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1.
J Clin Med ; 12(5)2023 Feb 24.
Article in English | MEDLINE | ID: mdl-36902618

ABSTRACT

The aim of the report was to evaluate whether in utero exposure to paracetamol is associated with risk towards developing respiratory disorders such as asthma and wheeze after birth. MEDLINE (PubMed), EMBASE and Cochrane Library databases were searched for articles published in English to December 2021. The study involved 330,550 women. We then calculated the summary risk estimates and 95% CIs and plotted forest plots using random effect models (DerSimonian-Laird method) and fixed effect models. We also performed a systematic review of the chosen articles and a meta-analysis of studies based on the guidelines outlined in the PRISMA statement. Accordingly, maternal exposure to paracetamol during pregnancy was associated with a significant increased risk of asthma: crude OR = 1.34, 95% CI: 1.22 to 1.48, p < 0.001; and significant increased risk of wheeze: crude OR = 1.31, 95% CI: 1.12 to 1.54, p < 0.002. Results of our study confirmed that maternal paracetamol use in pregnancy is associated with an enhanced risk of asthma and wheezing in their children. We believe paracetamol should be used with caution by pregnant women, and at the lowest effective dose, and for the shortest duration. Long-term use or the use of high doses should be limited to the indications recommended by a physician and with the mother-to-be under constant supervision.

2.
Cancers (Basel) ; 14(19)2022 09 29.
Article in English | MEDLINE | ID: mdl-36230696

ABSTRACT

Oral contraceptive use is one of the major modifiable risk factors for breast cancer. To investigate the effect of oral contraceptive taking on breast cancer risk by BRCA 1 and BRCA 2 mutation status, we conducted a systematic review and meta-analysis of case-controlled studies. Therefore, English language articles were retrieved by searching MEDLINE (PubMed), EMBASE and the Cochrane Library up to August 2021. Data were pooled from none case-control studies, comprising a total of 33,162 subjects, including 23,453 who had never used oral contraceptives. Overall meta-analysis indicated a statistically insignificant risk reduction: OR = 0.86, 95% CI: 0.70 to 1.06, p = 0.1594. However, increased breast cancer risk was associated with age at first use of OCs ≥20 years: OR = 1.21, 95% CI:1.07 to 1.36, p = 0.002. Multivariable meta-regression with covariates of age of first OC use (ß = 0.21, 95% CI: -0.25 to 0.67, p = 0.3767), duration of OC use (ß = -0.08, 95% CI; -0.51 to 0.34, p = 0.7093), and time since last OC use (ß = 0.32, 95% CI: -0.22 to 0.85, p = 0.2461) did not have a significant effect on the breast cancer risk. This meta-analysis suggests a diverse effect of oral contraceptive use against breast cancer in BRCA carrier mutation. The association between OC use and breast and ovarian cancers needs more investigation.

3.
J Clin Med ; 11(16)2022 Aug 10.
Article in English | MEDLINE | ID: mdl-36012916

ABSTRACT

The aim of the report was to determine the effects of soy isoflavones on lumbar spine, femoral neck, and total hip bone mineral density (BMD) in menopausal women. MEDLINE (PubMed), EMBASE, and Cochrane Library databases were searched for articles published in English during 1995-2019. Studies were identified and reviewed for inclusion and exclusion eligibility. Weighted mean differences (WMD) were calculated for each study and were pooled by using the random effects model. Eighteen randomized controlled trials were selected for meta-analysis. Different types of soy phytoestrogens, i.e., genistein extracts, soy isoflavones extracts, soy protein isolate, and foods containing diverse amounts of isoflavones were used in the studies. The analysis showed that daily intake of 106 (range, 40-300) mg of isoflavones for 6-24 months moderately but statistically significantly positively affects BMD, compared with controls: lumbar spine WMD = 1.63 (95% CI: 0.51 to 2.75)%, p = 0004; femoral neck WMD = 1.87 (95% CI: 0.14 to 3.60)%, p = 0.034; and total hip WMD = 0.39 (95% CI: 0.08 to 0.69)%, p = 0.013. Subgroups analyses indicated that the varying effects of isoflavones on BMD across the trials might be associated with intervention duration, racial diversity (Caucasian, Asian), time after menopause, form of supplements (especially genistein), and dose of isoflavones. Our review and meta-analysis suggest that soy isoflavones are effective in slowing down bone loss after menopause.

