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Nörogörüntüleme ile Migren Patofizyolojisinin Nörokimyasal ve Yapısal Özellikleri

Yıl 2024, Cilt: 1 Sayı: 2 (Aralık), 1 - 10, 26.12.2024

Öz

Kronik migren, migren hastalarının sosyoekonomik işlevleri ve yaşam kaliteleri üzerinde olumsuz etkisi olan, oldukça kısıtlayıcı bir hastalıktır. Kronik migren genellikle atak sıklığı giderek artan epizodik migrenden gelişir ve migrenin bir spektrum bozukluğu olduğu görüşünü destekler. Migrenin kronikleşmesinden sorumlu patofizyolojik mekanizmalar tam olarak anlaşılamamıştır. Epizodik migrende olduğu gibi, kronik migren hastalarında da kortikal ve subkortikal ağrıyla ilişkili beyin bölgelerinde yaygın işlevsel ve yapısal değişiklikler görülmektedir. Bununla birlikte, kronik migren hastaları ağrı engelleyici ağda daha belirgin bir işlev bozukluğu ve merkezi ağrı yollarında artmış bir duyarlılık yaşarlar, bu da migren ataklarına karşı daha yüksek duyarlılığı açıklayabilir. Görüntüleme çalışmaları, pons ve hipotalamus gibi migren ataklarının oluşumunda kilit rol oynayan beyin bölgelerinin migrenin kronikleşmesinde de rol oynayabileceğini vurgulamıştır. Beyindeki değişikliklerin migren hastalarını kronikleşmeye yatkın hale getiren biyobelirteçler mi olduğu yoksa artan baş ağrısı sıklığına karşı adaptif veya maladaptif yanıtları mı yansıttığı hala tartışma konusudur. Kronik migreni önleyici tedavilerin merkezi etki mekanizmaları ve hastaların tedavi yanıtını öngörebilecek görüntüleme biyobelirteçleri de araştırılmıştır.Bu derlemenin amacı, nörokimyasal ve yapısal analizleri içeren güncel literatürü gözden geçirmek ve sentezlemektir. Kronik migren patofizyolojisini araştırmak, klinik sonuçlarını daha fazla tartışmak ve tedavide kullanılabilirliğini değerlendirmek için beyin görüntülemesi kullanılmıştır.

