Women's Health · Article 34
Menopause
and Perimenopause
A natural transition that affects every woman — what it is, what it does to the body, and what the evidence says about managing it.
Dr Paul · Retired NHS GP · 20+ years NHS experience
Menopause is a natural biological event that every woman experiences — the point at which the ovaries stop releasing eggs and oestrogen (the primary female sex hormone) production falls significantly. It is defined as twelve consecutive months without a menstrual period. What comes before that point is perimenopause (the transitional phase, often lasting several years), and what comes after is postmenopause (the rest of life beyond that point).
In the UK, the average age at which menopause occurs is 51, with most women reaching it between the ages of 45 and 55.[1] But the transition typically begins earlier than that — perimenopause usually starts in the mid-to-late 40s, with hormone levels beginning to fluctuate unpredictably before periods stop altogether.[1]
Perimenopause — the transition phase
Perimenopause (from the Greek peri, meaning "around") is the phase leading up to the final period. During this time, the ovaries begin producing less oestrogen and progesterone (the hormone that prepares the womb lining for pregnancy), but not consistently — levels fluctuate, sometimes quite dramatically, from month to month and even day to day. Periods may become irregular — shorter, longer, heavier, lighter, or more widely spaced. Menopause-associated symptoms often begin during this phase, sometimes before any change in periods is noticed at all.
Perimenopause can last anywhere from a few months to over a decade. There is no reliable way to predict its duration for any individual woman. It ends once twelve months have passed without a period, at which point menopause is confirmed retrospectively.
Postmenopause
Postmenopause refers to all the years that follow. Oestrogen levels stabilise at a lower level — not zero, but significantly reduced compared to reproductive years. For many women, the more acute vasomotor symptoms (hot flushes and night sweats — see Key Terms below) improve over time. But the lower oestrogen environment continues to have effects on bone density, cardiovascular risk, and genitourinary health (see Section 2).
Surgical and medically induced menopause
Menopause can also occur as a result of surgery (bilateral oophorectomy — surgical removal of both ovaries) or certain medical treatments, including chemotherapy and radiotherapy directed at the pelvic area. In these cases, menopause is immediate rather than gradual, and symptoms are often more abrupt and severe, because the hormone change happens suddenly rather than over several years.
Premature ovarian insufficiency and early menopause
Premature ovarian insufficiency (POI — reduced or absent ovarian function) affects around 1 in 100 women and occurs before age 40.[2] Early menopause (between ages 40 and 44) affects between 3% and 8% of women.[3] Both carry specific long-term health implications — particularly for cardiovascular health and bone density — because oestrogen deficiency occurs at a younger age than expected. NICE NG23 recommends that women with POI be offered HRT (hormone replacement therapy — see Key Terms below) and continued on it until at least the average age of natural menopause, unless there is a contraindication (a medical reason not to use it).
Perimenopause
The transitional phase leading up to menopause — when oestrogen begins to fall and symptoms often start, but periods have not yet stopped for twelve months.
Menopause
The point defined as twelve consecutive months without a menstrual period. Diagnosed retrospectively — it can only be confirmed once the twelve months have passed.
Oestrogen
The primary female sex hormone, produced mainly by the ovaries. Responsible for regulating the menstrual cycle and influencing bone density, cardiovascular health, mood, and cognition.
Progesterone
A female sex hormone that prepares the womb lining for pregnancy. In HRT, a progestogen (synthetic or body-identical form of progesterone) is added to protect the womb lining in women who have not had a hysterectomy.
Vasomotor symptoms
Symptoms caused by changes in blood vessel activity — including hot flushes (sudden intense heat, usually starting in the chest or face) and night sweats. The most commonly reported symptoms of perimenopause and menopause.
HRT (Hormone Replacement Therapy)
Treatment that replaces the oestrogen (and, in women with an intact womb, progesterone) that the ovaries are no longer producing. Available in different forms — patches, gels, sprays, tablets, and implants.
Transdermal
Delivered through the skin — for example, an oestrogen patch or gel. Transdermal oestrogen enters the bloodstream without passing through the liver first, which avoids the increased blood clot risk associated with oral (swallowed) oestrogen tablets.