4.
Nutrients ; 14(12)2022 Jun 14.
Article in English | MEDLINE | ID: mdl-35745197

ABSTRACT

The aim of this report was to determine the impact of flaxseed, soy and red clover, and their bioactive substances on the lipid profile in postmenopausal women in cardiovascular diseases prevention. We used the following databases: MEDLINE (PubMed), EMBASE and the Cochrane Library. Meta-analysis indicates that the intake of flaxseed by postmenopausal women is associated with a statistically significant reduction in total cholesterol (TC) levels (weighted-mean difference (WMD) = -0.26; 95% confidence interval (95% CI): -0.38 to -0.13; p = 0.0001), low-density lipoprotein cholesterol (LDL-C) levels (WMD = -0.19; 95% CI: -0.30 to -0.08; p = 0.0006), and high-density lipoprotein cholesterol (HDL-C) levels (WMD = -0.06; 95% CI: -0.11 to -0.01; p = 0.0150). The effect of soy protein on the lipid profile showed a significant decrease in TC levels: WMD = -0.15; 95% CI: -0.25-0.05; p = 0.0048, LDL-C levels: WMD = -0.15; 95% CI: -0.25-0.05; p = 0.0067, as well as a significant increase in HDL-C levels: WMD = 0.05; 95% CI: 0.02-0.08; p = 0.0034. Changes in the lipid profile showed a significant reduction in TC levels after the use of red clover (WMD = -0.11; 95% CI: -0.18--0.04; p = 0.0017) and a significant increase in HDL-C levels (WMD = 0.04; 95% CI: 0.01 to 0.07; p = 0.0165). This meta-analysis provides evidence that consuming flaxseed, soy and red clover can have a beneficial effect on lipids in postmenopausal women and suggest a favorable effect in preventing cardiovascular diseases.


Subject(s)
Cardiovascular Diseases , Flax , Trifolium , Cardiovascular Diseases/prevention & control , Cholesterol, LDL , Female , Humans , Phytoestrogens/pharmacology , Postmenopause , Glycine max
5.
Cancers (Basel) ; 14(3)2022 Jan 23.
Article in English | MEDLINE | ID: mdl-35158842

ABSTRACT

We conducted a systematic review and meta-analysis to investigate the effect of oral contraceptives (OCs) on risk of breast cancer (BrCa) by status of estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER2). We searched the MEDLINE (PubMed), Embase and the Cochrane Library database and bibliographies of pertinent articles published up to 2020. Therein, we identified nineteen eligible case-control studies which provided data by breast cancer subtypes: ER-positive (ER+), ER-negative (ER-), HER2-positive (HER2+) and Triplet-negative (TN). Summary risk estimates (pooled OR [pOR]) and 95% confidence intervals (CIs) were calculated using fixed/random effects models. The summary meta-analysis showed that over-use of OCs led to significant increased risk of TNBrCa (OR = 1.37, 95% CI; 1.13 to 1.67, p = 0.002), as well as of ER-BrCa (OR = 1.20, 95% CI: 1.03 to 1.40, p = 0.019). There was also a significant reduction in the risk of ER+BrCa (OR = O.92, 95% CI: 0.86 to 0.99, p = 0.026,) and a slight reduction in the risk of HER2+BrCa (OR = 0.95, 95% CI; 0.79 to 1.14, p = 0.561) after taking OCs. Meta-analysis indicated that OC use has different impacts on risk of breast cancer subtypes defined by receptor status. The identified differences between individual subtypes of breast cancer may reflect different mechanisms of carcinogenesis.

