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1.
Medicine (Baltimore) ; 99(1): e18653, 2020 Jan.
Article in English | MEDLINE | ID: mdl-31895829

ABSTRACT

BACKGROUND: To compare the efficacy of serotonin-norepinephrine reuptake inhibitors (SNRIs) treatment for chemotherapy-induced peripheral neuropathy (CIPN) METHODS:: Two authors independently searched MEDLINE, Embase, Cochran Library, and Web of Science to identify and review articles published from January 1998 until December 2018 according to selection criteria. Outcomes were expressed as mean difference, the pooled odds ratio, or relative risk in a meta-analysis model. RESULTS: A total of 10 studies were included in this meta-analysis: 6 randomized-controlled studies and 4 observational studies. Meta-analysis showed that CIPN was improved after treatment with SNRI (standardized mean difference = 2.20; 95% confidence interval, 0.90-3.49; I = 93% in 3 randomized controlled studies). Somnolence and insomnia occurred in <15% of patients. Incidence of somnolence was lower than with pregabalin treatment, and insomnia was comparable to that in expectant management or pregabalin treatment. Incidence of nausea and vomiting was higher than in expectant management, but no significant difference was found when compared to expectant management. CONCLUSION: From the several available studies suitable for indirect comparison, SNRI shows excellent efficacy and tolerability to CIPN. SNRI could provide an important treatment option for CIPN.


Subject(s)
Antineoplastic Agents/adverse effects , Peripheral Nervous System Diseases/drug therapy , Serotonin and Noradrenaline Reuptake Inhibitors/therapeutic use , Humans , Peripheral Nervous System Diseases/chemically induced
2.
Arch Gynecol Obstet ; 300(3): 737-750, 2019 09.
Article in English | MEDLINE | ID: mdl-31172307

ABSTRACT

OBJECTIVE: To evaluate the effect of pretreatment with combined oral contraceptives (COC) on outcomes in women with polycystic ovary syndrome (PCOS) who underwent assisted reproductive technology for subfertility. METHODS: Two authors independently searched MEDLINE, EMBASE, and the Cochran Library to identify and review articles published from October 1995 until December 2018 according to selection criteria. Outcomes are expressed as mean difference and odds ratio (OR) in a meta-analysis model. RESULTS: A total of seven studies were included in this meta-analysis: one randomized controlled study and two prospective and four retrospective cohort studies. Meta-analysis showed that the COC pretreatment did not affect rate of clinical pregnancy (OR = 0.93, 95% confidence interval CI 0.65-1.34, I2 = 76%) or ovarian hyperstimulation syndrome (OR = 0.90, 95% CI 0.57-1.44, I2 = 0%). However, the rate of miscarriage in the COC group was significantly higher (OR = 1.33, 95% CI 1.02-1.72, I2 = 9%) and the rate of cumulative live birth was significantly lower compared with the control group (OR = 0.72, 95% CI 0.54-0.98, I2 = 55%). Subgroup analysis showed higher rates of miscarriage and lower rates of cumulative live birth in studies with a gonadotropin-releasing hormone (GnRH) antagonist protocol (OR = 1.69, 95% CI 1.17-2.44, I2 = 0% and OR = 0.38, 95% CI 0.29-0.50, respectively). CONCLUSION: Pretreatment with COC in women with PCOS before assisted reproductive technology may have an adverse effect on clinical outcomes, especially with a GnRH antagonist protocol.


Subject(s)
Contraceptives, Oral, Combined/therapeutic use , Infertility/therapy , Ovarian Hyperstimulation Syndrome , Polycystic Ovary Syndrome/drug therapy , Reproductive Techniques, Assisted , Abortion, Spontaneous/epidemiology , Contraceptives, Oral, Combined/administration & dosage , Female , Humans , Live Birth , Ovulation Induction/methods , Pregnancy , Pregnancy Outcome/epidemiology , Pregnancy Rate , Pregnancy, Multiple
3.
Eur J Obstet Gynecol Reprod Biol ; 231: 85-92, 2018 Dec.
Article in English | MEDLINE | ID: mdl-30336309