Premature Ovarian Insufficiency (POI)
Reduced or absent ovarian function occurring before the age of 40. Distinct from natural menopause because it occurs significantly earlier than expected and carries additional long-term health implications.
Genitourinary syndrome of menopause (GSM)
A cluster of symptoms affecting the vagina and urinary tract caused by falling oestrogen levels — including vaginal dryness, discomfort during sex, and urinary symptoms such as urgency or recurrent infections.
FSH (Follicle-Stimulating Hormone)
A hormone produced by the pituitary gland in the brain. FSH levels rise when the ovaries are producing less oestrogen — which is why an FSH blood test can sometimes help confirm menopause in women under 45 where the diagnosis is unclear.
13M
women in the UK are currently perimenopausal or menopausal — approximately one third of the entire female population.
[4]
~80%
of women going through menopause experience vasomotor symptoms including hot flushes and night sweats, according to NICE NG23.
[5]
1 in 100
women experience premature ovarian insufficiency — menopause before age 40 — which carries additional long-term implications for bone and heart health.
[2]
1 in 3
women aged 50 and over will experience a fragility fracture (a bone fracture caused by a minor fall or force) during their remaining lifetime due to postmenopausal bone density loss.
[6]
Vasomotor symptoms — hot flushes and night sweats
Hot flushes are the most recognised symptom of menopause — a sudden sensation of intense warmth, usually beginning in the chest and rising to the face and neck, often accompanied by reddening of the skin and followed by sweating and chills. Night sweats are the same phenomenon occurring during sleep, often waking women repeatedly and significantly disrupting sleep quality. Around 80% of women experience these symptoms to some degree.[5] For many women, they are mild and manageable. For others, they are severe — frequent, disabling, and substantially affecting quality of life and the ability to work.
Sleep, mood, and cognition
Sleep disruption from night sweats is one of the most commonly reported impacts of perimenopause. Sustained poor sleep has downstream effects on mood, concentration, memory, and emotional resilience. Many women also report cognitive symptoms directly — commonly described as brain fog, difficulty finding words, and a sense that memory and mental sharpness have reduced. Low mood, anxiety, and irritability are also frequently reported, and appear to have both a hormonal basis (oestrogen has direct effects on mood-regulating neurotransmitters — chemical messengers in the brain) and a secondary basis through sleep deprivation and the cumulative impact of persistent symptoms.
Genitourinary syndrome of menopause (GSM)
Falling oestrogen levels affect the tissues of the vagina, vulva, and urinary tract — causing them to become thinner, drier, and more fragile. This can lead to vaginal dryness, itching, discomfort or pain during sexual intercourse, and urinary symptoms including urgency, frequency, and a greater tendency to urinary tract infections (UTIs — bladder infections). Unlike vasomotor symptoms, which often improve with time, GSM tends to persist and can worsen without treatment. It is substantially undertreated — many women are unaware that effective, safe local treatments exist, and many are reluctant to raise it.
Bone density
Oestrogen plays a critical role in maintaining bone density — the structural strength of bones. When oestrogen falls sharply at menopause, bone is lost at an accelerated rate. Research published in the New England Journal of Medicine found that mean annual bone mineral density loss in postmenopausal women was 1.9%.[6] Over time, this loss accumulates into osteopenia (reduced bone density, see Key Terms) and osteoporosis (low bone mass — bone mineral density T-score of −2.5 or below — increasing the risk of fragility fractures — fractures caused by forces that would not break a healthy bone). One in three women aged 50 and over will experience a fragility fracture during their remaining lifetime.[6]
Cardiovascular health
Oestrogen has a protective effect on the cardiovascular system — it supports healthy blood vessel function and influences cholesterol profiles. After menopause, this protection diminishes, and cardiovascular risk rises. Women's risk of heart disease increases significantly in postmenopause, and by older age, women's cardiovascular disease rates converge with — and in some conditions exceed — those of men. The timing of any hormonal intervention matters here, which is discussed in Section 3.
Work and quality of life
Menopause is now recognised as a significant occupational health issue. Women aged 45–55 represent the fastest-growing group in the UK workforce. Severe symptoms affect the ability to concentrate, maintain performance, manage work relationships, and in some cases lead women to reduce hours, turn down promotion, or leave employment altogether. The combined impact of vasomotor symptoms, poor sleep, cognitive symptoms, and mood change can be substantial — and for many women, deeply isolating, partly because the connection between what they are experiencing and menopause goes unrecognised for years.