6.
Cancers (Basel) ; 13(22)2021 Nov 12.
Article in English | MEDLINE | ID: mdl-34830807

ABSTRACT

To perform a meta-analysis of case-control studies that addressed the association between oral contraceptive pills (OC) use and breast cancer (BrCa), PubMED (MEDLINE), Embase, and the Cochrane Library were searched to identify case-control studies of OC and BrCa published between 2009 and 2020. We used the DerSimonian-Laird method to compute pooled odds ratios (ORs) and confidence intervals (CIs), and the Mantel-Haenszel test to assess the association between OC use and cancer. Forty-two studies were identified that met the inclusion criteria and we included a total of 110,580 women (30,778 into the BrCa group and 79,802 into the control group, of which 15,722 and 38,334 were using OC, respectively). The conducted meta-analysis showed that the use of OC was associated with a significantly increased risk of BrCa in general, OR = 1.15, 95% CI: 1.01 to 1.31, p = 0.0358. Regarding other risk factors for BrCa, we found that increased risk was associated significantly with early menarche, nulliparous, non-breastfeeding, older age at first parity, postmenopause, obesity, smoking, and family history of BrCa. Despite our conclusion that birth control pills increase the cancer risk being supported by extensive previous studies and meta-analyzes, further confirmation is required.

7.
Nutrients ; 13(8)2021 Jul 24.
Article in English | MEDLINE | ID: mdl-34444691

ABSTRACT

The aim of the report was to evaluate the impact of soy protein containing isoflavones and soy isoflavones extract on lipid profile in postmenopausal women, as compared with placebo or protein of milk, casein or isolated soy protein with or without trace isoflavone content. We used the following databases: MEDLINE (PubMed), EMBASE and the Cochrane Library. Quantitative data synthesis was performed by applying a random-effects model. Subgroup analysis and meta-regression were performed to assess the modifiers of treatment response. In total, in the analysis studies, 2305 postmenopausal women took part. Changes in the lipid profile showed statistically significant decreases of total cholesterol by -0.12 (95% CI: -0.21, -0.03) mmol/L, -4.64 (95% CI: -8.12, -1.16) mg/dL, p = 0.01 and increased HDL-cholesterol by 0.03 (95% CI: 0.00, 0.06) mmol/L, 1.15 (95% CI: 0.00, 1.93) mg/dL, p = 0.05, as well as in LDL-cholesterol -0.05 (95% CI: -0.11, 0.01) mmol/L, -1.93 (95% CI: -4.25, 0.39) mg/dL, p = 0.08 and triacylglycerols -0.07 (95% CI: -0.14, 0.00) mmol/L, -6.123 (95% CI: -12.25, 0.00) mg/dL, p = 0.06. Our results suggests that soy and its isoflavones can be effective in correction changes in lipid metabolism in postmenopausal women and may favorably influence in preventing cardiovascular events.


Subject(s)
Cardiovascular Diseases/prevention & control , Lipids/blood , Plant Extracts/administration & dosage , Postmenopause/blood , Soybean Proteins/administration & dosage , Cholesterol, HDL/blood , Cholesterol, LDL/blood , Female , Humans , Isoflavones/administration & dosage , Lipid Metabolism/drug effects , Middle Aged , Randomized Controlled Trials as Topic , Triglycerides/blood
8.
Nutrients ; 13(6)2021 May 31.
Article in English | MEDLINE | ID: mdl-34072748