Kaynakça

  • Al-Salama, Z. T. (2021). Metyrapone in Cushing’s Syndrome: A Profile of its Use. Drugs & Therapy Perspectives, 37(9), 393-406.
  • Braun, L. T., & Reincke, M. (2020). What is The Role of Medical Therapy in Adrenal-Dependent Cushing’s Syndrome? Best Practice & Research Clinical Endocrinology & Metabolism, 34(3), 101376.
  • Castinetti, F. (2023). Pharmacological Treatment of Cushing’s Syndrome. Archives of Medical Research, 102908.
  • Daniel, E., & Newell-Price, J. D. (2015). Therapy of Endocrine Disease: Steroidogenesis Enzyme Inhibitors in Cushing’s Syndrome. European Journal of Endocrinology, 172(6), R263- R280.
  • Rogóz, Z., Skuza, G., Wójcikowski, J., & Daniel, W. A. (2003). Effects of Combined Treatment with Imipramine and Metyrapone in The Forced Swimming Test in Rats. Behavioral And Pharmacokinetic Studies. Polish journal of pharmacology, 55(6), 993–999.
  • Fleseriu, M., Auchus, R., Bancos, I., Ben-Shlomo, A., Bertherat, J., Biermasz, N. R., Boguszewski, C. L., Bronstein, M. D., Buchfelder, M., Carmichael, J. D., Casanueva, F. F., Castinetti, F., Chanson, P., Findling, J., Gadelha, M., Geer, E. B., Giustina, A., Grossman, A., Gurnell, M., Ho, K., … & Biller, B. M. K. (2021). Consensus on Diagnosis and Management of Cushing’s Disease: A Guideline Update. The Lancet. Diabetes & endocrinology, 9(12), 847–875.
  • Hakami, O. A., Ahmed, S., & Karavitaki, N. (2021). Epidemiology and Mortality of Cushing’s syndrome. Best Practice & Research Clinical Endocrinology & Metabolism, 35(1), 101521.
  • Headache Classification Committee of the International Headache Society (IHS) The International Classification of Headache Disorders, 3rd edition. (2018). Cephalalgia : An International Journal of Headache, 38(1), 1–211.
  • Healy, D. G., Harkin, A., Cryan, J. F., Kelly, J. P., & Leonard, B. E. (1999). Metyrapone Displays Antidepressant-Like Properties in Preclinical Paradigms. Psychopharmacology, 145, 303- 308.
  • Igaz, P., Tombol, Z., Szabo, P., Liko, I., & Racz, K. (2008). Steroid Biosynthesis Inhibitors in The Therapy of Hypercortisolism: Theory and Practice. Current Medicinal Chemistry, 15(26), 2734-2747.
  • Jeffcoate, W., Silverstone, J., Edwards, C., & Besser, G. (1979). Psychiatric Manifestations of Cushing’s Syndrome: Response to Lowering of Plasma Cortisol. QJM: An International Journal of Medicine, 48(3), 465-472.
  • Johnson, D. A., Grant, E. J., Ingram, C. D., & Gartside, S. E. (2007). Glucocorticoid Receptor Antagonists Hasten and Augment Neurochemical Responses to A Selective Serotonin Reuptake Inhibitor Antidepressant. Biological Psychiatry, 62(11), 1228-1235.
  • Lacroix, A., Feelders, R. A., Stratakis, C. A., & Nieman, L. K. (2015). Cushing’s Syndrome. The lancet, 386(9996), 913-927.
  • Levin, J., Zumoff, B., & Fukushima, D. K. (1978). Extraadrenal Effects of Metyrapone in Man. The Journal of Clinical Endocrinology & Metabolism, 47(4), 845-849.
  • Nieman, L. K., Biller, B. M., Findling, J. W., Murad, M. H., Newell-Price, J., Savage, M. O., & Tabarin, A. (2015). Treatment of Cushing’s Syndrome: An Endocrine Society Clinical Practice Guideline. The Journal of Clinical Endocrinology & Metabolism, 100(8), 2807- 2831.
  • Pivonello, R., Ferrigno, R., De Martino, M. C., Simeoli, C., Di Paola, N., Pivonello, C., Barba, L., Negri, M., De Angelis, C., & Colao, A. (2020). Medical Treatment of Cushing’s Disease: An Overview of The Current and Recent Clinical Trials. Frontiers in Endocrinology, 11, 648.
  • Raven, P., O’Dwyer, A.-M., Taylor, N., & Checkley, S. (1996). The Relationship Between The Effects of Metyrapone Treatment on Depressed Mood and Urinary Steroid Profiles. Psychoneuroendocrinology, 21(3), 277-286.
  • Rigel, D. F., Fu, F., Beil, M., Hu, C.-W., Liang, G., & Jeng, A. Y. (2010). Pharmacodynamic and Pharmacokinetic Characterization of The Aldosterone Synthase Inhibitor FAD286 in Two Rodent Models of Hyperaldosteronism: Comparison with The 11β-Hydroxylase Inhibitor Metyrapone. Journal of Pharmacology and Experimental Therapeutics, 334(1), 232-243.
  • Sampath-Kumar, R., Yu, M., Khalil, M., & Yang, K. (1997). Metyrapone is a Competitive Inhibitor of 11β-Hydroxysteroid Dehydrogenase Type 1 Reductase. The Journal of Steroid Biochemistry and Molecular Biology, 62(2-3), 195-199.
  • Schöneshöfer, M., Schefzig, B., & Arabin, S. (1980). Short-Term Kinetics of Serum Adrenal Steroids and Plasma ACTH After A Single Dose of Metyrapone in Man. Journal of Endocrinological Investigation, 3, 229-236.
  • Simões Corrêa Galendi, J., Correa Neto, A. N. S., Demetres, M., Boguszewski, C. L., & Nogueira, V. D. S. N. (2021). Effectiveness of Medical Treatment of Cushing’s Disease: A Systematic Review and Meta-Analysis. Frontiers in Endocrinology, 12, 732240.

