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Bioinformatics analysis of key genes involved in perimenopausal SCD and SCD-MCI-AD coactivation and exploration of their potential mechanisms of action

Bioinformatics analysis of key genes involved in perimenopausal SCD and SCD-MCI-AD coactivation and exploration of their potential mechanisms of action

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400089079
Enrollment
Unknown
Registered
2024-09-01
Start date
2024-09-01
Completion date
Unknown
Last updated
2024-09-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Subjective cognitive decline in perimenopause

Interventions

Healthy control group:None
Perimenopausal SCD group:None

Sponsors

the Affiliated Hospital of Guizhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
50 Years to 55 Years

Inclusion criteria

Inclusion criteria: (1) Perimenopausal women who are in the early (-2) to early (+1a) menopausal transition period according to the Stages of Reproductive Aging +10 (STRAW+10). Early menopausal transition is marked by an increase in menstrual cycle length variability, which is defined as a persistent change in the difference between consecutive cycle lengths of 7 days or more. Persistence is defined as recurrence within 10 cycles after the first occurrence of cycle length variation. Late menopausal transition (-1 stage) Late menopausal transition is marked by the presence of menopause of 60 d or more. The +1a stage of early late menopause is 1 year after the final menstrual period (FMP), which corresponds to the end of perimenopause. Subjects must be able to give informed consent and comply with and complete the study procedures. Subjects were required to complete: 1) Self-Depression Scale (SDS); 2) Memory: Auditory Word Learning Test (AVLT-H); 3) Executive Function: Shape Shifting Tests A & B (STT-A&B) and Montreal Cognitive Assessment (MoCA); 4) Functional Activities Questionnaire (FAQ); and 5) Clinical Dementia Rating (CDR), with normal scores on all of the above scales. and the scores of the above scales are within normal values. (4) Secondary school education or above. ? Age (50-55 years old). (6) BMI (18.5-23.9 kg/m2 ). ?No hormone therapy.

Exclusion criteria

Exclusion criteria: ? Other conditions that may impair cognition or confound assessment: 1) Common brain disorders including neurodegenerative disorders such as Alzheimer's disease, Parkinson's disease, cerebrovascular disease, inflammatory encephalopathies, and head trauma. 2) Serious primary conditions such as severe cardiovascular (myocardial infarction, unstable angina, hospitalization for congestive heart failure, bypass surgery or angioplasty (coronary or carotid artery) transient ischemic attack).3) History of malignancy, carbon monoxide poisoning, and general anesthesia as suggested by current or medical history. ? Patients with neuropsychiatric dysfunction (e.g., dementia, Parkinson's disease, cerebrovascular disease, depressive disorders, mania, mild cognitive dysfunction, etc.). ?People who use medications to treat neurological conditions, such as antidepressants. (iv) Other diseases related to cognition include metabolic diseases, endocrine diseases (e.g., thyroid dysfunction), hypertension, heart disease, anemia, liver disease, kidney disease, infectious diseases, nutritional deficiencies, and diabetes mellitus. ? Those who have never given birth. ? Alcoholics and drug addicts.

Design outcomes

Primary

MeasureTime frame
messenger RNA(mRNA);miRNA;Long non-coding RNA(lncRNA);circRNA;BMI;nation;habit;

Secondary

MeasureTime frame
age;hypertension;pregnancy and childbirth;sex hormone test;liver and kidney function;blood lipid;thyroid function;gynecological ultrasound;breast ultrasound;Cervical Vascular Ultrasound;thyroid ultrasound;bone density;

Countries

China

Contacts

Public ContactLin Yang

the Affiliated Hospital of Guizhou Medical University

Yanglinlin@163.com+86 139 8488 5851

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026