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What Rheumatologists Learn from Nephrologists
1. What Rheumatologists can
learn from nephrologists?
Samar Tharwat Radwan
Lecturer of Internal Medicine
(Rheumatology & Immunology)
Mansoura University
3. Renal syndromes in patients with
rheumatic diseases
Asymptomatic
urinary
abnormalities
Nephrotic
syndrome
Acute nephritic
syndrome
Rapidly
progressive GN
Persistent
“subacute” GN
Renal vasculitis
Tubulointerstitial
nephritis
Chronic renal
failure (mild to
moderate)
Chronic renal
failure (severe)
4. The functional unit of the kidney is the nephron
The nephron consists of glomerulus followed by
a long network of tubules
The glomerulus has a highly vascular network
Various diseases that affect the vascular
system can affect the kidneys such as
• Systemic lupus erythematosus (SLE)
• Henoch-Schönlein purpura
• Churg-Strauss syndrome
• Microscopic polyangiitis
• ANCA associated granulomatous vasculitis
• Cryoglobulinemic vasculitis
5. Approach To Patients With Rheumatologic Disease
And Suspected Renal Involvement
• Careful Evaluation
• Thorough physical examination
(worsening HTN , edema)
• Directed laboratory assessment
6. Renal disease, unlike rheumatologic diseases,
has signs and symptoms that are not obvious
until late in the course of disease
So,
Routine screening for renal manifestations is
essential for preservation of renal function
12. In the lower range, small
increases in SCr reflect major
reductions in GFR
Half of renal function can be lost before SCr
exceeds the upper limits of normal
13. SCr is affected by other states with low muscle mass
Anorexia nervosa Amputations Chronic illnesses
14. EVALUATION OF RENAL DISEASE
Kidney function testing
Proteinuria
Hematuria
Other urinary microscopic
findings
Renal tubular dysfunction
Hypocomplementemia
Renal imaging
Kidney biopsy
15. Proteinuria
• Normal :< 150 mg of protein/day
• 20 mg :albumin
• Microalbuminuria:30 to 300 mg/day
• Macroalbuminuria >300 mg/day
• Nephrotic-range proteinuria >3.5
gm/day
16. Proteinuria identifies
• Patients with renal damage
• Those at risk for worsening renal disease
• Increased cardiovascular morbidity
18. Proteinuria
Overflow proteinuria
•Multiple myeloma
Tubular proteinuria
•< 2 g/day.
•Acute interstitial nephritis
immunosuppressive agents,
analgesics ,cryoglobulinemia,
and Sjögren syndrome
Glomerular proteinuria
•More severe
•SLE and rheumatoid arthritis
(RA)
19. Measurement of
proteinuria
• Dipstick testing:
inexpensive
screening
not quantify proteinuria
not detect nonalbumin
(light chain)
• A spot urine albumin-to-
creatinine ratio: < 30 mg/g
of albumin
The best sample is
the first urine of the
day
20. 500 mg/g consider :
a spot protein-to-creatinine ratio
OR
a 24-hour urine collection for proteinuria
27. If the definition of
hematuria is met, then the
provider must first rule out
reasons for
false-positive results,
including vigorous exercise
or menstruation.
38. EVALUATION OF RENAL DISEASE
Kidney function testing
Proteinuria
Hematuria
Other urinary microscopic
findings
Renal tubular dysfunction
Hypocomplementemia
Renal imaging
Kidney biopsy
39. RENAL IMAGING
Ultrasonography
• Noninvasive
• Kidney size
• Degree of echogenicity
• Anatomic abnormalities
• Obstruction
Assessment of the renal vasculature
• Doppler US
• Magnetic resonance /CT angiography
• Risk/benefit (contrast nephropathy)
Multiple microaneurysms within
the upper pole of the kidney
40. EVALUATION OF RENAL DISEASE
Kidney function testing
Proteinuria
Hematuria
Other urinary microscopic
findings
Renal tubular dysfunction
Hypocomplementemia
Renal imaging
Kidney biopsy
41. • Rapidly progressive GN (RPGN) (rapid
decline in kidney function/active urinary
sediment).. ANCA-related vasculitis,
and Henoch-Schönlein purpura
• Unexplained AKI
• Acute nephritic syndrome
• Persistent proteinuria
• Persistent hematuria
• Nephrotic syndrome
Indications
42. PATTERNS SEEN ON IMMUNOFLUORESCENCE MICROSCOPY
Linear
Anti-GBM disease
Goodpasture syndrome
Granular, “lumpy-bumpy
SLE,postinfectious GN
Pauci-immune
ANCA associated
granulomatous vasculitis
Wągrowska-Danilewicz et al. "Immunofluorescent evaluation of renal biopsy: current point of view." Polish Journal of Pathology (2010).
