021). Reliability of a dried urine test for comprehensive assessment of urine hormones and metabolites BMC Chem 15(1):18.
- Precision Analytical Inc (company document) (2025). DUTCH Complete collection instructions (2025 version, current on the DUTCH site)
- Precision Analytical Inc (company document) (2021). DUTCH Complete collection instructions, one-page version (Ref042621)
- Precision Analytical Inc (company document) (2026). DUTCH Plus collection instructions (2026 version)
- Precision Analytical Inc (company document) (2026). Frequently asked questions about the DUTCH Test
- Precision Analytical Inc (company document) (2026). DUTCH Plus (product page, read 5 October 2026)
- Stalder T, Kirschbaum C, Kudielka BM, et al (2016). Assessment of the cortisol awakening response: expert consensus guidelines Psychoneuroendocrinology 63:414-432.
- Precision Analytical Inc (company document) (2026). DUTCH Cycle Mapping (product page, read 5 October 2026)
- Sampson JN, Falk RT, Schairer C, et al (2017). Association of estrogen metabolism with breast cancer risk in different cohorts of postmenopausal women Cancer Res 77(4):918-925.
- Ryan R, Booth S, Spathis A, Mollart S, Clow A (2016). Use of salivary diurnal cortisol as an outcome measure in randomised controlled trials: a systematic review Ann Behav Med 50(2):210-236.
- Newman MS, Mayfield BP, Saltiel D, Stanczyk FZ (2023). Assessing estrogen exposure from transdermal estradiol patch therapy using a dried urine collection and a GC-MS/MS assay Steroids 189:109149.
- Protti M, Mandrioli R, Mercolini L (2020). Microsampling and LC-MS/MS for antidoping testing of glucocorticoids in urine Bioanalysis 12(11):769-782.
- Protti M, Marasca C, Cirrincione M, et al (2020). Dried urine microsampling coupled to liquid chromatography-tandem mass spectrometry (LC-MS/MS) for the analysis of unconjugated anabolic androgenic steroids Molecules 25(14):3210.
- Handelsman DJ, Nimmagadda R, Desai R, et al (2021). Direct measurement of pregnanediol 3-glucuronide (PDG) in dried urine spots by liquid chromatography-mass spectrometry to detect ovulation J Steroid Biochem Mol Biol 211:105900.
- Obi N, Vrieling A, Heinz J, Chang-Claude J (2011). Estrogen metabolite ratio: is the 2-hydroxyestrone to 16α-hydroxyestrone ratio predictive for breast cancer? Int J Womens Health 3:37-51.
- US Food and Drug Administration (2025). Laboratory developed tests (regulatory status after the 2024 rule was vacated)
- Precision Analytical Inc (company document) (2026). Licensing and certifications (CLIA certification and proficiency testing)
- Bornstein SR, Allolio B, Arlt W, et al (2016). Diagnosis and treatment of primary adrenal insufficiency: an Endocrine Society Clinical Practice Guideline J Clin Endocrinol Metab 101(2):364-389.
- Nieman LK, Biller BMK, Findling JW, et al (2008). The diagnosis of Cushing's syndrome: an Endocrine Society Clinical Practice Guideline J Clin Endocrinol Metab 93(5):1526-1540.
- Teede HJ, Tay CT, Laven JJE, et al (2023). Recommendations from the 2023 International Evidence-based Guideline for the Assessment and Management of Polycystic Ovary Syndrome Hum Reprod 38(9):1655-1679.
- National Institute for Health and Care Excellence (2023). Familial breast cancer: classification, care and managing breast cancer and related risks in people with a family history of breast cancer. Clinical guideline CG164 NICE, London.
- Cadegiani FA, Kater CE (2016). Adrenal fatigue does not exist: a systematic review BMC Endocr Disord 16(1):48.
- McDermott MT (2025). Pseudo-endocrine disorders: recognition, management, and action J Endocr Soc 9(1):bvae226.
- Fiers T, Delanghe J, T'Sjoen G, et al (2014). A critical evaluation of salivary testosterone as a method for the assessment of serum testosterone Steroids 86:5-9.
- Coburn SB, Stanczyk FZ, Falk RT, et al (2019). Comparability of serum, plasma, and urinary estrogen and estrogen metabolite measurements by sex and menopausal status Cancer Causes Control 30(1):75-86.
- Matthews K, Schwartz J, Cohen S, Seeman T (2006). Diurnal cortisol decline is related to coronary calcification: CARDIA study Psychosom Med 68(5):657-661.