ABSTRACT

The aim of the report was to investigate the impact of soy protein and isoflavones on glucose homeostasis and lipid profile in type 2 diabetes. The studies used in this report were identified by searching through the MEDLINE and EMBASE databases (up to 2020). Meta-regression and subgroup analyses were performed to explore the influence of covariates on net glycemic control and lipid changes. Weighted mean differences and 95% confidence intervals (CI) were calculated by using random-effect models. Changes in the lipid profile showed statistically significant decreases in total cholesterol and LDL-C concentrations: ‒0.21 mmol/L; 95% CI, ‒0.33 to ‒0.09; p = 0.0008 and ‒0.20 mmol/L; 95% CI, ‒0.28 to ‒0.12; p < 0.0001, respectively, as well as in HDL-C (-0.02 mmol/L; 95% CI, -0.05 to 0.01; p = 0.2008 and triacylglycerols (-0.19 mmol/L; 95% CI, -0.48 to 0.09; p = 0.1884). At the same time, a meta-analysis of the included studies revealed statistically insignificant reduction in fasting glucose, insulin, HbA1c, and HOMA-IR (changes in glucose metabolism) after consumption of soy isoflavones. The observed ability of both extracted isoflavone and soy protein with isoflavones to modulate the lipid profile suggests benefits in preventing cardiovascular events in diabetic subjects. Further multicenter studies based on larger and longer duration studies are necessary to determine their beneficial effect on glucose and lipid metabolism.


Subject(s)
Diabetes Mellitus, Type 2 , Glycemic Control , Isoflavones , Lipids/blood , Soybean Proteins , Aged , Blood Glucose/drug effects , Blood Glucose/physiology , Diabetes Mellitus, Type 2/blood , Diabetes Mellitus, Type 2/physiopathology , Diabetes Mellitus, Type 2/therapy , Female , Glycated Hemoglobin/analysis , Humans , Lipid Metabolism/drug effects , Lipid Metabolism/physiology , Male , Middle Aged
9.
Article in English | MEDLINE | ID: mdl-34067865

ABSTRACT

This systematic review and meta-analysis of randomized controlled trials was performed to more completely assess potential changes in bone turnover marker levels in postmenopausal women during the intake of soy isoflavones. PubMed (Medline) and EMBASE were searched for relevant studies, and their quality was evaluated according to Cochrane criteria. The levels of markers were evaluated in a total of 1114 women who ingested mean daily doses of 98.2 mg (30.9 to 300) of soy isoflavones for 3 to 24 months, in comparison to those of 1081 subjects who used a placebo. Ten, eighteen, eight, and fourteen comparison studies were finally selected for an estimation of the effects on osteocalcin (OC), bone alkaline phosphatase (BAP), pyridinoline (PYD), and deoxypyridinoline (DPD), respectively. A summary of the results of intervention was as follows: 4.16%, 95% CI: -7.72-16.04, p = 0.49 for OC; 5.50%, 95% CI: -3.81-14.82, p = 0.25 for BAP; -12.09%, 95% CI: -25.37-1.20, p = 0.07 for PYD; and -7.48%, 95% CI: -15.37-0.41, p = 0.06 for DPD. The meta-analysis of the included studies revealed some statistically insignificant observations that soy isoflavones intake is associated with a trend in increased levels of OC and BAP, as well as a trend in reduced levels of PYD and DPD. Soy isoflavones may have a beneficial effect on bone formation markers, but this requires extensive multi-center research.


Subject(s)
Isoflavones , Biomarkers , Bone Density , Female , Humans , Postmenopause , Randomized Controlled Trials as Topic , Glycine max
10.
Article in English | MEDLINE | ID: mdl-33925599

ABSTRACT

Despite numerous studies evaluating the risk of breast cancer among oral contraception users, the effect of oral contraceptive on developing breast cancer remains inconclusive. Therefore, we conducted a systematic review of literature with meta-analysis in order to quantitative estimate this association. The bibliographic database MEDLINE and EMBASE, and reference lists of identified articles were searched, with no language restrictions, from the start of publication to August 2010. We performed a reanalysis and overall estimate of 79 case-control studies conducted between 1960-2010, including a total of 72,030 incidents, histologically confirmed cases of breast cancer and 123,650 population/hospital controls. A decrease was observed in cancer risk in OC users before age 25 years (0.91, 0.83-1.00). However, the use of OCs before the first full-term pregnancy had a significant increased risk of breast cancer (OR, 1.14, 1.01-1.28, p = 0.04), as did OC use longer than 5 years (1.09, 1.01-1.18, p = 0.02). Pooled crude odds ratios of breast cancer in ever-users of oral contraceptives was 1.01 [95% confidence interval (CI), 0.95-1.07], compared with never-users. There was no significant increase in risk among premenopausal women (1.06, 0.92-1.22), postmenopausal women (0.99, 0.89-1.10), or nulliparous women (1.02, 0.82-1.26). Oral contraceptives do not appear to increase the risk of breast cancer among users. However, OC use before a first full-term pregnancy or using them longer than 5 years can modify the development of the breast cancer.