46. • 1827 SLE patients with followed from 1999 to 2012
• 10-year cumulative incidence of end-stage renal disease (ESRD) and death among
the patients with LN at 10.1% and 5.9%, respectively
47. Poor prognostic factors of LN
• Younger age
• Male gender
• Race
• Significant histologic changes
• Hypocomplementemia
• The presence of anticardiolipin
53. MIXED CONNECTIVE
TISSUE DISEASE
• Kidney involvement: 25% of cases
• Anti–U1-RNP antibody confers some renal
protective effect
• Individuals with more systemic manifestations
from MCTD appear to be at higher risk for
kidney involvement
• AKI/accelerated HTN/scleroderma kidney
• TTT: steroids ,ACEIs
57. POLYARTERITIS NODOSA
• Renal involvement :2/3 of cases
• The vessel wall: inflammatory segmental lesions ,aneurysms ,
rupture.
• HTN
• Ischemic renal lesions such as patchy cortical infarctions
• 50% of PAN cases : associated with hepatitis B
58. ANCA-
ASSOCIATED
VASCULITIDES
Renal manifestations include hematuria,
proteinuria, and rapidly progressive renal
failure.
• Positive ANCA
• The glomerular pathology is
indistinguishable
• Pulmonary lesions may develop later
• Systemic manifestations may develop
later
60. HENOCH-
SCHÖNLEIN
PURPURA
• Mild proteinuria and hematuria to
nephrotic syndrome or RPGN
• Mesangial proliferative GN
• Deposits of IGA in the mesangium
• Crescentic GN: less common
• Important cause of ESRD in children
61. PROGRESSIVE SYSTEMIC SCLEROSIS
(SCLERODERMA)
• Progressive mucoid thickening of the
walls and narrowing of the vascular
lumen of arteries
• Severe HTN and ischemic Kidney disease
• Scleroderma renal crisis 2%
• RAAS inhibition is the first line for
treatment of HTN in scleroderma
• Onion skin
• In normotensive scleroderma patients
:AAV or interstitial nephritis is considered
62. AMYLOIDOSIS
• Deposition of amyloid A (AA)
• Inflammatory rheumatologic
conditions :RA,JIA,AS,PsA,FMF
• C/P: nephrotic syndrome and
progressive renal failure
• Kidneys: larger
• TTT: anti-TNF agents
The most common of AA amyloidosis in the Western world and second most common worldwide is RA
Amyloid can also infiltrate the tubulointerstitial compartment and lead to renal tubular defects
66. ANTIPHOSPHOLIPID
SYNDROME
• Renal involvement: 9% - 25%
• Thrombosis of renal vessels : AKI,
proteinuria, hematuria, and HTN
• Thrombotic microangiopathy (TMA),
MCD, MGN, and FSGS
• Treatment is primarily anticoagulation
67. RENAL LESIONS WITH OTHER
RHEUMATIC DISEASES
• Poststreptococcal GN: rarely develops in individuals who contract acute
rheumatic fever because the nephritogenic and rheumatogenic strains of β-
hemolytic streptococci are different
• Psoriatic arthritis :amyloidosis
• Sarcoidosis: hypercalcemia , nephrolithiasis, interstitial nephritis with
granuloma formation
Here is a list of the renal syndromes that occur in persons with rheumatic diseases.
Rheumatologic diseases can lead to glomerular
injury and AKI directly, but recent treatment including nonsteroidal
antiinflammatory drugs can also be nephrotoxic and cause AKI
Another concern about the use of PCR
Proteinuria not only identifies
It is important to note
when proteinuria is present and when it is reduced; this protects the patient
against further loss of renal function
Overflow proteinuria occurs when an increased production of low-molecular
Proteins
Tubulointerstitial diseases affect renal tubules and the interstitium, leading
to decreased proximal reabsorption of proteins
Glomerular proteinuria occurs when there is damage to the filtration barrier
itself
Measurements of C3 and C4 are often used to narrow the differential diagnosis
of kidney diseases
Percutaneous kidney biopsy is an essential tool for determining the diagnosis,
prognosis, and treatment options for patients with kidney disease.