ABSTRACT

OBJECTIVE: To compare the efficacy of levonorgestrel releasing intrauterine system (LNG-IUS) with other treatments as a postoperative maintenance therapy for endometriosis in terms of pain reduction, recurrence prevention, side effects and patients' satisfaction. STUDY DESIGN: We searched MEDLINE, EMBASE, and the Cochrane Library from January 1986 until February 2018. Two evaluators independently extracted and reviewed prospective and retrospective articles based on pre-determined selection criteria. Outcomes were expressed as mean difference (MD), risk ratios (RR) or odds ratios (OR) in a meta-analysis model, using Revman software. RESULTS: Among the 962 studies, 7 studies were selected: 7 studies included 4 randomized controlled trials with 212 patients, 1 prospective cohort study with 88 patients, and 2 retrospective studies with 191 patients. A meta-analysis showed that LNG-IUS was significantly effective in reducing pain after surgery (MD = 12.97, 95% confidence interval (CI): 5.55-20.39), with a comparable effect to gonadotropin-releasing hormone analogues (MD = -0.16, 95% CI: -2.02 to 1.70). LNG-IUS was also effective in decreasing the recurrence rate (RR = 0.40, 95% CI: 0.26-0.64), with an effect comparable to OC (OR = 1.00, 95% CI: 0.25-4.02) and danazol (RR = 0.30, 95% CI: 0.03-2.81). Furthermore, patients' satisfaction with LNG-IUS was significantly higher than that with OC (OR = 8.60, 95% CI: 1.03-71.86). However, vaginal bleeding was significantly higher in the LNG-IUS group than in the gonadotropin-releasing hormone analogue group (RR = 27.0, 95% CI: 1.71-425.36). CONCLUSION: Our meta-analysis found a positive effect of LNG-IUS as a postoperative maintenance therapy for endometriosis on pain relief, prevention of dysmenorrhea recurrence, and patients' satisfaction.


Subject(s)
Endometriosis/drug therapy , Endometriosis/surgery , Intrauterine Devices, Medicated , Levonorgestrel/administration & dosage , Postoperative Care , Dysmenorrhea/prevention & control , Endometriosis/therapy , Female , Humans , MEDLINE , Pain Management , Patient Satisfaction , Prospective Studies , Randomized Controlled Trials as Topic , Recurrence , Retrospective Studies , Secondary Prevention , Uterine Hemorrhage
4.
Neuroepidemiology ; 44(1): 51-63, 2015.
Article in English | MEDLINE | ID: mdl-25721193

ABSTRACT

BACKGROUND: Observational epidemiological studies such as cross-sectional, case-control, and cohort studies have reported inconsistent findings regarding the association between caffeine intake from coffee or tea and the risk of cognitive disorders such as dementia, Alzheimer's disease, cognitive impairment, and cognitive decline. METHODS: We searched PubMed and EMBASE in September 2014. Three evaluators independently extracted and reviewed articles, based on predetermined selection criteria. RESULTS: Out of 293 articles identified through the search and bibliographies of relevant articles, 20 epidemiological studies from 19 articles, which involved 31,479 participants (8,398 in six cross-sectional studies, 4,601 in five case-control studies, and 19,918 in nine cohort studies), were included in the final analysis. The pooled odds ratio (OR) or relative risk (RR) of caffeine intake from coffee or tea for cognitive disorders (dementia, Alzheimer's disease, cognitive impairment, and cognitive decline) was 0.82 (95% confidence interval [CI], 0.67-1.01, I² = 63.2%) in a random-effects meta-analysis. In the subgroup meta-analysis by caffeine sources, the summary OR or RR of coffee intake was 0.83 (95% CI, 0.70-0.98; I² = 44.8%). However, in the subgroup meta-analysis by study design, the summary estimates (RR or OR) of coffee intake for cognitive disorders were 0.70 (95% CI, 0.50-0.98; I² = 42.0%) for cross-sectional studies, 0.82 (95% CI, 0.55-1.24; I² = 33.4%) for case-control studies, and 0.90 (95% CI, 0.59-1.36; I² = 60.0%) for cohort studies. CONCLUSIONS: This meta-analysis found that caffeine intake from coffee or tea was not associated with the risk of cognitive disorders.


Subject(s)
Alzheimer Disease/epidemiology , Caffeine/adverse effects , Coffee/adverse effects , Cognition Disorders/epidemiology , Dementia/epidemiology , Tea/adverse effects , Alzheimer Disease/etiology , Case-Control Studies , Cognition Disorders/etiology , Cohort Studies , Dementia/etiology , Humans , Risk
5.
Arterioscler Thromb Vasc Biol ; 34(8): 1763-9, 2014 Aug.
Article in English | MEDLINE | ID: mdl-24925973

