Menstrual Phase
The cycle begins with menstruation — the shedding of the uterine lining. Oestrogen and progesterone are at their lowest, which is why many women notice low mood, fatigue, and reduced motivation around their period.
Women's health guide
Understand your hormones with expert private blood testing. From menstrual cycles to menopause and PCOS - discover what your body is telling you and take control.
Last reviewed: April 2026 · Produced by Daniel Snow, BSc (Hons) · Medically reviewed by The Livewell Syndicate clinical team
Hormones govern almost every aspect of how a woman feels, functions, and ages. From the energy you have on a Monday morning to the quality of your sleep, your monthly cycle, your weight, and your mood — your endocrine system is quietly orchestrating it all.
Yet for millions of women in the UK, hormonal imbalances go undetected for years. Symptoms are dismissed as stress, ageing, or lifestyle when in fact they reflect measurable, correctable shifts in biochemistry that a targeted private blood test can identify with precision.
This guide explains how the key female hormones work, what happens when they fall out of balance, and how advanced private blood testing gives you the clinical insight to take meaningful action at every stage of life.
The endocrine system is a network of glands distributed throughout the body — including the ovaries, thyroid, adrenal glands, pituitary, and pancreas — each producing chemical messengers known as hormones. These hormones travel through the bloodstream and deliver instructions to organs and tissues, regulating everything from your metabolic rate and reproductive function to your stress response and bone density.
In women, the endocrine system is particularly dynamic. Hormonal concentrations shift across the monthly cycle, across decades of reproductive life, and through the significant physiological transition of menopause. Understanding these shifts — and detecting when they deviate from healthy norms — is the foundation of modern women's preventative healthcare.
Private blood testing makes this understanding actionable. Rather than waiting for symptoms to become severe enough to prompt a GP visit, regular hormonal profiling allows women to identify imbalances early, track trends over time, and take clinically informed steps to restore and maintain balance.
The menstrual cycle is far more than a monthly biological inconvenience. It is one of the body's most sensitive barometers of overall hormonal health. The NHS describes the average cycle as spanning approximately 28 days, though significant variation exists — and deviation from 28 days is not inherently abnormal.
The cycle is governed by a tightly orchestrated sequence of four hormonal phases.
The cycle begins with menstruation — the shedding of the uterine lining. Oestrogen and progesterone are at their lowest, which is why many women notice low mood, fatigue, and reduced motivation around their period.
Overlapping with menstruation, the pituitary releases FSH, signalling the ovaries to mature a follicle. Rising oestrogen rebuilds the uterine lining and typically lifts energy, cognitive clarity, and mood.
A surge in LH — triggered by peak oestrogen — causes the mature follicle to release an egg. This is the most fertile point of the cycle. LH can be measured via blood test as a precise indicator of ovulatory function.
The corpus luteum secretes progesterone to prepare the uterine lining. If fertilisation does not occur, hormones fall sharply and the cycle resets. This drop drives PMS; severe, cyclical symptoms may indicate PMDD.
The hormonal drop in the late luteal phase is the primary driver of premenstrual syndrome (PMS). When symptoms are severe and cyclically debilitating, the condition is classified as Premenstrual Dysphoric Disorder (PMDD) — a diagnosable clinical condition responsive to both lifestyle and pharmacological intervention when properly identified.
While cycle-to-cycle variation is normal, significant and persistent irregularity warrants investigation. Several well-evidenced factors are known to disrupt the hormonal signalling that regulates the cycle.
Chronic psychological stress activates the hypothalamic-pituitary-adrenal (HPA) axis, elevating cortisol and suppressing the pulsatile release of GnRH — the master reproductive hormone — which in turn disrupts FSH and LH secretion. Higher perceived stress correlates with increased rates of cycle disruption, dysmenorrhoea, and premenstrual symptoms.
Inadequate caloric intake relative to energy expenditure — whether through dieting, disordered eating, or intensive athletic training — suppresses reproductive hormone output and can result in menstrual irregularity, amenorrhoea, and long-term consequences for bone health. This mechanism is not limited to athletes; any significant caloric deficit can produce similar hormonal suppression.
Certain prescribed medications are documented to affect menstrual regularity. Antidepressant use — particularly serotonin reuptake inhibitors — has been associated with cycle irregularity, menorrhagia, and amenorrhoea. Some cardiac medications can also affect menstrual bleeding. Women experiencing new or worsening irregularity after starting any medication should discuss this with their prescribing clinician.
Understanding why your cycle is disrupted — not just that it is disrupted — requires targeted investigation. A comprehensive hormonal blood panel, interpreted alongside a detailed clinical history, provides the most diagnostically useful picture.
Polycystic Ovary Syndrome (PCOS) is one of the most prevalent endocrine disorders affecting women of reproductive age, with an estimated global prevalence of 6–13% depending on diagnostic criteria. Despite its prevalence, it remains significantly underdiagnosed, with many women waiting years between symptom onset and formal diagnosis.