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A slide-by-slide visual overview of this article. Use the ← → arrow keys on your keyboard, or tap the dots at the bottom of the panel to move between slides.
📱 TikTok · Instagram · #menopause · 2026
758.9K
#menopause videos on TikTok · TikTok tag page, 2026
93%
of major UK HRT social media content creators had conflicts of interest
563K
#perimenopause videos on TikTok · TikTok tag page, 2026
A BMJ study published August 2025 analysed 180 top UK social media posts about HRT across TikTok, Instagram, YouTube, Facebook, X, and Google. 93% of major content creators had direct or indirect conflicts of interest — through private practice, pharmaceutical funding, or retail products. The #menopause hashtag has 758.9K videos on TikTok alone.
Bikha A et al · BMJ · August 2025 · TikTok tag page data, 2026
👆 Tap any card to reveal what the evidence shows
✕ Myth 1 of 5"HRT causes breast cancer — it's too dangerous to take"
📱 TikTok · 758.9K #menopause videos · TikTok tag page, 2026 · HRT fear content among most-circulated menopause claims
Tap to see the evidence →
✓ Reality4 per 1,000
extra breast cancer cases over 5 years of combined HRT use — the same additional risk as the contraceptive pill
The fear stems from a misrepresented 2002 WHI study of older women on one specific formulation. The FDA removed its longstanding black-box cancer warning in November 2025, reflecting updated evidence. For oestrogen-only HRT, there is little or no increased breast cancer risk.
NICE NG23 · Cancer Research UK · BCRF, February 2026 · Tap to flip back
✕ Myth 2 of 5"Bioidentical hormones are safer and more natural than prescribed HRT"
📱 TikTok · Instagram · 758.9K #menopause videos · TikTok tag page, 2026 · bioidentical claims widespread among wellness influencers
Tap to see the evidence →
✓ Reality0
clinical trials showing compounded bioidentical hormones are safer or more effective than regulated HRT
There are FDA-approved bioidentical formulations — these are regulated and carry the same risk-benefit profile as conventional HRT. Compounded versions are not subject to the same oversight, can have inconsistent dosing, and have not been tested in randomised trials. Being plant-derived does not make them safer.
NICE NG23, updated November 2024 · BJGP · November 2019 · Tap to flip back
✕ Myth 3 of 5"Menopause weight gain is inevitable and there's nothing you can do"
📱 TikTok · 563K #perimenopause videos · TikTok tag page, 2026 · weight gain fatalism widely circulating
Tap to see the evidence →
✓ RealityLess
visceral fat (abdominal fat around organs) in HRT users vs non-users — and better preservation of lean muscle mass
HRT does not cause weight gain and may reduce abdominal fat accumulation. Metabolic changes around menopause do make weight management harder — but they are not inevitable. Exercise, particularly resistance training, and evidence-based nutrition are effective. HRT is symptom treatment, not a weight-loss drug.
NICE NG23, updated November 2024 · NHS Inform · Tap to flip back
✕ Myth 4 of 5"Natural supplements can replace HRT for menopause symptoms"
📱 TikTok · 758.9K #menopause videos · TikTok tag page, 2026 · supplement promotion among most-viewed menopause content
Tap to see the evidence →
✓ RealityNo
supplement — including black cohosh, red clover, or ashwagandha — has been shown to match HRT for moderate-to-severe vasomotor symptoms
Some supplements may provide modest benefit for mild hot flushes. For moderate or severe symptoms, they are not an evidence-based replacement for HRT. Many are promoted by influencers with financial conflicts of interest — the BMJ 2025 UK study found 93% of major menopause content creators had commercial ties.
