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العنوان
Evaluation of urinary Kidney injury molecule 1 (KIM-1) as a novel urinary biomarker for diabetic-nephropathy /
المؤلف
Mohammed, Mahmoud Saad.
هيئة الاعداد
باحث / محمود سعد محمد
مشرف / أسامة محمد كمال المنشاوي
مشرف / محمود حسن سيد خضر
مشرف / أسماء قاسم أحمد
الموضوع
Radiography, Medical. Radiography. Diagnosis, Surgical.
تاريخ النشر
2022.
عدد الصفحات
116 p. :
اللغة
الإنجليزية
الدرجة
الدكتوراه
التخصص
الطب الباطني
تاريخ الإجازة
1/1/2022
مكان الإجازة
جامعة المنيا - كلية الطب - الباطنة العامة
الفهرس
Only 14 pages are availabe for public view

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from 118

Abstract

Diabetes mellitus is a significant general medical problem influencing a great many individuals around the world. T2DM is progressively found in youngsters, teenagers, and more youthful grown-ups because of rising degrees of stoutness, actual idleness, and energy-thick weight control plans. Diabetic-nephropathy is one of the microvascular confusions related with DM, a determination alludes to explicit pathologic primary and useful changes found in the kidnys of patients with DM brings about a clinical show that is described by protienuria, hypertension, and moderate decreases in Kidny work. A serious diabetes inconvenience might advance to end-stage renal infection and is related with a high gamble of unexpected passing.
Screening of D N depends on egg whites discharge rate or assessed glomerular filtration rate that mostly mirrors the glomerular harm. Notwithstanding, cylindrical harm may likewise assume a significant part in D N, and urinary bio markrs of rounded injury are now accessible. Micro-albuminuria stays the highest quality level for early location of D N, it has been utilized as a symptomatic markr for more than thirty years for renal illness yet, late information proposes the failure of miniature albuminuria changes to predict the nephropathy movement in light of the fact that in something like 33% of patients renal downfall has previously followed. Thus, there is a change in outlook to novel bio markrs that would assist with foreseeing D N risk sufficiently early and conceivably forestall the event of ESKD.
Kidny injury particle 1 is such a bio markr for cylindrical injury, it is a sort 1 transmembrane glycoprotien, chiefly communicated at the apical layer of the proximal rounded cells yet in addition communicated in the glomerular epithelial cells. KIM1 had a few trademark highlights prescribed it to be utilized as an ideal markr of Kidny injury as the shortfall of KIM1 articulation in the ordinary Kidny and ex vivo room temperature dependability. In creature studies, KIM1 was a delicate bio markr of Kidny harm delivered by various causes and furthermore, human examinations affirmed KIM1 as a bio markr of intense Kidny injury or ongoing Kidny illnesses.
This is an imminent clinical preliminary that was at Mallawi General Hospital through about one year from January2017 to December 2017. The review incorporated a sum of 110 subjects who were ordered to :
 Bunch (I): (n=30): Included 30 T2DM patients with ACR < 30 mg/g (Normalbuminuric).
 Bunch (II): (n=25): Included 25 T2DM patients with ACR = 30-299 mg/g (Microalbuminuric).
 Bunch (III): (n=25): Included 25 T2DM patients with ACR ≥ 300 mg/g. (Albuminuric gathering).
 Bunch (IV): Control (n=30): Included 30 matched solid control subjects.
The review was performed to research the job of Kidny injury molecule-1 (KIM1) as a bio markr for early finding of diabetic-nephropathy, in patients with type 2 diabetes mellitus.
 Rejection models:
6) Age (under 18 or more than 70 years).
7) Type 1 DM, dynamic disease, cardiovascular breakdown, endocrinopathies other than T2DM, CKD from different causes than T2DM.
8) 24 hours pee test gathered inaccurately as well as ongoing urinary parcel contaminations.
9) Patients with a background marked by utilization of nephrotoxic drugs and NSAIDs during last 30 days.
10) Urinary stones, urinary lot a medical procedure or threatening sickness.
11) Patients with intense renal harm (counting intense fuel of CKD) and parchedness.
 Every one of the included members were exposed to the accompanying:
1. Full history taking.
2. General and actual assessments.
3. Research facility examinations (CBC, RBS, HbA1C, pee investigation, Kidny work, liver capacity, etc..).
4. A/C proportion.
5. G F R (by the CKD-EPI condition).
6. KIM1 assurance.
The acquired outcomes are summed up as follows:
The outcomes showed that there were no massive contrasts among bunches with respect to mature (p=0.56), sex (p=0.76), term of DM (p=0.25) and treatment of DM (p=0.72). While, the DM patients bunches had fundamentally higher BMI and number of cases with positive history of DM contrasted with control bunch.
The three T2DM bunches had fundamentally higher the two RBS and HBA1C contrasted with the benchmark group (p<0.01) while, there were no huge contrasts between the three DM gatherings.
Both microalbuminuric and albuminuric gatherings had essentially lower serum egg whites level contrasted with the normalbuminuric bunch and the benchmark group. While, inverse pattern of results was seen in createnine and urea levels, microalbuminuric and albuminuric gatherings had altogether higher createnine and urea levels contrasted with both the normalbuminuric bunch and the benchmark group.
Concerning protiens, the outcomes showed that method for AST were practically comparative in all gatherings with no huge contrasts while, the method for ALT were fundamentally higher in microalbuminuric and albuminuric gatherings contrasted with normoalbuminuric and control gatherings.
The outcomes showed that the most elevated pee egg whites mean was kept in the albuminuric gathering (101.8 ± 68.5 mg/l) followed with a tremendous distinction by the microalbuminuric bunch (53.2 ± 17.3 mg/l) and the most reduced pee egg whites values were kept in the normoalbuminuric bunch and the benchmark group (likewise with a huge contrast versus bunch II and III).
All gatherings contrasted essentially versus every others with respect to pee creatinin, the most elevated mean was seen in albuminoric bunch followed by microalbuminoric bunch followed by the normoalbuminoric bunch and the least worth was kept in the benchmark group.
The A/C proportion recorded massive distinction among all gatherings, the most noteworthy one was in albuminoric bunch (358.1 ± 76.8) trailed by the microalbuminoric bunch (54.6 ± 20.1) and followed by the normoalbuminoric bunch (16.8 ± 4.1) and the least proportion was seen in the benchmark group (11.6 ± 1.4).
The most elevated G F R was found in the benchmark group (121.1 ± 23.1 ml/min/1.73m2) followed with a massive distinction by the normoalbuminoric bunch (bunch I) (93.4 ± 22.6 ml/min/1.73m2) and the least G F R was kept in the albuminoric bunch (64.3 ± 22.5 ml/min/1.73m2) likewise with a huge contrast the normoalbuminoric bunch and the control.
The outcomes showed that the most noteworthy KIM1 was fundamentally higher in albuminoric bunch (0.98 ± 0.42 ng/ml) followed with a huge contrast by the microalbuminoric bunch (0.58 ± 0.31 ng/ml) but the normoalbuminoric bunch recorded a tremendous distinction versus the albuminoric bunch and the least KIM1 mean was seen in the benchmark group (0.26 ± 0.09 ng/ml) which varied essentially versus bunch (II) and (III). This uncovered that levels of KIM1 were expanded with the movement of diabetic-nephropathy. This uncovered that levels of KIM1 were expanded with the movement of diabetic-nephropathy.
There was an exceptionally huge positive relationship between KIM1 and A / C proportion (r = 0.43, p < 0.01) while, there was a profoundly critical negative relationship among KIM1 and G F R (r = -0.33, p < 0.01).