PCOS is characterised by excess androgen production. Elevated androgens disrupt the normal maturation and release of eggs, causing follicles to accumulate in the ovaries rather than completing ovulation. Insulin resistance plays a central mechanistic role: excess circulating insulin stimulates the ovaries to produce additional androgens, creating a self-reinforcing cycle of hormonal disruption with significant long-term metabolic implications.
PCOS presents differently across individuals, which is one reason it is so frequently missed. Common features include:
Diagnosis is defined by the Rotterdam Criteria, which require at least two of: irregular or absent ovulation, clinical or biochemical evidence of elevated androgens, and polycystic ovarian morphology on ultrasound. A blood panel is an essential component of the diagnostic workup, not a replacement for clinical assessment.
| Biomarker | Relevance to PCOS |
|---|---|
| Total and free testosterone | Identifies androgen excess — the biochemical hallmark of PCOS |
| SHBG (Sex Hormone-Binding Globulin) | Low SHBG amplifies the biological effect of circulating androgens |
| LH and FSH | An elevated LH:FSH ratio is characteristic of PCOS |
| Fasting insulin and glucose | Identifies insulin resistance before progression to prediabetes |
| HbA1c | Long-term blood sugar average; assesses metabolic risk |
| Prolactin and TSH | Rules out other hormonal conditions that mimic PCOS symptoms |
| AMH (Anti-Müllerian Hormone) | Typically elevated in PCOS, reflecting the increased follicle pool |
Early identification through blood testing enables timely dietary, lifestyle, and clinical interventions that can significantly reduce the long-term metabolic and reproductive consequences of PCOS.
Menopause marks the point at which a woman has experienced 12 consecutive months without a menstrual period — the permanent end of ovarian reproductive function. In the UK, this typically occurs between the ages of 45 and 55. However, the hormonal transition begins considerably earlier in perimenopause — often the most challenging phase to navigate without clinical guidance.
During perimenopause, the ovaries produce oestrogen in an increasingly erratic pattern. This hormonal volatility — rather than simple oestrogen decline — drives many of the most disruptive symptoms:
Perimenopause is primarily a clinical diagnosis, but blood testing provides important supporting evidence — particularly in women under 45. Key markers include FSH (consistently elevated above 30 IU/L on two tests at least six weeks apart supports diagnosis when interpreted with symptoms), oestradiol, and AMH as an early signal of declining ovarian reserve.
Oestrogen plays a protective role in cardiovascular health, bone mineral density, and cognitive function. Following menopause, cardiovascular risk increases significantly and bone mineral density declines at an accelerated rate. Regular blood testing — including bone turnover markers, lipid profiles, inflammatory markers, and hormonal panels — provides the data needed to monitor and mitigate these risks.
The thyroid gland regulates metabolic rate, cardiovascular function, body temperature, mood, and reproductive health. Women are disproportionately affected by thyroid disorders — hypothyroidism affects approximately 2% of women, with a further estimated 5% having subclinical hypothyroidism. Symptoms overlap substantially with depression, anaemia, perimenopause, and anxiety, contributing to frequent diagnostic delay.
The most common cause in the UK is Hashimoto's thyroiditis. Thyroid antibodies (TPOAb and TgAb) can be elevated for years before TSH becomes abnormal — meaning antibody testing is essential for early detection yet is frequently omitted from standard NHS panels.
The most common cause is Graves' disease. TSH receptor antibodies (TRAb) are a specific marker for this diagnosis.
NHS standard thyroid testing typically measures TSH alone. While TSH is an important marker, it does not provide a complete picture — particularly for women whose TSH falls within the reference range but symptoms persist.
| Marker | What It Adds |
|---|---|
| Free T4 (thyroxine) | The primary hormone secreted by the thyroid gland |
| Free T3 (triiodothyronine) | The biologically active form; some individuals have impaired T4-to-T3 conversion despite normal TSH and T4 |
| TPOAb and TgAb | Detects autoimmune thyroid disease before TSH becomes abnormal |
| TRAb | Specific marker for Graves' disease in suspected hyperthyroidism |
The adrenal glands produce cortisol, DHEA-S, and adrenaline — hormones with significant influence on energy, mood, weight regulation, immune function, and broader hormonal balance.
Acute cortisol release is a healthy survival mechanism. In sustained stress, chronic cortisol elevation can disrupt sleep, promote visceral fat accumulation, suppress immune competence, and interfere with reproductive hormone balance — cortisol competes with progesterone at receptor level, and chronically elevated cortisol can suppress the LH surge necessary for ovulation.
Chronically elevated cortisol also impairs the peripheral conversion of T4 to active T3, potentially contributing to hypothyroid-like symptoms even when standard thyroid function tests appear normal.
DHEA-S is a marker of adrenal reserve that declines with age and can fall sharply in response to chronic stress. In women, DHEA-S contributes to peripheral production of oestrogen and testosterone. Measuring DHEA-S alongside cortisol provides a more clinically complete picture of adrenal function than either marker in isolation.