Neurochemical and Structural Characteristics of Migraine Pathophysiology with Neuroimaging

Yıl 2024, Cilt: 1 Sayı: 2 (Aralık), 1 - 10, 26.12.2024

Öz

Chronic migraine is a highly restrictive disease that has a deleterious impact on the socioeconomic functioning and quality of life of those affected. The development of chronic migraine from episodic migraine is typically characterised by an increase in the frequency of attacks, which lends support to the view that migraine can be considered a spectrum disorder. The precise pathophysiological mechanisms responsible for the chronicity of migraine remain unclear. Similarly, chronic migraine patients exhibit extensive functional and structural alterations in cortical and subcortical regions associated with pain perception. However, patients with chronic migraine exhibit a more pronounced dysfunction in the pain inhibitory network and an increased sensitivity in central pain pathways, which may explain their higher susceptibility to migraine attacks. Imaging studies have highlighted the potential involvement of brain regions that are crucial for the onset of migraine attacks, such as the pons and hypothalamus, in the chronicity of migraine. The question of whether changes in the brain are biomarkers predisposing migraineurs to chronicity or reflect adaptive or maladaptive responses to increased headache frequency remains a topic of debate. The central mechanisms of action of preventive treatments for chronic migraine and imaging biomarkers that may predict patients' treatment response have also been investigated. The aim of this review is to synthesise the current literature on neurochemical and structural analyses. Brain imaging has been used to investigate the pathophysiology of chronic migraine, to further discuss its clinical implications and to assess its utility in treatment.