NICE NG23 · Bikha A et al · BMJ · August 2025 · Tap to flip back
✕ Myth 5 of 5"Menopause happens suddenly at a fixed age — if your periods are regular, you're not in it yet"
📱 TikTok · 563K #perimenopause videos · TikTok tag page, 2026 · perimenopause awareness gap widely documented
Tap to see the evidence →
✓ Reality40s
when perimenopause typically begins — sometimes earlier — while periods may still be regular
Perimenopause (the transition phase before menopause) can begin in the early 40s and lasts an average of 4–8 years. Symptoms — including sleep disturbance, mood changes, brain fog, and irregular periods — often begin well before periods stop. Menopause is defined as 12 consecutive months without a period. The average age in the UK is 51, but around 1% of women experience it before 40 (premature ovarian insufficiency).
NICE NG23, updated November 2024 · NHS · Tap to flip back
How menopause is identified — the NICE approach
NICE guideline NG23 (updated November 2024) sets out a clear diagnostic framework. For women aged 45 or over who present with vasomotor symptoms (see Key Terms) and changes to their menstrual cycle, perimenopause or menopause is identified clinically — without blood tests.[5] This is important: a normal or low FSH (follicle-stimulating hormone — see Key Terms) result does not rule out perimenopause, because FSH levels fluctuate considerably during the transition.
For women under 45 with suspected perimenopause, NICE recommends measuring FSH on two occasions, at least four to six weeks apart. For women under 40 where POI is suspected, FSH and oestradiol (the main form of circulating oestrogen) should be measured, and referral to a specialist is recommended.
Hormonal contraception and diagnosis: Women taking hormonal contraception (including the pill, implant, injection, or hormonal coil) may have suppressed periods regardless of menopausal status. Identifying menopause in these women requires clinical judgement and is discussed with the prescribing clinician — hormone tests may be unreliable in this context.
Managing symptoms — the main options
Most effective for vasomotor symptoms
HRT — Hormone Replacement Therapy
HRT replaces the oestrogen the ovaries are no longer producing. In women who have not had a hysterectomy (surgical removal of the womb), a progestogen (synthetic or body-identical form of progesterone) is also prescribed to protect the womb lining. NICE NG23 recommends HRT as the most effective treatment for vasomotor symptoms.
[5] It is also effective for GSM, mood symptoms, and bone health.
Non-hormonal · evidence-based
CBT (Cognitive Behavioural Therapy)
Cognitive behavioural therapy — a structured talking therapy that addresses patterns of thinking and behaviour — has an evidence base for reducing the impact of hot flushes and night sweats, and for improving mood and psychological wellbeing. NICE NG23 (2024) explicitly describes CBT as a recommended option alongside HRT, or for women who cannot take or choose not to use hormonal treatment.
[5]
Non-hormonal · newer option
Fezolinetant (Veoza)
Fezolinetant (Veoza) is a neurokinin 3 receptor antagonist — a non-hormonal medication that targets a specific pathway in the brain involved in triggering hot flushes. It was approved by the MHRA (the UK medicines regulator) in 2024. It is an option for women who cannot or prefer not to use HRT.
Localised treatment
Vaginal oestrogen
Topical oestrogen applied directly to the vagina and vulva — available as a cream, pessary, ring, or gel — treats GSM effectively without the systemic absorption of body-wide HRT. NICE NG23 recommends that vaginal oestrogen be offered for urogenital (affecting the urinary tract and genitals) symptoms. It is considered safe for long-term use and can be used alongside or independently of systemic HRT.
HRT — types, routes, and the timing question
HRT is available in several forms and via different routes:
| Type | Who it is for | Common preparations |
| Combined HRT (oestrogen + progestogen) |
Women who still have their womb |
Transdermal (through the skin) patches such as oestradiol (Evorel, Estradot); oestrogen gel or spray; with oral or intrauterine progestogen — for example, micronised progesterone (Utrogestan) or levonorgestrel-releasing IUS (intrauterine system — a small hormone-releasing device fitted inside the womb; brand name Mirena) |
| Oestrogen-only HRT |
Women who have had a hysterectomy |
Oestradiol patches, gel, or spray; oral oestradiol tablets; oestrogen implants |
| Tibolone (Livial) |
Postmenopausal women (not perimenopause) |
Synthetic steroid with oestrogenic, progestogenic, and mild androgenic (testosterone-like) activity |
Transdermal oestrogen (patches, gels, and sprays) does not carry the same increased risk of blood clots (venous thromboembolism, or VTE — a clot in the veins) that is associated with oral oestrogen tablets, because it bypasses first-pass liver metabolism (the initial processing of a drug by the liver after it is swallowed). This is relevant for women who have risk factors for blood clots.