The table below summarises the core hormonal biomarkers included in a comprehensive women's health blood panel, together with what each marker reveals and why it matters clinically.
| Biomarker | What It Measures | Why It Matters |
|---|---|---|
| Oestradiol (E2) | Primary active oestrogen | Cycle regulation, bone density, cardiovascular protection, mood stability |
| Progesterone | Luteal phase hormone | Cycle balance, PMS/PMDD severity, fertility support, sleep quality |
| FSH | Pituitary signal to ovaries | Ovarian reserve; significantly elevated in perimenopause and menopause |
| LH | Triggers ovulation | LH:FSH ratio is diagnostically useful in PCOS; confirms ovulatory function |
| Testosterone (total & free) | Androgen level | Energy, libido, muscle maintenance; elevated in PCOS |
| SHBG | Binds and regulates sex hormones | Determines biologically active testosterone; central to PCOS assessment |
| AMH | Ovarian egg reserve | Fertility assessment; tracks progression toward menopause |
| TSH, Free T3, Free T4 | Thyroid function | Metabolic rate, weight, energy, mood, temperature regulation |
| TPOAb / TgAb | Thyroid autoimmunity markers | Identifies Hashimoto's thyroiditis before TSH becomes abnormal |
| Cortisol | Adrenal stress response | Energy regulation, sleep quality, immune function, weight distribution |
| DHEA-S | Adrenal reserve and hormonal precursor | Declines with age and chronic stress; contributes to sex hormone production |
| Prolactin | Pituitary hormone | Elevated in conditions disrupting ovulation; assessed as part of PCOS workup |
| Fasting insulin and HbA1c | Blood sugar and insulin sensitivity | Identifies insulin resistance in PCOS; assesses long-term metabolic risk |
| Vitamin D | Hormonal co-factor | Bone density, immune function, mood regulation, oestrogen metabolism |
A comprehensive women's hormone panel typically includes oestradiol, progesterone, testosterone (total and free), FSH, LH, SHBG, AMH, prolactin, TSH, free T3, free T4, thyroid antibodies (TPOAb and TgAb), cortisol, DHEA-S, fasting insulin, HbA1c, and vitamin D. The specific markers recommended depend on your age, symptoms, cycle regularity, and clinical history.
For women who are still menstruating, hormone tests should ideally be timed to specific points in the cycle. Oestradiol and FSH are most informative when tested on days 2–5 of the cycle (the early follicular phase). Progesterone is best measured around day 21 — the mid-luteal phase — to confirm whether ovulation has occurred. A clinician can advise on the most appropriate timing based on your specific symptoms and cycle pattern.
Blood tests support but do not independently diagnose perimenopause. A consistently elevated FSH (typically above 30 IU/L on two separate tests at least six weeks apart), combined with declining oestradiol and characteristic symptoms, provides strong evidence of the perimenopausal transition. Perimenopause can begin several years before the final menstrual period, and symptoms frequently precede measurable changes in blood markers.
No. PCOS is diagnosed using the Rotterdam Criteria, which require at least two of the following: irregular or absent ovulation, elevated androgens (biochemically or clinically), and polycystic ovarian morphology on ultrasound. A blood panel is an essential part of the PCOS workup, but clinical assessment — and often pelvic ultrasound — is required alongside laboratory results for a formal diagnosis.
Total testosterone measures all testosterone in the blood, including the large fraction bound to proteins (primarily SHBG) that is biologically inactive. Free testosterone measures only the unbound fraction available to act on tissue receptors. In women with low SHBG — common in PCOS and insulin resistance — free testosterone can be elevated even when total testosterone appears within the normal range, making both measurements clinically important.
For many women, yes — particularly when symptoms persist. TSH alone does not capture how much active thyroid hormone (free T3) is reaching your cells, nor does it detect early-stage autoimmune thyroid disease. Some women have normal TSH but impaired T4-to-T3 conversion, or elevated thyroid antibodies that predict future thyroid dysfunction. A comprehensive private panel including free T3, free T4, TPOAb, and TgAb provides a complete picture that TSH alone cannot.
This depends on age, symptoms, and circumstances. Women in their 30s tracking fertility, those experiencing perimenopausal symptoms, and those managing conditions such as PCOS or thyroid disease typically benefit from annual or biannual retesting to monitor trends and assess the impact of any interventions. A comprehensive baseline panel is valuable at any stage of adult life.
Yes — this is well-evidenced. Chronic stress elevates cortisol, which suppresses the hormonal signalling that regulates ovulation. Similarly, physical or nutritional stress — such as insufficient caloric intake relative to energy expenditure — can suppress reproductive hormone output entirely.
Take the next step
Whether you are managing unexplained fatigue, irregular periods, the transition into perimenopause, a suspected thyroid condition, or simply want a clear, evidence-based picture of where your hormones stand — a targeted private blood panel provides the clinical answers your body deserves.