Serum CGRP, VIP, and PACAP usefulness in migraine: a case–control study in chronic migraine patients in real clinical practice

2020 ◽  
Vol 47 (9) ◽  
pp. 7125-7138
Author(s):  
Sara Pérez-Pereda ◽  
María Toriello-Suárez ◽  
Gonzalo Ocejo-Vinyals ◽  
Sandra Guiral-Foz ◽  
Jesús Castillo-Obeso ◽  
...  
2021 ◽  
Author(s):  
Miho Murashima ◽  
Tomohiro Tanaka ◽  
Atsuki Ide ◽  
Minamo Tomohiro Ono ◽  
Masashi Mizuno ◽  
...  

Abstract Background: Sodium-glucose cotransporter 2 inhibitors (SGLT2i) were reported to increase hemoglobin levels in short-term clinical trials. Whether it is also true in real clinical practice is unknown. Methods: This is a retrospective cohort study. Inclusion criterion was diabetics who visited our outpatient clinic from January 2019 to August 2020. Exposure of interest was the use of SGLT2i. Outcomes were hemoglobin levels. For the cross-sectional analyses, non-linear regression models were fitted with restricted cubic splines to investigate the association between hemoglobin levels and estimated glomerular filtration rate (eGFR) for users and non-users of SGLT2i. For the case-control study, cases (anemia defined as hemoglobin <120 g/L for men, <110 g/L for women or the use of erythropoiesis stimulating agents) and controls were matched by age, sex, and eGFR. Results: Among 2063 diabetics, 723 were on SGLT2i. In the cross-sectional analyses, hemoglobin levels were higher among SGLT2i users compared with non-users at eGFR >15 mL/min/1.73m2. For the case-control study, 197 cases and controls were matched. Conditional logistic regression showed that the use of SGLT2i was associated with significantly lower prevalence of anemia (OR: 0.35 [0.21-0.58]). Adjusted mean differences (95% CIs) in hemoglobin levels between users and propensity score-matched non-users of SGLT2i were 7.0 (3.0-10.0) g/L at 6 months. Among SGLT2i users, odds of increase in 6-month hemoglobin were similar across eGFR categories except for eGFR <15 mL/min/1.73m2.Conclusions: The use of SGLT2i was associated with higher hemoglobin levels and lower prevalence of anemia in real clinical practice.


2020 ◽  
Vol 21 (1) ◽  
pp. 123-130
Author(s):  
Enrique Martínez-Pías ◽  
David García-Azorín ◽  
Ane Minguez-Olaondo ◽  
Javier Trigo ◽  
Álvaro Sierra ◽  
...  

Rheumatology ◽  
2018 ◽  
Vol 57 (6) ◽  
pp. 1002-1010 ◽  
Author(s):  
Fiona A Pearce ◽  
Peter C Lanyon ◽  
Richard A Watts ◽  
Matthew J Grainge ◽  
Abhishek Abhishek ◽  
...  

2013 ◽  
Vol 14 (3) ◽  
pp. 278-281 ◽  
Author(s):  
Piero Barbanti ◽  
Cinzia Aurilia ◽  
Gabriella Egeo ◽  
Luisa Fofi ◽  
Nicola Vanacore

2018 ◽  
Vol 146 ◽  
pp. 172-179 ◽  
Author(s):  
C. Santucci ◽  
M. Franchi ◽  
L. Staszewsky ◽  
C. La Vecchia ◽  
R. Latini ◽  
...  

Odontology ◽  
2018 ◽  
Vol 107 (1) ◽  
pp. 90-95 ◽  
Author(s):  
Pablo Ameijeira ◽  
Yago Leira ◽  
Clara Domínguez ◽  
Rogelio Leira ◽  
Juan Blanco

2020 ◽  
Vol 3 ◽  
pp. 251581632092359
Author(s):  
Sara Pérez Pereda ◽  
María Toriello Suárez ◽  
Vicente González Quintanilla ◽  
Agustín Oterino

Background: Methylation of two CpG sites related to neuronal pentraxin II protein (NPTX2) and SH2 domain containing 5 protein (SH2D5), corresponding to two neuroplasticity genes, has been associated to headache chronification. We aimed to investigate the epigenetic modification of these two genes in chronic migraine (CM). Methods: We conducted a case–control study in which the DNA of 305 age- and sex-matched subjects classified according to the International Classification of Headache Disorders version beta (ICHD-III β) in CM (109), episodic migraine (EM; n = 98), and healthy controls (HC; 98) was analyzed. Real-time quantitative methylation-specific PCR was performed using specific methylation primers for two representative CpG sites within these genes. Results: We found no significant differences in methylation level between CM, EM, and HC in the first exon of the NPTX2 gene nor in the 5′ upstream region of the SH2D5 gene. Methylation level in the first exon of the NPTX2 showed a low correlation with age ( r = 0.266; p < 0.005). Conclusion: We did not find methylation level differences in analyzed regions related to NPTX2 and SH2D5 in our CM sample. Despite the potential relevance of neuroplasticity genes in headache chronification, we conclude that CM is a more heterogeneous clinical diagnosis than desired and that an epigenetic marker remains elusive.


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