The timing question: Evidence suggests that HRT is most beneficial — particularly in relation to cardiovascular health — when started within ten years of menopause onset, or before age 60. Starting HRT many years after menopause, particularly in women who already have established cardiovascular disease, carries different risk-benefit considerations. This is an individualised clinical discussion, not a blanket rule.
Bone health monitoring
NICE NG23 recommends that women with POI be advised about the risk to bone health and offered DEXA scanning (dual-energy X-ray absorptiometry — a bone density scan) to assess their baseline bone mineral density. For women undergoing natural menopause, risk assessment using tools such as FRAX (Fracture Risk Assessment Tool) helps identify those who would benefit from further assessment or treatment. HRT reduces the rate of postmenopausal bone loss and is recognised as an effective treatment for preventing osteoporosis in women who are symptomatic — bone protection is one of several reasons the conversation about HRT takes place.
Lifestyle factors with evidence
NICE NG23 describes lifestyle factors that support wellbeing through the menopause transition and beyond. Weight-bearing exercise (walking, jogging, resistance training) helps maintain bone density and supports cardiovascular health. Adequate dietary calcium and vitamin D are important for bone health. Reducing alcohol intake and avoiding smoking are relevant to both bone health and breast cancer risk. Regular exercise has a modest evidence base for reducing vasomotor symptom frequency.
Three areas of evidence matter most for understanding menopause management: the effectiveness of HRT for vasomotor symptoms, the relationship between HRT and breast cancer risk, and the impact of menopause on bone health.
Key finding
77%
reduction in hot flush frequency — HRT vs placebo across 21 randomised trials
Maclennan AH et al · Cochrane Database Syst Rev · 2004 · 21 RCTs · n=2,511
HRT is highly effective for vasomotor symptoms
Cochrane Database of Systematic Reviews · 2004 · DOI: 10.1002/14651858.CD002978.pub2 · PMID 15495039
A Cochrane systematic review of 21 randomised controlled trials (studies where participants were randomly assigned to treatment or placebo) involving 2,511 women found that oral HRT reduced hot flush frequency by 77% compared with placebo (an inactive treatment used as a comparator). The reduction in symptom severity was also highly significant. A substantial placebo effect (50.8% reduction with placebo alone) was also observed — underlining the importance of comparing treatments against placebo rather than no treatment. Symptom severity was also significantly reduced compared with placebo.
Key finding
1 in 50
additional cases
of breast cancer in women using combined HRT continuously for 5+ years (ages 50–69), compared with non-users
Collaborative Group on Hormonal Factors in Breast Cancer · The Lancet · 2019 · 108 prospective studies · 100,000+ women with breast cancer
Combined HRT carries a small but real increase in breast cancer risk
The Lancet · 2019 · 394(10204):1159–1168 · DOI: 10.1016/S0140-6736(19)31709-X · PMID 31474332
This large meta-analysis (a study that combines data from multiple studies) of individual participant data from prospective studies covering over 100,000 women with breast cancer found that combined HRT (oestrogen plus daily progestogen) used for 5 or more years is associated with approximately 1 additional breast cancer per 50 users aged 50–69. Oestrogen-only HRT (used by women who have had a hysterectomy) carries a lower risk. Some excess risk persists for more than 10 years after stopping combined HRT. Micronised progesterone (Utrogestan — a body-identical form of progesterone) appears to carry a lower risk than synthetic progestogens. This is one component of an individualised benefit-risk discussion, not a reason to avoid HRT categorically.
Key finding
1.9%
per year
mean annual bone mineral density loss in the postmenopausal period — measured over 15 years of follow-up
Ahlborg HG et al · New England Journal of Medicine · 2003 · 108 women · 15-year follow-up from menopause
Postmenopausal bone loss is measurable, progressive, and clinically significant
New England Journal of Medicine · 2003 · DOI: 10.1056/NEJMoa022464
A 15-year prospective study of 108 women followed from the time of menopause measured bone mineral density (BMD — the amount of mineral per square centimetre of bone) every two years. Mean annual BMD loss was 1.9% — meaning that over a decade, a woman can lose nearly 20% of her bone density from the postmenopausal period alone. Lower postmenopausal oestradiol (circulating oestrogen) levels were associated with greater bone loss. Fractures of the distal radius (wrist) were recorded; women with the lowest BMD had the highest fracture rate. HRT is recognised by NICE NG23 as effective for preventing postmenopausal bone loss.