Kaynakça

  • Al-Salama, Z. T. (2021). Metyrapone in Cushing’s Syndrome: A Profile of its Use. Drugs & Therapy Perspectives, 37(9), 393-406.
  • Braun, L. T., & Reincke, M. (2020). What is The Role of Medical Therapy in Adrenal-Dependent Cushing’s Syndrome? Best Practice & Research Clinical Endocrinology & Metabolism, 34(3), 101376.
  • Castinetti, F. (2023). Pharmacological Treatment of Cushing’s Syndrome. Archives of Medical Research, 102908.
  • Daniel, E., & Newell-Price, J. D. (2015). Therapy of Endocrine Disease: Steroidogenesis Enzyme Inhibitors in Cushing’s Syndrome. European Journal of Endocrinology, 172(6), R263- R280.
  • Rogóz, Z., Skuza, G., Wójcikowski, J., & Daniel, W. A. (2003). Effects of Combined Treatment with Imipramine and Metyrapone in The Forced Swimming Test in Rats. Behavioral And Pharmacokinetic Studies. Polish journal of pharmacology, 55(6), 993–999.
  • Fleseriu, M., Auchus, R., Bancos, I., Ben-Shlomo, A., Bertherat, J., Biermasz, N. R., Boguszewski, C. L., Bronstein, M. D., Buchfelder, M., Carmichael, J. D., Casanueva, F. F., Castinetti, F., Chanson, P., Findling, J., Gadelha, M., Geer, E. B., Giustina, A., Grossman, A., Gurnell, M., Ho, K., … & Biller, B. M. K. (2021). Consensus on Diagnosis and Management of Cushing’s Disease: A Guideline Update. The Lancet. Diabetes & endocrinology, 9(12), 847–875.
  • Hakami, O. A., Ahmed, S., & Karavitaki, N. (2021). Epidemiology and Mortality of Cushing’s syndrome. Best Practice & Research Clinical Endocrinology & Metabolism, 35(1), 101521.
  • Headache Classification Committee of the International Headache Society (IHS) The International Classification of Headache Disorders, 3rd edition. (2018). Cephalalgia : An International Journal of Headache, 38(1), 1–211.
  • Healy, D. G., Harkin, A., Cryan, J. F., Kelly, J. P., & Leonard, B. E. (1999). Metyrapone Displays Antidepressant-Like Properties in Preclinical Paradigms. Psychopharmacology, 145, 303- 308.
  • Igaz, P., Tombol, Z., Szabo, P., Liko, I., & Racz, K. (2008). Steroid Biosynthesis Inhibitors in The Therapy of Hypercortisolism: Theory and Practice. Current Medicinal Chemistry, 15(26), 2734-2747.
  • Jeffcoate, W., Silverstone, J., Edwards, C., & Besser, G. (1979). Psychiatric Manifestations of Cushing’s Syndrome: Response to Lowering of Plasma Cortisol. QJM: An International Journal of Medicine, 48(3), 465-472.
  • Johnson, D. A., Grant, E. J., Ingram, C. D., & Gartside, S. E. (2007). Glucocorticoid Receptor Antagonists Hasten and Augment Neurochemical Responses to A Selective Serotonin Reuptake Inhibitor Antidepressant. Biological Psychiatry, 62(11), 1228-1235.
  • Lacroix, A., Feelders, R. A., Stratakis, C. A., & Nieman, L. K. (2015). Cushing’s Syndrome. The lancet, 386(9996), 913-927.
  • Levin, J., Zumoff, B., & Fukushima, D. K. (1978). Extraadrenal Effects of Metyrapone in Man. The Journal of Clinical Endocrinology & Metabolism, 47(4), 845-849.
  • Nieman, L. K., Biller, B. M., Findling, J. W., Murad, M. H., Newell-Price, J., Savage, M. O., & Tabarin, A. (2015). Treatment of Cushing’s Syndrome: An Endocrine Society Clinical Practice Guideline. The Journal of Clinical Endocrinology & Metabolism, 100(8), 2807- 2831.
  • Pivonello, R., Ferrigno, R., De Martino, M. C., Simeoli, C., Di Paola, N., Pivonello, C., Barba, L., Negri, M., De Angelis, C., & Colao, A. (2020). Medical Treatment of Cushing’s Disease: An Overview of The Current and Recent Clinical Trials. Frontiers in Endocrinology, 11, 648.
  • Raven, P., O’Dwyer, A.-M., Taylor, N., & Checkley, S. (1996). The Relationship Between The Effects of Metyrapone Treatment on Depressed Mood and Urinary Steroid Profiles. Psychoneuroendocrinology, 21(3), 277-286.
  • Rigel, D. F., Fu, F., Beil, M., Hu, C.-W., Liang, G., & Jeng, A. Y. (2010). Pharmacodynamic and Pharmacokinetic Characterization of The Aldosterone Synthase Inhibitor FAD286 in Two Rodent Models of Hyperaldosteronism: Comparison with The 11β-Hydroxylase Inhibitor Metyrapone. Journal of Pharmacology and Experimental Therapeutics, 334(1), 232-243.
  • Sampath-Kumar, R., Yu, M., Khalil, M., & Yang, K. (1997). Metyrapone is a Competitive Inhibitor of 11β-Hydroxysteroid Dehydrogenase Type 1 Reductase. The Journal of Steroid Biochemistry and Molecular Biology, 62(2-3), 195-199.
  • Schöneshöfer, M., Schefzig, B., & Arabin, S. (1980). Short-Term Kinetics of Serum Adrenal Steroids and Plasma ACTH After A Single Dose of Metyrapone in Man. Journal of Endocrinological Investigation, 3, 229-236.
  • Simões Corrêa Galendi, J., Correa Neto, A. N. S., Demetres, M., Boguszewski, C. L., & Nogueira, V. D. S. N. (2021). Effectiveness of Medical Treatment of Cushing’s Disease: A Systematic Review and Meta-Analysis. Frontiers in Endocrinology, 12, 732240.
Toplam 21 adet kaynakça vardır.

Ayrıntılar

Birincil Dil Türkçe
Konular Klinik Nöropsikoloji
Bölüm Derlemeler
Yazarlar

Hatice Cakir 0009-0009-5135-6561

Osman Kağan Çakır 0009-0008-2549-0321

Yayımlanma Tarihi 26 Aralık 2024
Gönderilme Tarihi 7 Ekim 2024
Kabul Tarihi 26 Kasım 2024
Yayımlandığı Sayı Yıl 2024 Cilt: 1 Sayı: 2 (Aralık)

Kaynak Göster

APA Cakir, H., & Çakır, O. K. (2024). Nörogörüntüleme ile Migren Patofizyolojisinin Nörokimyasal ve Yapısal Özellikleri. Erzincan Binali Yıldırım Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi, 1(2 (Aralık), 1-10.