Subject(s)
Breast Neoplasms , Contraceptives, Oral , Adult , Breast Neoplasms/chemically induced , Breast Neoplasms/epidemiology , Case-Control Studies , Contraceptives, Oral/adverse effects , Female , Humans , Odds Ratio , Pregnancy , Risk Factors
11.
Nutrients ; 13(4)2021 Apr 11.
Article in English | MEDLINE | ID: mdl-33920485

ABSTRACT

The meta-analysis presented in this article covered the efficacy of red clover isoflavones in relieving hot flushes and menopausal symptoms in perimenopausal and postmenopausal women. Studies were identified by MEDLINE (PubMed), Embase, and the Cochrane Library searches. The quality of the studies was evaluated according to Cochrane criteria. A meta-analysis of eight trials (ten comparisons) demonstrated a statistically significant reduction in the daily incidence of hot flushes in women receiving red clover compared to those receiving placebo: weighted mean difference (WMD-weighted mean difference) -1.73 hot flushes per day, 95% CI (confidence interval) -3.28 to -0.18; p = 0.0292. Due to 87.34% homogeneity, the performed analysis showed substantive difference in comparisons of postmenopausal women with ≥5 hot flushes per day, when the follow-up period was 12 weeks, with an isoflavone dose of ≥80 mg/day, and when the formulations contained a higher proportion of biochanin A. The meta-analysis of included studies assessing the effect of red clover isoflavone extract on menopausal symptoms showed a statistically moderate relationship with the reduction in the daily frequency of hot flushes. However, further well-designed studies are required to confirm the present findings and to finally determine the effects of red clover on the relief of flushing episodes.


Subject(s)
Hot Flashes/drug therapy , Isoflavones/administration & dosage , Plant Extracts/administration & dosage , Trifolium/chemistry , Female , Follow-Up Studies , Hot Flashes/physiopathology , Humans , Perimenopause/drug effects , Perimenopause/physiology , Plant Extracts/chemistry , Postmenopause/drug effects , Postmenopause/physiology , Randomized Controlled Trials as Topic , Treatment Outcome
12.
Maturitas ; 132: 7-16, 2020 Feb.
Article in English | MEDLINE | ID: mdl-31883666

ABSTRACT

AIM: The aim of this systematic review and meta-analysis was to clarify the effect of a specific standardised extract of red clover (Trifolium pratense) on the lipid profile of perimenopausal and postmenopausal women. METHODS: Medline (PubMed), EMBASE, and Cochrane Library electronic databases were searched for papers in English reporting randomized controlled trials published up to 2017. Reference lists from those papers were checked for further relevant publications. Studies were identified and reviewed for their eligibility for inclusion in this review. The changes from baseline in the levels of individual components of the lipid profiles were used to assess differences between the active treatment and placebo groups. Weighted mean differences and 95 % confidence intervals were calculated for continuous data using a random-effects model. RESULTS: Ten eligible studies (twelve comparisons) with 910 peri- and postmenopausal women were selected for systematic review. The meta-analysis showed changes in serum levels: total cholesterol, -0.29 (95 % CI: -0.53 to -0.06) mmol/L [-11.21 (95 % CI: -20.49 to -13.92) mg/dL], p = 0.0136; LDL-cholesterol, -0.13 (95 % CI: -0.35 to 0.09) mmol/L [-5.02 (95 % CI: -13.53 to 3.48) mg/dL], p = 0.2418; triglycerides, -0.15 (95 % CI: -0.32 to 0.01) mmol/L [-13.28 (95 % CI: -28.34 to 0.88) mg/dL], p = 0.0592; and HDL-cholesterol, 0.14 (95 % CI: -0.08 to 0.36) mmol/L [5.41 (95 % CI: -3.09-13.92) mg/dL], p = 0.2103. TheI2 statistic ranged from 87.95%-98.30 %, indicating significant heterogeneity. CONCLUSIONS: The results suggest that a red clover extract is efficacious in reducing the concentrations of total cholesterol; however, changes in HDL-C, LDL-C and triglycerides are not as pronounced. Potentially, this means that women takingTrifolium pratense for menopausal symptoms can derive additional benefits from the plant's specific effect that corrects abnormal cholesterol levels. Additional studies are needed to assess its effects on post-menopausal women.