- Newman MS, Smeaton J, Gillson G, Jaferi A (2026). Alternatives to serum testing for transdermal testosterone monitoring: a review of clinical data and correlation with clinical response (Hypothesis and Theory article; three of four authors from Precision Analytical, the DUTCH laboratory) Front Reprod Health 8:1804311.
- Precision Analytical Inc (company document) (2023). Clinical validity of the DUTCH Test (booklet)
- Kumari M, Shipley M, Stafford M, Kivimaki M (2011). Association of diurnal patterns in salivary cortisol with all-cause and cardiovascular mortality: findings from the Whitehall II study J Clin Endocrinol Metab 96(5):1478-1485.
- Adam EK, Quinn ME, Tavernier R, et al (2017). Diurnal cortisol slopes and mental and physical health outcomes: a systematic review and meta-analysis Psychoneuroendocrinology 83:25-41.
- Fleseriu M, Hashim IA, Karavitaki N, et al (2016). Hormonal replacement in hypopituitarism in adults: an Endocrine Society clinical practice guideline J Clin Endocrinol Metab 101(11):3888-3921.
- Collaborative Group on Hormonal Factors in Breast Cancer (2019). Type and timing of menopausal hormone therapy and breast cancer risk: individual participant meta-analysis of the worldwide epidemiological evidence Lancet 394(10204):1159-1168.
- Marjoribanks J, Farquhar C, Roberts H, Lethaby A, Lee J (2017). Long-term hormone therapy for perimenopausal and postmenopausal women Cochrane Database Syst Rev 1(1):CD004143.
- Rossouw JE, Anderson GL, Prentice RL, et al (2002). Risks and benefits of estrogen plus progestin in healthy postmenopausal women: principal results from the Women's Health Initiative randomized controlled trial JAMA 288(3):321-333.
- Boardman HMP, Hartley L, Eisinga A, et al (2015). Hormone therapy for preventing cardiovascular disease in post-menopausal women Cochrane Database Syst Rev 2015(3):CD002229.
- Vinogradova Y, Coupland C, Hippisley-Cox J (2019). Use of hormone replacement therapy and risk of venous thromboembolism: nested case-control studies using the QResearch and CPRD databases BMJ 364:k4810.
- Shumaker SA, Legault C, Rapp SR, et al (2003). Estrogen plus progestin and the incidence of dementia and mild cognitive impairment in postmenopausal women: the Women's Health Initiative Memory Study: a randomized controlled trial JAMA 289(20):2651-2662.
- Pourhadi N, Mørch LS, Holm EA, et al (2023). Menopausal hormone therapy and dementia: nationwide, nested case-control study BMJ 381:e072770.
- Chlebowski RT, Anderson GL, Aragaki AK, et al (2020). Association of menopausal hormone therapy with breast cancer incidence and mortality during long-term follow-up of the Women's Health Initiative randomized clinical trials JAMA 324(4):369-380.
- Basaria S, Coviello AD, Travison TG, et al (2010). Adverse events associated with testosterone administration N Engl J Med 363(2):109-122.
- Xu L, Freeman G, Cowling BJ, Schooling CM (2013). Testosterone therapy and cardiovascular events among men: a systematic review and meta-analysis of placebo-controlled randomized trials BMC Med 11:108.
- Lincoff AM, Bhasin S, Flevaris P, et al (2023). Cardiovascular safety of testosterone-replacement therapy N Engl J Med 389(2):107-117.
- Hudson J, Cruickshank M, Quinton R, et al (2022). Adverse cardiovascular events and mortality in men during testosterone treatment: an individual patient and aggregate data meta-analysis Lancet Healthy Longev 3(6):e381-e393.
- Saso S, Barcroft JF, Kasaven LS, et al (2025). An umbrella review of meta-analyses regarding the incidence of female-specific malignancies after fertility treatment Fertil Steril 123(3):506-519 (published online 2024).
- Berntsen S, Söderström-Anttila V, Wennerholm UB, et al (2019). The health of children conceived by ART: 'the chicken or the egg?' Hum Reprod Update 25(2):137-158.
- Hart R, Norman RJ (2013). The longer-term health outcomes for children born as a result of IVF treatment: Part I, general health outcomes Hum Reprod Update 19(3):232-243.
- Zhang S, Luo Q, Meng R, Yan J, Wu Y, Huang H (2024). Long-term health risk of offspring born from assisted reproductive technologies J Assist Reprod Genet 41(3):527-550.
- Shamseer L, Sampson M, Bukutu C, et al (2015). CONSORT extension for reporting N-of-1 trials (CENT) 2015: explanation and elaboration BMJ 350:h1793.
- Precision Analytical Inc (company document) (2026). Terms and conditions