RELATIONSHIP BETWEEN CD4+ COUNT, SERUM INFLAMMATORY CYTOKINES AND ORAL MELANOTIC HYPERPIGMENTATION IN NEWLY DIAGNOSED HIV SEROPOSITIVE PATIENTS- A NESTED CASE CONTROL STUDY

Author(s):  
Elizabeth Oluwatoyin Abe ◽  
Akinyele Olumuyiwa Adisa ◽  
Bukola Folasade Adeyemi ◽  
Olutosin Alaba Awolude ◽  
Foluso John Owotade
2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Sang Oh Kang ◽  
Kyung Hyun Min ◽  
Hyun Jeong Kim ◽  
Tae Hyeok Kim ◽  
Woorim Kim ◽  
...  

Abstract Background In March 2020, the US Food and Drug Administration decided that the dangers related to neuropsychiatric events (NPEs) of montelukast, one of the leukotriene modifying agents (LTMAs), should be communicated through ‘boxed warning’. In case of NPEs, the prevalence has been the highest in elderly people. Because the characteristics of the elderly such as old age itself can act as risk factors. Therefore, an investigation on safety of LTMAs related to NPEs in elderly using LTMAs is needed. Method A nested case-control study using an elderly sample cohort from the Korean National Health Insurance Service database was used. The asthma cohort included asthma patients newly diagnosed between 2003 and 2013. Within the asthma cohort, the case group was defined as patients who were diagnosed with NPEs. Among patients who had never been diagnosed with NPEs, the control group was selected by matching 1:1 by propensity score. Patients who were prescribed LTMAs for 1 year prior to index date were defined as the exposure group. The logistic regression model was used to measure the effect of LTMAs on NPEs. Results We identified 141,165 patients with newly diagnosed asthma, and selected 31,992 patients per each case and control group. Exposure to LTMAs significantly increased the risk of overall NPEs about in comparison with the absence of exposure (crude odds ratio [OR] 1.58, 95% CI 1.50–1.68). After adjusting for confounding factors, the overall NPEs risk increased (adjusted OR, 1.67, 95% CI 1.58–1.78). Conclusion This study suggests that elderly asthma patients prescribed LTMAs had a higher risk of NPEs than patients who were not treated with LTMAs. Therefore, clinicians should be aware of the potential risks of LTMAs.


2010 ◽  
Vol 172 (3) ◽  
pp. 299-308 ◽  
Author(s):  
Jane A. Driver ◽  
Rachel Yung ◽  
J. Michael Gaziano ◽  
Tobias Kurth

2021 ◽  
Author(s):  
Junghee Ha ◽  
Dong Woo Choi ◽  
Kwang Joon Kim ◽  
So Yeon Cho ◽  
Hyunjeong Kim ◽  
...  

Abstract Background: Metformin reduces insulin resistance, which may be shared pathophysiology between diabetes mellitus (DM) and Alzheimer’s disease (AD). Thus, it has been hypothesized that metformin may be effective against AD; however, evidence of metformin effects on AD development remains insufficient and conflicting. We investigated Alzheimer’s disease risk in patients with newly diagnosed type 2 diabetes mellitus treated with metformin.Methods: This retrospective, observational, nested case-control study included enrolled patients with newly diagnosed type 2 diabetes mellitus in the Korean National Health Insurance Service diabetes mellitus cohort (2002–2017). Among 70,499 DM patients who were dementia-free at the time of DM diagnosis, 1,675 AD cases identified were matched to 8,375 controls by age, sex, and DM onset and duration. Association of AD with metformin use were analyzed using multivariable conditional logistic regression analyses adjusted for comorbidities and cardiometabolic risk profile. Results: Metformin use was associated with an increased adjusted odds ratio (AOR) of AD (1.50; 95% CI, 1.23–1.83). The strength of the association increased with the cumulative daily defined dose per day in metformin users. The risk was more pronounced among patients with a longer duration of DM (1.48; 95% CI, 1.14 to 1.91, for a DM duration of 5–9 years; 2.18; 95% CI, 1.41 to 3.39 for a duration greater than 10 years), while no statistical significance was found in the patients with DM duration less than 5 years (AOR 0.88; 95%CI 0.54–1.43). Furthermore, the risk of AD was significantly higher in DM patients with depression (AOR 2.05; 1.02–4.12). Conclusions: Given the huge number of patients with DM who are taking metformin worldwide, a double-blinded, prospective study is required to determine the long-term cognitive safety of metformin.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Junghee Ha ◽  
Dong-Woo Choi ◽  
Kwang Joon Kim ◽  
So Yeon Cho ◽  
Hyunjeong Kim ◽  
...  

AbstractMetformin reduces insulin resistance, which constitutes a pathophysiological connection of diabetes with Alzheimer’s disease (AD), but the evidence of metformin on AD development was still insufficient and conflicting. We investigated AD risk in patients with newly diagnosed type 2 DM treated with metformin. This retrospective, observational, nested case–control study included patients with newly diagnosed type 2 DM obtained from the Korean National Health Insurance Service DM cohort (2002–2017). Among 70,499 dementia-free DM patients, 1675 AD cases were matched to 8375 controls for age, sex, and DM onset and duration. The association between AD and metformin was analyzed by multivariable regression analyses, adjusted for comorbidities and cardiometabolic risk profile. Metformin use was associated with an increased odds of AD (adjusted odds ratio [AOR] 1.50; 95% CI 1.23–1.83). The risk of AD was higher in patients with a longer DM duration. Furthermore, AD risk was significantly high in DM patients with depression (AOR 2.05; 95% CI 1.02–4.12). Given the large number of patients with DM who are taking metformin worldwide, a double-blinded, prospective study is required to determine the long-term cognitive safety of metformin.


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