Subject(s)
Isoflavones/pharmacology , Lipids/blood , Plant Extracts/pharmacology , Trifolium , Cholesterol, HDL/blood , Cholesterol, LDL/blood , Female , Humans , Perimenopause/blood , Postmenopause/blood , Triglycerides/blood
13.
Ginekol Pol ; 83(4): 270-9, 2012 Apr.
Article in Polish | MEDLINE | ID: mdl-22712259

ABSTRACT

OBJECTIVE: Despite numerous studies assessing the risk of preterm birth in obese women compared with normal weight patients, the scope of the association remains unclear. Therefore, we conducted a systematic overview and meta-analysis to summarize the available evidence from cohort studies on the relationship between maternal obesity and the risk of preterm birth. METHODS: We searched bibliographic database: MEDLINE (PubMed) and EMBASE for all relevant articles, with no language restrictions, which were published from January 1990 to September 2010, using a combination of the following search terms: maternal obesity or high body mass index (BMI) and preterm birth or pregnancy outcome. Crude odds ratios (OR) for individual outcomes were calculated for each study and were pooled by using the random-effects model. RESULTS: Twenty seven studies proved eligible under the selection criteria. The crude OR of preterm birth were 1.18 [95% confidence interval (CI) 1.07 to 1.30], 1.28 (95% CI 0.93 to 1.75) and 1.1 (95% CI 0.98 to 1.25) among obese, severely obese and morbidly obese women, respectively, compared with normal weight women. We found an elevated risk of induced preterm birth among obese (OR 1.72, 95% CI 1.45 to 2.04), severely obese (OR 1.70, 95% CI 1.32 to 2.18) and morbidly obese pregnants (OR 1.66, 95% CI 1.33 to 2.07) but a reduction in the risk of spontaneous preterm birth: OR = 0.98 (95% CI 0.80 to 1.20), OR = 0.85 (95% CI 0.55 to 7.31) and OR = 0.77 (95% CI 0.60 to 0.99), respectively. Obese women, independently of category the of obesity also are at a higher risk of very preterm delivery (- < 32 weeks). CONCLUSIONS: Maternal obesity is associated with an increased risk of medically indicated preterm birth and with a decrease in the risk of spontaneous preterm birth. It appears that slightly increased risk of preterm birth overall may be masked by the increase in the incidence of induced preterm birth.


Subject(s)
Maternal Welfare/statistics & numerical data , Obesity/epidemiology , Pregnancy Complications/epidemiology , Pregnancy Outcome/epidemiology , Premature Birth/epidemiology , Adult , Body Mass Index , Causality , Cesarean Section/statistics & numerical data , Cohort Studies , Comorbidity , Female , Humans , Pregnancy , Risk Factors , Women's Health , Young Adult
14.
Ginekol Pol ; 81(3): 215-23, 2010 Mar.
Article in Polish | MEDLINE | ID: mdl-20486545

