Journals / European Journal of General Medicine / 2013 / Cilt: 10 - Sayı: 4

İnflamatuar ve non-inflamatuar bel ağrılı hastalarda ağrı yoğunluğu ve oksidatif stres düzeylerinin değerlendirilmesi

Evaluation of pain ıntensity and oxidative stress levels in patients with ınflammatory and non-ınflammatory back pain

Pages
185–190
Publication Date
2022-10-18
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

All three back pain groups had significantly higher serum MDA levels compared to those of the control group (p

📌 3 Key Takeaways

🎯
Objective & Hypothesis:To investigate the relationship between pain threshold and oxidative stress levels in patients with acute and chronic inflammatory or non-inflammatory back pain.
📊
Key Findings & Data:A total of 137 patients were recruited for the study, including 33 acut back pain (32 lumbar disk herniation, 1 lumbar spondilosis) (16 men, 17 women), 35 with chronic back pain (33 lumbar disk herniation, 1 lumbar spondilosis, 1 sacralisation) (16 men, 19 women), 34 with ankylosing spondylitis (21 men, 13 women) (AS) and 35 without any back pain (15 men, 20 women).
💡
Conclusion & Impact:All three back pain groups had significantly higher serum MDA levels compared to those of the control group (p
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

To investigate the relationship between pain threshold and oxidative stress levels in patients with acute and chronic inflammatory or non-inflammatory back pain. A total of 137 patients were recruited for the study, including 33 acut back pain (32 lumbar disk herniation, 1 lumbar spondilosis) (16 men, 17 women), 35 with chronic back pain (33 lumbar disk herniation, 1 lumbar spondilosis, 1 sacralisation) (16 men, 19 women), 34 with ankylosing spondylitis (21 men, 13 women) (AS) and 35 without any back pain (15 men, 20 women). The visual analogue scale (VAS) was used to evaluate pain levels and algometry was used to evaluate the pain threshold in all cases. In addition, serum malondialdehyde (MDA) levels were assessed in all patients. The mean ages for groups 1, 2, 3, and 4 were 40.3±10.3, 39.9±9.7, 40.6±10.4, and 38.5±8.1 years, respectively. There was no significant difference between the ages of the groups (p=0.851) (Table 1). The VAS scores of all groups were significantly higher compared to the control group. Particularly, the acute and chronic back pain groups had significantly higher VAS scores than those of the AS group. All three back pain groups had significantly higher serum MDA levels compared to those of the control group (p

Özet

Akut ve kronik inflamatuar veya non-inflamatuar bel ağrılı hastalarda ağrı eşiği ve oksidatif stres düzeyleri arasındaki ilişkiyi değerlendirmek amaçlandı. 33 akut bel ağrılı (16 erkek, 17 kadın), 45 kronik bel ağrılı (16 erkek, 19 kadın), 34 Ankilozan spondil- itli (21 erkek, 13 kadın) ve 35 sağlıklı gönüllü (15 erkek, 20 kadın) olmak üzere toplam 137 birey çalışmaya dahil edildi. Bütün bireylerin ağrı düzeyleri VAS ile, ağrı eşikleri ise algometri ile değerlendirildi. İlaveten, tüm bireylerin serum malondialdehyde (MDA) düzeyleri değerlendirildi. 1, 2, 3. ve 4. grupların ortalama yaşları 40.3 ± 10.3, 39.9 ± 9.7, 40.6 ± 10.4 ve 38.5 ± 8.1 yıl idi, Grupların yaşları arasında istatistiksel olarak anlamlı fark yoktu (p=0.851) (Tablo 1). Bel ağrılı grupların herbiri kontrol grubu ile karşılaştırıldığında anlamlı şekilde daha yüksek MDA düzeylerine sahipti (p

🔖

Cite This Article

SOĞUT, E., İNANIR, A., İNANIR, S., AYAN, M. (2022). İnflamatuar ve non-inflamatuar bel ağrılı hastalarda ağrı yoğunluğu ve oksidatif stres düzeylerinin değerlendirilmesi. European Journal of General Medicine, Cilt: 10 - Sayı: 4, 185–190. https://ajindex.com/articles/511007

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (1)

  1. Kandel ER, Schwartz JH, Jessell TM. Learning and mem- ory in Principles or neural science, McGraw Hill Company New York, 2000:1227-46 2.Cast-Baril WL, Frymoyer JW. Identifying patients at risk of becoming disabled because of low back pain. Spine 1991;16: 605-7 3.Goertz MN (1990) Prognostic indicators for acute low back pain. Spine 15:1307-10 4.Volat JP (1994) Low back pain, sciatica and lumbar inter- vertebral disc disease. Rheum Europ 2:55-8 5.Buchbinder R, jolley D, Wyatt M (2001) Population based intervention to change back pain beliefs and disability: three part evalution. Br Med J 322:1516-20 6.Yazici C, Köse K, Calis M et al (2004) Protein oxidation sta- tus in patients with ankylosing spondylitis. Rheumatology (Oxf) 43:1235-9 7.Koehler L, Kuipers JG, Zeidler H (2000) Managing sero- negative spondyloarthritis. Rheumatology 39:360-8. 8.Ha HC, Sirisoma NS, Kuppusamy P et al (1998) The natural polyamine spermine functions directly as a free radical scavenger. Proc Natl Acad Sci USA 95:11140–5 9. Halliwell B, Vitamin C (1999) Poison, prophylactic or pan- acea? Trends Biochem Sci 24:255–9 10. Jenkinson SG (1988) Oxygen toxicity. J Intensive Care Med 3:137–52 11. Jackson MJ, O Farrell SO (1993) Free radicals and muscle damage. Br Med Bull 49:630–41 12. Beck AT, Ward CH, Mendelson M et al (1961) An Inventory For Measuring Depression. Arch Gen Psychiatry 4:561-71. 13. Cast-Baril WL, Frymoyer JW (1991) Identifying patients at risk of becoming disabled because of low back pain. Spine 16: 605-7. 14. Brosseau L, Milne S, Robinson V at al (2002) Efficacy of the transcutaneous electrical nevre stimulation for the treatment of chronic low back pain. Spine 27:596-603 15. Ho KJ, Chen PQ, Chang CY et al (2000) The oxidative me- tabolism of circulating phagocytes in ankylosing spondy- litis: determination by whole blood chemiluminescence. Ann Rheum Dis 59:338–41 16. Van der Unden (1997) Ankylosing spondylitis. İn: Kelley WN, Haris ED, Ruddy S, Sledge CB. Texbook of Rheumatology. Philâdelphia: W.B. Saunders Company 969-82 17. Han D, Canali R, Rettori D et al (2003) Effect of gluta- thione depletion on sites and topology of superoxide and hydrogen peroxide production in mitochondria, Mol Pharmacol 64:1136-44 18. Tunc O, Bakos HW, Tremellen K (2011) Impact of body mass index on seminal oxidative stress. Andrologia 43:121-8. 19. Codoñer-Franch P, Tavárez-Alonso S, Murria-Estal R et al (2011) Nitric oxide production is increased in severely obese children and related to