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Menopause is defined as the permanent cessation of menstrual periods. However, the symptoms of menopause can begin before the cessation of menses and extend over several years.1

 

Perimenopause, the transition from the reproductive period to the first year postmenopause, is associated with increasing symptom burden. This is due to the neurochemical changes in the central nervous system, which are associated with Vasomotor Symptoms (VMS), sleep disorders, and depression.1

 

Other symptoms can include changes in body shape related to cardiometabolic changes, musculoskeletal alterations, skin and urogenital atrophy, sexual dysfunction, osteoporosis, and sarcopenia.1

 

The symptoms of menopause not only have a significant effect on quality of life, they also have been associated with the onset of chronic conditions—serving as predictors of future health risks.1

The most bothersome symptoms of menopause—and the most common reason women seek medical care during the menopausal transition—are hot flushes and night sweats, also know as Vasomotor Symptoms.2 Hot flushes are characterised by a sudden intense sensation of heat in the upper body, particularly the face, neck, and chest. Episodes of VMS typically last 1 to 5 minutes, and can be accompanied by perspiration, chills, anxiety, and heart palpitations. However, individual experiences of VMS vary.3

Oestrogen declines during menopause. Among the effects of this decline are vaginal atrophy, ageing of skin, osteoporosis, and VMS.1.4.6

In the case of VMS, we now know that during menopause, less oestrogen reaches the oestrogen receptors of kisspeptin/neurokinin B/dynorphin (KNDy) neurons, which are located in the temperature control centre of the hypothalamus. The reduction in oestrogen alters the activity of the KNDy neurons, and that altered activity is one of the causes of VMS.4,6

VMS are physiological symptoms associated with menopause.3

 

In the temperature control centre in the hypothalamus:

  • Neurokinin B (NKB) and oestrogen modulate KNDy neurons in a delicate balance, contributing to body temperature regulation. KNDy neurons are stimulated by NKB and inhibited by oestrogen6-8
  • Through the menopausal transition, oestrogen declines, disrupting the balance with NKB6,7,9
  • Unopposed, NKB signalling causes heightened KNDy neuronal activity, which leads to hypertrophy of KNDy neurons and altered activity in the temperature control centre6,7,9
  • As a result, the temperature control centre triggers heat dissipation effectors that cascade into hot flushes and night sweats—VMS6,9

Watch a hot flush in action

Studies have shown that the frequency and severity of VMS may be used as a predictor of chronic diseases in the future, such as cognitive impairment, cardiovascular disease, and osteoporosis.10

Even though hormone therapy (HT) has long been the standard of care, diminished oestrogen is not the only cause of VMS.4,5

 

[Current treatment classes for hot flushes and night sweats include HT and SSRI.] Other treatment strategies include over-the-counter remedies like supplements and herbs. Each of these options has varying levels of efficacy and safety.2

 

[SSRI=selective serotonin reuptake inhibitor.]

Up to 80% of women are affected by VMS during the menopausal transition.3 VMS last for a median duration of 7.4 years, and women living with VMS reported a negative impact on sleep (82%), mood (69%), concentration (69%), energy (63%), sexual activity (41%), work (46%), social activities (44%), and leisure activities (48%).11,12

Not all women realise that VMS are a medical condition worthy of discussion; therefore, many go undiagnosed or untreated.13,14 Having a productive dialogue is crucial in helping women impacted by VMS. Studies show that women want to have open and honest conversations about menopause symptoms and treatment options with their doctor.13


VMS in her words
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VMS in her words

MAT_ABC_NON_2023-00086

Burden of VMS brochure 4 column image

Diagnosis

Find out more about the impacts that VMS have on women. Oestrogen and neurokinin B (NKB) modulate KNDy neurons in a delicate balance, contributing to body temperature regulation.

Oestrogen and neurokinin B (NKB) modulate KNDy neurons in a delicate balance, contributing to body temperature regulation. KNDy neurons are stimulated by NKB and inhibited by oestrogen.1,2,3

  • Padilla SL, Johnson CW, Barker FD, Patterson MA, Palmiter RD.
  • A neural circuit underlying the generation of hot flushes. Cell Rep 2018;24(2):271-7.
  • 1.Krajewski-Hall SJ, Blackmore EM, McMinn JR, Rance NE.
  • 2.Krajewski-Hall SJ, Blackmore EM, McMinn JR, Rance NE.
  • 3.Krajewski-Hall SJ, Blackmore EM, McMinn JR, Rance NE.
VMS in her words

Kicker

MAT-AU-NON-2023-00029 [08/23]

Burden of VMS brochure

Find out more about the impacts that VMS have on women

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