ABSTRACT

Bariatric surgery is a safe and most effective method of achieving substantial long-term weight loss. Surgery should be considered in case of all patients with a BMI of more than 40 kg/m2 and for those with a BMI of over 35 kg/m2 with obesity-related co-morbidities, after conventional treatment failure. The most frequently used procedures in surgical treatment of obesity performed mostly laparoscopically are restrictive operations limiting energy intake by reducing gastric capacity (vertical banded gastroplasty adjustable gastric band, sleeve gastrectomy) and restrictive/ malabsorptive surgeries also inducing decreased absorption of nutrients by shortening the functional length of the small intestine (Roux-en-Y gastric bypass). Frequent complications following surgery may include hyperemesis, intragastric band migration, gastric perforation, nutritional deficiencies, anastomotic leak, bleeding, anastomotic stricture, internal hernia, wound infection. It is generally recommended for women after bariatric surgery to wait approximately at least 12 months before becoming pregnant. There exists considerable threat that rapid weight loss (relative starvation phase) may be unhealthy for a mother and a baby. Pregnancy after weight loss surgery is not only safe for the mother and the baby but may also be less risky than pregnancy in morbidly obese patients. Postoperative nutrient supplementation and close supervision before, during, and after pregnancy adjusted to individual requirements of a woman can help to prevent nutrition-related complications such as deficiencies in iron, vitamin A, vitamin B12, vitamin K, folate and calcium, and improve maternal and fetal health.


Subject(s)
Bariatric Surgery , Maternal Nutritional Physiological Phenomena , Obesity, Morbid/surgery , Pregnancy Complications/prevention & control , Pregnancy Outcome , Bariatric Surgery/adverse effects , Female , Gastroplasty/methods , Humans , Laparoscopy/methods , Maternal Welfare , Obesity/surgery , Pregnancy , Risk Factors , Surgical Wound Infection/etiology , Vomiting/etiology , Weight Loss
15.
Ginekol Pol ; 79(4): 287-96, 2008 Apr.
Article in Polish | MEDLINE | ID: mdl-18592868

ABSTRACT

The occurrence of vasomotor symptoms in women is directly related to deficiency of estrogen, which occurs as a result of natural or surgical menopause. Hot flushes may also be a major problem for patients with a history of breast cancer, as they may result directly from cancer treatment (oophorectomy, chemotherapy-induced ovarian failure or adjuvant tamoxifen citrate therapy). Despite the lack of reliable data regarding their efficacy and safety, in recent years the usage of herbs among menopausal women has increased dynamically all over the world. The following paper reviews professional literature about Black Cohosh (Actaea/Cimicifuga racemosa), either used alone or in combination with other medicinal herbs administered in management of vasomotor symptoms. Extracts of the rootstock of Black cohosh contain such potentially biologically active constituents as triterpene glycosides (actein, cimicifugoside, deoxyacetein), isoferulic acid and alkaloids (n-methylcytisine). The mechanism of its action remains unclear. Some authors suggest that Black Cohosh contains substances with selective estrogen receptor modulator (SERM) activity. Recent data has demonstrated that Black Cohosh may have an effect on dopaminergic and serotoninergic systems. Thirty-two papers formed the basis for this review. Open-label, noncomparative studies, as well as treatment-controlled, randomized, open trials, have proven that Black Cohosh significantly reduced frequency or severity of hot flashes. The results of randomized, placebo-controlled, double-blind clinical trials were contradictory. Adverse symptoms have been rare (5,4%), mild and reversible. Most of them included gastrointestinal upsets, rashes, headaches, dizziness and mastalgia. Nevertheless, single cases of serious adverse events, including acute hepatocellular damage, have been reported, but without a clear causality relationship.


