Meta AnalysisID 7165

激素避孕与骨代谢

CRD42023460827

Primary Aim What is the effect in terms of changes in OC levels in healthy women of childbearing age when comparing controls and various combinations of estrogen-progestogen therapy, including those preparations with nat

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Meta Analysis Id
7165
Evidence Id
15723
Core Evidence Id
15723
Source Meta Analysis Id
7148
Herb2 Meta Analysis Id
HBMA007148
Crd Id
CRD42023460827
Title
Hormonal contraception and bone metabolism
Review Question
Primary Aim What is the effect in terms of changes in OC levels in healthy women of childbearing age when comparing controls and various combinations of estrogen-progestogen therapy, including those preparations with natural estrogens? Secondary Aims 1) What is the effect in terms of CTX, P1NP, NTX, PYD, DPD, calcium, ALP, sclerostin, and TRAcP 5b levels in healthy women of childbearing age, when comparing controls and various combinations of estrogen-progestogen therapy, including those with natural estrogens? 2) What is the effect in terms of changes in bone markers metabolism in women of childbearing age with specific conditions (e.g., oligomenorrhea, etc.) when comparing controls and various combinations of estrogen-progestogen therapy, including those preparations with natural estrogens? 3) What estrogen-progestogen therapy-related factors influence bone markers in patients of childbearing age when comparing controls and various combinations of estrogen-progestogen therapy, including those preparations with natural estrogens?
Study Type Included
RCT or prospective studies
Condition Being Studied
Oral contraceptives are used by many women around the world. Combined oral contraceptives (COCs) can be used both for contraceptive purposes and therapeutic purposes in cases of PCOS and abnormal bleeding [1]. The close relationship between estrogen and bone metabolism is known. This relationship is of greatest concern in adolescent girls [2]. Some data suggest that COCs may inhibit the development of peak bone mass, particularly if started during adolescence [3]. The onset of COC in the early years after menarche would appear to be a major determinant of impaired bone mass acquisition. It is unclear whether the impact on bone depends on the type of estrogen used and its dose [3]. On the other hand, it is known that the decrease in endogenous levels of estradiol that occurs in menopause is a factor that contributes to the development of osteoporosis. Estradiol, in fact, slows down the rate of bone remodeling and protects against bone loss [4]. Bone loss emerges from an imbalance between bone-resorbing osteoclasts and bone-forming osteoblasts. The etiology of this imbalance depends on the risk factors present in the patient. Bone remodeling can be assessed by bone turnover markers [5, 6].
Participant
Women of childbearing age
Animal
Human Disease Modelled
Intervention
Estrogen-progestogen therapy
Comparator Control
Pre-post treatment modification Other estrogen-progestogen therapy
Main Outcome
Osteocalcin (OC) Measures of effect Assessment of osteocalcin (OC) levels before and after treatment or in controls
Outcome Measure
Additional Outcome
CTX, P1NP, NTX, PYD, DPD, calcium, ALP, sclerostin, and TRAcP 5b levels. In the included studies also bone mass assessment will be analyzed. Measures of effect Assessment of CTX, P1NP, NTX, PYD, DPD, calcium, ALP, sclerostin, and TRAcP 5b levels and bone mass before and after treatment or in controls.
Study Method
Systematic review
Keyword
Calcium, Dietary; Estrogens; Female; Hormonal Contraception; Humans; Oligomenorrhea; Progestins; Tartrate-Resistant Acid Phosphatase
Contact
Ambrogio P Londero [email protected]
Organisational Affiliation
University of Genoa www.unige.it
Funding Source
None to declare Grant number(s) State the funder, grant or award number and the date of award None to declare
Other Selection Criteria
Final Publication
Same Topic Review
None found
Published Protocol
Review Type
Language
English
Country
Italy
Review Stage
Review Ongoing
First Submission Date
2023-09-05
Registration Date
2023-09-16
Anticipated Start Date
2023-09-11
Anticipated Completion Date
2024-03-31
Title Cn
激素避孕与骨代谢
Title En
Hormonal contraception and bone metabolism
Bilingual Status
complete