ABSTRACT

OBJECTIVE: The current data regarding the association between calcium and phosphorus and cardiovascular disease are lacking. The aim of this study was to explore whether dietary calcium and phosphorus intake and their serum levels are associated with the prevalence of coronary artery calcification (CAC) using cardiac computed tomography in asymptomatic participants without a history of chronic kidney disease or cardiovascular disease. APPROACH AND RESULTS: A cross-sectional study was performed in 23 652 Korean participants (40.8±7.3 years, male 83.5%) without chronic kidney disease (estimated glomerular filtration rate≥60 mL/min per 1.73 m(2)) or clinically overt cardiovascular disease, who underwent cardiac computed tomographic estimation of CAC scores as part of a general health checkup in addition to completing a self-administered food frequency questionnaire. We assessed the relationship of dietary calcium and phosphorus intake and serum levels with CAC scores using both multivariate-adjusted Tobit models and multinomial logistic regression models. Neither dietary calcium nor phosphorus intake was consistently associated with CAC scores. However, the serum calcium, phosphorus, and calcium-phosphorus product levels were significantly associated with the CAC score ratios. In multivariable-adjusted models, the CAC score ratios (95% confidence intervals) comparing the highest quartiles of serum calcium, phosphorus, and calcium-phosphorus product levels to the lowest quartiles were 1.89 (1.36-2.64), 3.33 (2.55-4.35), and 3.98 (3.00-5.28), respectively (P for trend <0.001). CONCLUSIONS: Elevated serum levels of calcium, phosphorus, and calcium-phosphorus product, but not dietary consumption, are associated with increased CAC scores. Our findings should be explored in further research.


Subject(s)
Calcium, Dietary/blood , Coronary Artery Disease/blood , Phosphorus, Dietary/blood , Vascular Calcification/blood , Adult , Asymptomatic Diseases , Biomarkers/blood , Coronary Angiography/methods , Coronary Artery Disease/diagnostic imaging , Coronary Artery Disease/epidemiology , Cross-Sectional Studies , Female , Humans , Linear Models , Male , Middle Aged , Multidetector Computed Tomography , Multivariate Analysis , Nutrition Assessment , Predictive Value of Tests , Prevalence , Republic of Korea/epidemiology , Risk Factors , Surveys and Questionnaires , Up-Regulation , Vascular Calcification/diagnostic imaging , Vascular Calcification/epidemiology
6.
Obesity (Silver Spring) ; 22(2): 518-25, 2014 Feb.
Article in English | MEDLINE | ID: mdl-23512944

ABSTRACT

OBJECTIVE: This study aimed to examine the association between obesity and the risk of colorectal adenomatous polyps. DESIGN AND METHODS: The design of this study is a cross-sectional study. A total of 1,574 participants (818 males and 756 females), who had undergone colonoscopy for health examinations at the National Cancer Center hospital in South Korea from February to September 2009, were included in the analysis. RESULTS: The prevalence of colorectal adenomatous polyps was 39.5% in males and 22.6% in females. In multiple logistic regression analysis, obesity (odds ratio [OR] = 1.69, 95% CI = 1.16-2.48) and abdominal obesity (OR = 1.59, 95% CI = 1.13-2.23) were significantly associated with an increased risk of colorectal adenomatous polyps in males, but not in females. In the subgroup analyses by age, obesity (OR = 2.27, 95% CI = 1.32-3.89), and abdominal obesity (OR = 1.76, 95% CI = 1.12-2.76) significantly increased a risk of colorectal adenomatous polyps in males aged <50 years, but not in males aged ≥50 years. However, interaction terms were not significant between obesity and gender (P = 0.397) and between obesity and age (P = 0.531) in the overall analyses. CONCLUSION: Our findings should be explored in further research.


Subject(s)
Adenomatous Polyps/complications , Colorectal Neoplasms/complications , Obesity/complications , Adenomatous Polyps/diagnosis , Adenomatous Polyps/epidemiology , Adult , Age Factors , Aged , Aged, 80 and over , Body Mass Index , Colonoscopy , Colorectal Neoplasms/diagnosis , Colorectal Neoplasms/epidemiology , Cross-Sectional Studies , Early Detection of Cancer , Female , Humans , Male , Middle Aged , Obesity, Abdominal/complications , Prevalence , Republic of Korea/epidemiology , Risk Factors , Sex Factors , Waist Circumference , Young Adult
7.
Support Care Cancer ; 21(11): 3071-7, 2013 Nov.
Article in English | MEDLINE | ID: mdl-23828393

ABSTRACT

PURPOSE: The purpose of this study was to evaluate the prognostic role of interleukin-6 (IL-6) and tumour necrosis factor-alpha (TNF-α) in the survival of patients with advanced cancer. METHODS: In this prospective cohort study between three hospice and palliative care centres in South Korea, we followed 98 advanced cancer patients until death or the end of the study. Approximately 60 % of the patients had poor functional status (Eastern Cooperative Oncology Group score ≥3). We investigated the symptoms of cancer cachexia anorexia syndrome, possible cytokine-related confounders such as infection and medication records. Influence from clinical variables was adjusted using the Cox proportional hazard model. RESULTS: The median survival time was 27 days. On multivariate analysis, elevated IL-6 (hazard ratio, 2.139; p = 0.003) was found to be an independent significant prognostic factor. TNF-α was not a significant factor. Poor performance status and male gender were also independently related to shortened survival. CONCLUSIONS: IL-6 level can be a useful indicator of survival time of patients with advanced cancer at the very end of life. In contrast, the prognostic role of TNF-α requires further study.