Subject(s)
Cimicifuga , Hot Flashes/drug therapy , Phytotherapy/methods , Women's Health , Adult , Clinical Trials as Topic , Female , Humans , Menopause/drug effects , Middle Aged , Nonprescription Drugs/therapeutic use , Phytotherapy/adverse effects , Plant Extracts/therapeutic use , Treatment Outcome
16.
Ginekol Pol ; 76(3): 225-7, 2005 Mar.
Article in Polish | MEDLINE | ID: mdl-16018142

ABSTRACT

Sudden sensorineural hearing loss is defined as sudden, idiopathic, usually unilateral deafness developed at most within 72 hours in previously healthy person. This paper presents very rarely occurring case of sudden sensorineural hearing loss in 23-year-old healthy nulliparous women during an uncomplicated pregnancy. The possibility of therapy of that sudden deafness in pregnant women is restricted by reason of unknown cause of disease. It has been hypothesized that hearing loss may be associated with increased activation of both blood coagulation and fibrinolysis ('hypercoagulable state') which occurs during normal pregnancy. This state may lead to vascular occlusion in the microcirculation of the inner ear by microemboli. It's necessary to take certain predisposing factors into consideration as fluid and sodium retention, emotional instability, situation anxiety, viral and allergic changes. It's essential to conduct a more detailed diagnosis to exclude some organic disorders as otosclerosis, Meniere's disease with non-typical course, especially those which are dangerous for pregnant women's life--preeclampsia-eclampsia and hypertension.


Subject(s)
Hearing Loss, Sensorineural , Hearing Loss, Sudden , Pregnancy Complications , Adult , Female , Hearing Loss, Sensorineural/diagnosis , Hearing Loss, Sensorineural/etiology , Hearing Loss, Sudden/diagnosis , Hearing Loss, Sudden/etiology , Humans , Pregnancy , Pregnancy Complications/diagnosis , Pregnancy Complications/etiology
17.
Int J Fertil Womens Med ; 47(1): 38-45, 2002.
Article in English | MEDLINE | ID: mdl-11900274

ABSTRACT

It is generally accepted that menopausal symptoms can be controlled by HRT. As additional (putative) benefits of HRT were discovered, it was claimed that such uses were also important. Soon, trials were instituted to test these assertions, some of them quite large and projected to last a long time (> or = 5 years). The most instructive for medical practice are the observational trials and, still more, randomized, controlled trials. Unfortunately, the results of these trials for both primary and secondary prevention of CHD are not in agreement, although the observational trials are mostly more favorable to the benefits of HRT on CHD. The present review considers both kinds of trials and their effects on primary and secondary CHD prevention. It also attempts to group the studies by their results and their implications for guiding patients in choices and decisions regarding HRT.


Subject(s)
Cardiovascular Diseases/prevention & control , Hormone Replacement Therapy , Female , Humans , Postmenopause , Primary Prevention , Randomized Controlled Trials as Topic
18.
Ginekol Pol ; 73(10): 811-6, 2002 Oct.
Article in Polish | MEDLINE | ID: mdl-12619313

ABSTRACT

OBJECTIVE: The aim of the study was to determine the frequency of GDM in different parts of Poland and to assess whether 1 h--glucose plasma levels after 50 g glucose tolerance test (50 g OGTT) reflect the risk of GDM. MATERIAL AND METHODS: A total of 5778 pregnant women were screened with 50 g OGTT between 24 and 28 weeks of gestation. All subjects whose post-challenge glucose levels exceeded 140 mg/dl had 75 g OGTT performed according to WHO criteria. RESULTS: The rate of abnormal screening test results ranged from 8.0% to 20.7% for different regions of Poland, respectively. The pathological 50 g OGTT results were from 140 mg/dl to 320 mg/dl. Screening test results within 140 mg/dl to 149 mg/dl were confirmed by positive 75 g OGTT only in 2.9% subjects. All patients whose 1 h--glucose levels at 50 g OGTT were greater than 190 mg/dl had pathological 75 g OGTT results as well. CONCLUSION: The prevalence of GDM in different parts of Poland ranged from 2.0% to 3.8% (the average 3.4%).


Subject(s)
Blood Glucose/metabolism , Diabetes, Gestational/diagnosis , Diabetes, Gestational/epidemiology , Adult , Diabetes, Gestational/blood , Female , Glucose Tolerance Test , Humans , Poland/epidemiology , Pregnancy , Prenatal Diagnosis/methods , Prevalence , Sensitivity and Specificity , Time Factors
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