Sains Malaysiana 51(1)(2022):
209-215
http://doi.org/10.17576/jsm-2022-5101-17
Effect of Vitamin D on Aldose Reductase in Indonesian
Diabetic Polyneuropathy Patients: A Randomized Clinical Trial
(Kesan Vitamin D kepada Aldosa Reduktase dalam Kalangan
Pesakit Polineuropati Diabetes Indonesia: Suatu Ujian Klinikal Rambang)
AIDA FITRI1*, HASAN SJAHRIR1, ADANG BACHTIAR2 & MUHAMMAD ICHWAN3
1Department of Neurology, Faculty of
Medicine, Universitas Sumatera Utara, No. 5 Dr. Mansyur Road Medan, 20155 North
Sumatera, Indonesia
2Faculty of Public Health, University of
Indonesia, Lingkar Kampus Raya, Universitas Indonesia, Road Depok 16424, Indonesia
3Department of Pharmacology and
Therapeutic, Faculty of Medicine, Universitas Sumatera Utara, No. 5 Dr. Mansyur
Road Medan, 20155 North Sumatera, Indonesia
Received: 17 September 2019/Accepted: 19
April 2021
ABSTRACT
Aldose Reductase (AR) is an important
factor in the pathogenesis of several Diabetes Mellitus (DM) complications,
including diabetic neuropathy (DN). Vitamin D has a direct effect on the
pathogenesis of DN. Aldose reductase inhibition is an important element in the
prevention of DM complications. The objective of this paper was to assess the effect
of vitamin D on AR in Indonesian diabetic polyneuropathy (DPN) patients. This
cohort study was undertaken at Haji Adam Malik General Hospital Medan, North
Sumatera, Indonesia. In a double-blind, placebo-controlled, clinical trial,
eligible patients were randomized to receive vitamin D 50,000 IU/week or
placebo for 10 weeks. The primary end-point was mean changes of nerve
conduction velocity (NCV) from baseline and after 10 weeks of supplementation.
There was no significant correlation between mean changes of vitamin D and AR levels. There was significant correlation with negative direction and weak
strength between mean changes of AR level and NCV of motor Tibial nerve
(p<0.05; r=-0.337). There was significant correlation with positive
direction and moderate strength between mean changes of vitamin D level and NCV
of motor Median and Peroneal nerves, and motor and sensory Ulnar nerves (p<0.001;
r=0.438 – 0.527). In conclusion, vitamin D supplementation had no effect on AR level in Indonesian DPN patients. Higher AR level was correlated with decreased
NCV of motor Tibial nerve. Vitamin D supplementation improved NCV in DPN.
Keywords: Aldose
reductase; diabetic polyneuropathy; nerve conduction velocity; vitamin D
ABSTRAK
Aldosa Reduktase (AR) merupakan faktor
penting dalam patogenesis beberapa komplikasi Diabetes Mellitus (DM), termasuk
neuropati diabetes (ND). Vitamin D mempunyai kesan langsung kepada patogenesis
ND. Perencatan AR merupakan unsur penting dalam pencegahan komplikasi DM.
Tujuan kajian ini dijalankan adalah untuk menilai kesan vitamin D pada AR dalam
pesakit polineuropati diabetes (PND) Indonesia. Kajian kohort ini dilakukan di
Hospital Umum Haji Adam Malik Medan, Sumatera Utara, Indonesia. Dalam percubaan
klinikal gelap ganda, plasebo terkawal, pesakit yang layak menerima vitamin D
50.000 IU/minggu atau plasebo selama 10 minggu secara rambang. Titik akhir
utama adalah perubahan purata laju konduksi saraf daripada garis dasar dan selepas
10 minggu penambahan. Tiada korelasi yang signifikan antara perubahan purata
tahap vitamin D dengan AR. Terdapat korelasi yang signifikan dengan arah
negatif dan kekuatan lemah antara perubahan purata tahap AR dengan laju
konduksi saraf motor Tibial (p<0,05; r=-0,337). Terdapat korelasi yang
signifikan dengan arah positif dan kekuatan sederhana antara perubahan purata
tahap vitamin D dengan laju konduksi saraf motor Median dan Peroneal, dan saraf
motor dan sensori Ulnar (p<0,001; r=0.438 – 0.527). Secara
kesimpulannya, penambahan vitamin D tidak mempunyai kesan pada tahap AR dalam
kalangan pesakit PND Indonesia. Tahap AR yang tinggi dikaitkan dengan penurunan
laju konduksi saraf motor Tibial. Penambahan vitamin D menambah baik laju
konduksi saraf pada PND.
Kata kunci:
Aldosa reduktase; laju konduksi saraf; polineuropati diabetes; vitamin D
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*Corresponding
author; email: aida.fithrie@gmail.com
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