Pregled bibliografske jedinice broj: 49757
Proximal Diabetic Neuropathy - Response To Imunotherapy
Proximal Diabetic Neuropathy - Response To Imunotherapy // Diabetes / Weir, G. (ur.).
New York (NY): ADA, 1999. str. A148-A148 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 49757 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Proximal Diabetic Neuropathy - Response To Imunotherapy
Autori
Barada, Ante ; Reljanović, Miroslav ; Miličević, Zvonimir ; Ljubić, Spomenka ; Car, Nikica ; Benko, Bojan ; Vinik, Aron ; Metelko, Željko
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Diabetes
/ Weir, G. - New York (NY) : ADA, 1999, A148-A148
Skup
ADA, 59th Scientific Sessions
Mjesto i datum
San Diego (CA), Sjedinjene Američke Države, 19.06.1999. - 22.06.1999
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
PDN
Sažetak
Proximal diabetic neuropathy (PDN) has recently been shown to be immune mediated.
A prospective study was undertaken to investigate and compare the effect of immunomodulating (human immunoglobulin intravenous (IVIG)) and immunosuppression therapy (prednisone with azathioprine p.o.) in patients with subacute PDN, characterized by pronounced pain in the upper legs, atrophy of upper legs muscles, loss of predominantly pelvifemoral muscle strength as well a as marked reduction in femoral nerve motor conduction velocity (FNCV). Fourteen type 2 diabetic patients (mean age 64.4 yr., duration of diabetes 10 yr., duration of PDN 4.7 months, HbA1c 7.62 %) were included in the study. The patients were randomised; 9 patients received prednisone (1mg/kg p.o.) and azathioprine (100 mg) whereas 5 patients received IVIG (2.0 g/kg). Response to treatment was evaluated using visual analogue scale (VAS) for pain, muscle strength manual test (MMT) after 4, 8, 12, 24 weeks and FNCV was measured at 12 and 24 weeks.
Both therapies were found to be beneficial. Improvement was found for pain (baseline vs. follow- up VAS Z= 3.3, p=0.0001) muscle strength (baseline vs. follow/ up MMT Z= 3.3,p=0.0001) and FNCV (baseline vs. follow-up Z=3.2, p=0.0015).
The most pronounced improvement occurred in the first 4 weeks. Immunosuppression caused greater improvement in FVCV after 3 months as well as VAS after 2 months, compared to immunomodulation but the difference were not statistical significant.
Our results indicate that both immunosuppression and immunomodulation are efficient in subacute proximal diabetic neuropathy. Further studies are necessary to evaluate possible difference in long term outcomes between the therapies.
Proximal diabetic neuropathy (PDN) has recently been shown to be immune mediated.
A prospective study was undertaken to investigate and compare the effect of immunomodulating (human immunoglobulin intravenous (IVIG)) and immunosuppression therapy (prednisone with azathioprine p.o.) in patients with subacute PDN, characterized by pronounced pain in the upper legs, atrophy of upper legs muscles, loss of predominantly pelvifemoral muscle strength as well a as marked reduction in femoral nerve motor conduction velocity (FNCV). Fourteen type 2 diabetic patients (mean age 64.4 yr., duration of diabetes 10 yr., duration of PDN 4.7 months, HbA1c 7.62 %) were included in the study. The patients were randomised; 9 patients received prednisone (1mg/kg p.o.) and azathioprine (100 mg) whereas 5 patients received IVIG (2.0 g/kg). Response to treatment was evaluated using visual analogue scale (VAS) for pain, muscle strength manual test (MMT) after 4, 8, 12, 24 weeks and FNCV was measured at 12 and 24 weeks.
Both therapies were found to be beneficial. Improvement was found for pain (baseline vs. follow- up VAS Z= 3.3, p=0.0001) muscle strength (baseline vs. follow/ up MMT Z= 3.3,p=0.0001) and FNCV (baseline vs. follow-up Z=3.2, p=0.0015).
The most pronounced improvement occurred in the first 4 weeks. Immunosuppression caused greater improvement in FVCV after 3 months as well as VAS after 2 months, compared to immunomodulation but the difference were not statistical significant.
Our results indicate that both immunosuppression and immunomodulation are efficient in subacute proximal diabetic neuropathy. Further studies are necessary to evaluate possible difference in long term outcomes between the therapies.
Izvorni jezik
Engleski
POVEZANOST RADA
Projekti:
045006
Ustanove:
Klinika za dijabetes, endokrinologiju i bolesti metabolizma Vuk Vrhovac
Profili:
Nikica Car
(autor)
Željko Metelko
(autor)
Spomenka Ljubić
(autor)
Bojan Benko
(autor)
Miroslav Reljanović
(autor)
Ante Barada
(autor)