Tab Application Banner
  • Users Online: 2487
  • Home
  • Print this page
  • Email this page
Home About us Editorial board Ahead of print Current issue Search Archives Submit article Instructions Subscribe Contacts Login 


 
 Table of Contents  
IMAGES IN RHEUMATOLOGY
Year : 2021  |  Volume : 16  |  Issue : 1  |  Page : 109-110

A case of arterial calcification due to deficiency of CD73


1 Department of General Medicine, KMCT Medical College, Calicut, Kerala, India
2 Department of Radiodiagnosis, KMCT Medical College, Calicut, Kerala, India

Date of Submission19-Aug-2020
Date of Acceptance26-Sep-2020
Date of Web Publication23-Mar-2021

Correspondence Address:
Dr. Reeta James
Department of General Medicine, KMCT Medical College, Manassery, Kozhikode - 673 602, Kerala
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/injr.injr_228_20

Rights and Permissions
  Abstract 


Keywords: Arterial Calcification, CD73, NT5E gene


How to cite this article:
James R, Paul BJ, Vasu C K. A case of arterial calcification due to deficiency of CD73. Indian J Rheumatol 2021;16:109-10

How to cite this URL:
James R, Paul BJ, Vasu C K. A case of arterial calcification due to deficiency of CD73. Indian J Rheumatol [serial online] 2021 [cited 2021 Dec 2];16:109-10. Available from: https://www.indianjrheumatol.com/text.asp?2021/16/1/109/301574



We report the case of a 43-year-old male born out of nonconsanguineous marriage who presented with recurrent pain and swelling of the small joints of both hands and pain in both knees. On examination, there was tenderness of the proximal interphalangeal joints (PIPJs), distal interphalangeal (IP) joints, and wrist with palpable Heberden's nodes in both hands [Figure 1]a. Pedigree analysis showed that no other family member was affected. Laboratory investigations revealed normal blood counts with erythrocyte sedimentation rate of 30 mm/1st h. Rheumatoid factor and anti-cyclic citrullinated peptide were negative. Serum alkaline phosphatase was within normal limits. Serum calcium level was 9.8 mg/dL and serum phosphorus level was 4.01 mg/dL.
Figure 1: (a) Hands of the patient showing swelling of the interphalangeal joints and Heberden's nodes. (b) X-ray of the hands (antero-posterior view) showing periarticular calcification and osteoarthritic changes

Click here to view


X-ray (antero-posterior [AP] view) of the right hand [Figure 1]b showed capsular and periarticular calcification at the PIPJ of the middle finger, calcification of the 2nd metacarpophalangeal (MCP) joint and first IP joint, calcification of the ulnar collateral ligament, and osteoarthritis-like changes in these joints. X-ray (AP view) of the left hand [Figure 1]b showed capsular and periarticular calcification of the 2nd and 3rd PIPJs and base of the 1st MCP joint, calcific foci in the radiocarpal joint, and calcification of the ulnar collateral ligament with advanced osteoarthritis of these joints. X-ray of the knee [Figure 2] showed extensive calcification of the popliteal artery. There were no signs of distal ischemia, and all peripheral pulses were equally palpable. Arterial and venous Doppler study of both lower limbs showed normal flow.
Figure 2: X-ray of the knee (antero-posterior and lateral view) showing extensive calcification of the popliteal artery

Click here to view


The radiological picture along with arterial calcification and clinical presentation seemed to be highly suggestive of arterial calcification due to deficiency of CD73 (ACDC). Genetic analysis of the patient by clinical exome sequencing revealed homozygous mutation, c1465_1477 del (p. Met4891lefsTer3) on exon 8 of NT5E gene, thereby confirming the diagnosis of ACDC. Genetic analysis of his siblings could not be done due to financial constraints and his parents were no more. Our patient was initiated on 70 mg of alendronate weekly and is on follow-up.

ACDC is a rare autosomal recessive genetic disorder caused by mutation in the NT5E gene, which results in extensive calcification of vessels below the diaphragm, notably the large lower extremity arteries and small joint capsules of the hands and feet.[1] Also known as “calcification of joints and arteries” (CALJA) syndrome, the late-onset profound calcification spares arteries in the trunk and the coronary circulation. Only seven cases of CALJA were reported till 2011, when St Hilaire et al. identified disease-causing NT5E gene mutations in three families with CALJA.[1] Thereafter, about 13 cases have been reported from six families.[2] NT5E gene encodes for CD73, a membrane-bound ecto 5'-nucleotidase, responsible for extracellular Adenosine Triphosphate (ATP) metabolism throughout the body. Adenosine monophosphate (AMP) and pyrophosphate are formed from ATP by the action of ectonucleotide pyrophosphatase-phosphodiesterase 1. Normally, CD73 binds to AMP and converts it to adenosine and inorganic phosphate. Tissue nonspecific alkaline phosphatase (TNAP) is responsible for the breakdown of pyrophosphate throughout the body. Calcification process depends on the levels of pyrophosphate, which is crucial for the inhibition of calcification. TNAP is inhibited by adenosine. NT5E mutation results in little or no functional CD73, ultimately resulting in excessive calcification. The predilection for lower extremity arteries is attributed to the pattern of distribution of adenosine receptors.[3] Intermittent arthritis resembling basic calcium phosphate crystal deposition disease and early-onset osteoarthritis are found to be characteristics of ACDC.[4] Bisphosphonates maybe beneficial in patients with CD73 deficiency, as they are pyrophosphate analogs and hence can inhibit tissue calcification.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
  References Top

1.
St Hilaire C, Ziegler SG, Markello TC, Brusco A, Groden C, Gill F, et al. NT5E mutations and arterial calcifications. N Engl J Med 2011;364:432-42.  Back to cited text no. 1
    
2.
Yoshioka K, Kuroda S, Takahashi K, Sasano T, Furukawa T, Matsumura A. Calcification of joints and arteries with novel NT5E mutations with involvement of upper extremity arteries. Vasc Med 2017;22:541-3.  Back to cited text no. 2
    
3.
Yang D, Zhang Y, Nguyen HG, Koupenova M, Chauhan AK, Makitalo M, et al. The A2B adenosine receptor protects against inflammation and excessive vascular adhesion. J Clin Invest 2006;116:1913-23.  Back to cited text no. 3
    
4.
Ichikawa N, Taniguchi A, Kaneko H, Kawamoto M, Sekita C, Nakajima A, et al. Arterial calcification due to deficiency of CD73 (ACDC) as one of rheumatic diseases associated with periarticular calcification. J Clin Rheumatol 2015;21:216-20.  Back to cited text no. 4
    


    Figures

  [Figure 1], [Figure 2]



 

Top
 
 
  Search
 
Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
 Related articles
Access Statistics
Email Alert *
Add to My List *
* Registration required (free)

 
  In this article
Abstract
References
Article Figures

 Article Access Statistics
    Viewed1359    
    Printed33    
    Emailed0    
    PDF Downloaded101    
    Comments [Add]    

Recommend this journal


[TAG2]
[TAG3]
[TAG4]