A note on the Women's Health Initiative: Much of the uncertainty around HRT stems from the Women's Health Initiative (WHI) trial published in 2002, which reported increased risks of breast cancer, heart disease, and stroke with HRT. Subsequent reanalysis showed that the average participant age was 63 — significantly older than the perimenopausal women for whom HRT is typically prescribed — and that many had pre-existing cardiovascular disease. The timing of HRT initiation relative to menopause significantly affects the risk-benefit profile. The current NICE NG23 (2024) guidance reflects this more nuanced understanding.
🔑 Putting it all together
Menopause is a natural biological transition — but one that carries real, measurable health implications that extend well beyond hot flushes and irregular periods. The fall in oestrogen that begins during perimenopause affects bone density, cardiovascular risk, urogenital tissue, sleep, mood, and cognitive function. For many women, the impact is substantial. For some, it is severely disabling. Understanding what is happening and knowing that effective evidence-based treatments exist — hormonal and non-hormonal — is the foundation of informed decision-making.
The HRT debate of the early 2000s caused substantial harm by leading many women to avoid treatment that was appropriate for them. The current evidence, reflected in NICE NG23 (updated November 2024), is more nuanced: HRT, started at the right time for the right woman, carries a benefit-risk profile that for most women with significant symptoms is clearly favourable. The small increased risk of breast cancer with combined HRT is real and deserves honest discussion — but it exists alongside meaningful benefits to quality of life, bone health, and cardiovascular outcomes in the window of opportunity around the menopause transition.
For every woman, the details matter — the type of HRT, the route of administration, the timing, the individual medical history, and what she values. That conversation belongs with a GP or healthcare professional — and it is a conversation that is worth having.
Created and reviewed by Dr Paul — Retired NHS GP · 20+ years in general practice · Retired 2019 · Founder, helf.school.
Read more about Dr Paul →
References
1
NHS. Menopause — Overview. NHS website. Reviewed 2023. Also: The Dudley Group NHS Foundation Trust. Understanding Menopause. Patient Information Leaflet, 2025.
2
NHS. Menopause — Causes. NHS website. Reviewed 2023. Also: UK Parliament House of Commons Library. Support for people experiencing menopausal symptoms. Research Briefing CDP-2021-0078. 2021.
3
National Institute for Health and Care Excellence. Menopause: identification and management — Scope. NICE guideline NG23. Updated November 2024. [Prevalence figures for early menopause and premature ovarian insufficiency cited from the NG23 scope document.]
4
Wellbeing of Women, cited in NHS England. Menopause in the workplace. NHS England Citizen Space consultation. Also: UK Parliament House of Commons Library. CDP-2021-0078. 2021.
5
National Institute for Health and Care Excellence. Menopause: identification and management. NICE guideline NG23. Originally published November 2015; updated November 2024.
6
Ahlborg HG, Johnell O, Turner CH, Rannevik G, Karlsson MK. Bone loss and bone size after menopause. New England Journal of Medicine. 2003;349(4):327–334. DOI: 10.1056/NEJMoa022464. Also: Geelong Osteoporosis Study (Pasco JA et al, PMC 12137504) confirming 1 in 3 fracture figure.
7
Maclennan AH, Broadbent JL, Lester S, Moore V. Oral oestrogen replacement therapy versus placebo for hot flushes. Cochrane Database of Systematic Reviews. 2004;(4):CD002978. DOI: 10.1002/14651858.CD002978.pub2. PMID: 15495039.
8
Collaborative Group on Hormonal Factors in Breast Cancer. Type and timing of menopausal hormone therapy and breast cancer risk: individual participant meta-analysis of the worldwide epidemiological evidence. The Lancet. 2019;394(10204):1159–1168. DOI: 10.1016/S0140-6736(19)31709-X. PMID: 31474332.