Subject(s)
Interleukin-6/blood , Neoplasms/metabolism , Neoplasms/mortality , Tumor Necrosis Factor-alpha/blood , Aged , Anorexia/metabolism , Anorexia/mortality , Cachexia/metabolism , Cachexia/mortality , Female , Hospices , Humans , Kaplan-Meier Estimate , Male , Middle Aged , Palliative Care , Predictive Value of Tests , Prognosis , Proportional Hazards Models , Prospective Studies , Republic of Korea/epidemiology , Risk Factors
8.
Arch Intern Med ; 172(9): 686-94, 2012 May 14.
Article in English | MEDLINE | ID: mdl-22493407

ABSTRACT

BACKGROUND: Although previous randomized, double-blind, placebo-controlled trials reported the efficacy of omega-3 fatty acid supplements in the secondary prevention of cardiovascular disease (CVD), the evidence remains inconclusive. Using a meta-analysis, we investigated the efficacy of eicosapentaenoic acid and docosahexaenoic acid in the secondary prevention of CVD. METHODS: We searched PubMed, EMBASE, and the Cochrane Library in April 2011. Two of us independently reviewed and selected eligible randomized controlled trials. RESULTS: Of 1007 articles retrieved, 14 randomized, double-blind, placebo-controlled trials (involving 20 485 patients with a history of CVD) were included in the final analyses. Supplementation with omega-3 fatty acids did not reduce the risk of overall cardiovascular events (relative risk, 0.99; 95% CI, 0.89-1.09), all-cause mortality, sudden cardiac death, myocardial infarction, congestive heart failure, or transient ischemic attack and stroke. There was a small reduction in cardiovascular death (relative risk, 0.91; 95% CI, 0.84-0.99), which disappeared when we excluded a study with major methodological problems. Furthermore, no significant preventive effect was observed in subgroup analyses by the following: country location, inland or coastal geographic area, history of CVD, concomitant medication use, type of placebo material in the trial, methodological quality of the trial, duration of treatment, dosage of eicosapentaenoic acid or docosahexaenoic acid, or use of fish oil supplementation only as treatment. CONCLUSION: Our meta-analysis showed insufficient evidence of a secondary preventive effect of omega-3 fatty acid supplements against overall cardiovascular events among patients with a history of cardiovascular disease.


Subject(s)
Cardiovascular Diseases/prevention & control , Dietary Supplements , Fatty Acids, Omega-3/therapeutic use , Secondary Prevention , Cause of Death , Docosahexaenoic Acids/therapeutic use , Double-Blind Method , Eicosapentaenoic Acid/therapeutic use , Female , Humans , Male , Randomized Controlled Trials as Topic , Stroke/prevention & control , Treatment Outcome
9.
Palliat Med ; 26(3): 275-82, 2012 Apr.
Article in English | MEDLINE | ID: mdl-21807751

ABSTRACT

Although many cancer patients receiving palliative care experience distressing levels of fatigue, no well-designed studies have investigated contributing factors in Korean patients. We conducted a cross-sectional study using the Brief Fatigue Inventory-K (BFI-K) to measure fatigue while assessing a variety of possible correlates. Ninety patients with incurable cancer in the terminal stage (median survival: 27 days) participated in a structured interview and questionnaire related to their medical conditions and underwent blood sampling for laboratory data and cytokines, including interleukin (IL)-6 and tumor necrosis factor (TNF)-α. Body mass index, dyspnea, the Eastern Cooperative Oncology Group performance status, and levels of albumin, blood urea nitrogen (BUN), total bilirubin, and C-reactive protein were significantly associated with fatigue. However, levels of the two proinflammatory cytokines, IL-6 and TNF-α, were not significantly correlated with the BFI-K score. In stepwise multiple linear regression, fatigue was related to elevated BUN (ß = 0.376, p = 0.002), severe pain intensity (ß = 0.349, p = 0.004), and impaired performance status (ß = 0.268, p = 0.027), but not related to levels of inflammatory cytokines. In conclusion, the diagnostic work-up and therapeutic plan for patients with cancer-related fatigue should include an evaluation of laboratory parameters, pain severity, and physical performance.


Subject(s)
Fatigue/blood , Interleukin-6/blood , Neoplasms/complications , Pain/complications , Terminally Ill , Tumor Necrosis Factor-alpha/blood , Aged , Blood Urea Nitrogen , Cross-Sectional Studies , Fatigue/complications , Fatigue/physiopathology , Female , Humans , Interviews as Topic , Male , Middle Aged , Neoplasms/blood , Palliative Care , Surveys and Questionnaires
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