Biology:McDonald criteria

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McDonald criteria
Medical diagnostics
Monthly multiple sclerosis anim cropped no text.gif
Animation showing dissemination of multiple sclerosis lesions in time and space as demonstrated by monthly MRI studies along a year
PurposeDiagnosis of MS

The McDonald criteria are diagnostic criteria for multiple sclerosis (MS). These criteria are named after neurologist W. Ian McDonald who directed an international panel in association with the National Multiple Sclerosis Society (NMSS) of United States and recommended revised diagnostic criteria for MS in April 2001. These new criteria intended to replace the Poser criteria and the older Schumacher criteria. They have undergone revisions in 2005,[1] 2010[2] and 2017.[3]

They maintain the Poser requirement to demonstrate "dissemination of lesions in space and time" (DIS and DIT)[2] but they discourage the previously used Poser terms such as "clinically definite" and "probable MS", and propose as diagnostic either "MS", "possible MS", or "not MS".[4]

The McDonald criteria maintained a scheme for diagnosing MS based solely on clinical grounds but also proposed for the first time that when clinical evidence is lacking, magnetic resonance imaging (MRI) findings can serve as surrogates for dissemination in space (DIS) and/or time (DIT) to diagnose MS.[5] The criteria try to prove the existence of demyelinating lesions, by image or by their effects, showing that they occur in different areas of the nervous system (DIS) and that they accumulate over time (DIT). The McDonald criteria facilitate the diagnosis of MS in patients who present with their first demyelinating attack and significantly increase the sensitivity for diagnosing MS without compromising the specificity.[5]

The McDonald criteria for the diagnosis of multiple sclerosis were revised first in 2005 to clarify exactly what is meant by an "attack", "dissemination" and a "positive MRI", etc.[1] Later they were revised again in 2017.[6]

McDonald criteria are the standard clinical case definition for MS and the 2010 version is regarded as the gold standard test for MS diagnosis.[citation needed]

Diagnostic Criteria

Clinical Presentation Additional Data Needed
* 2 or more attacks (relapses)
* 2 or more objective clinical lesions 		None; clinical evidence will suffice (additional evidence desirable but must be consistent with MS)
* 2 or more attacks
* 1 objective clinical lesion 		Dissemination in space, demonstrated by:
* MRI
* or further clinical attack involving different site
* 1 attack
* 2 or more objective clinical lesions 		Dissemination in time, demonstrated by:
* MRI
* or second clinical attack
* or CSF-specific oligoclonal bands
* 1 attack
* 1 objective clinical lesion
(monosymptomatic presentation) 		Dissemination in space demonstrated by:
* MRI
* or an additional clinical attack implicating a different CNS site
and
Dissemination in time demonstrated by:
* MRI
* or second clinical attack
* or CSF-specific oligoclonal bands
Insidious neurological progression
suggestive of MS
(primary progressive MS) 		One year of disease progression (retrospectively or prospectively determined) and

Two of the following:

a. Positive brain MRI (nine T2 lesions or four or more T2 lesions with positive VEP)
b. Positive spinal cord MRI (two focal T2 lesions)
c. Positive CSF

They discourage the previously used terms such as "clinically definite" and "probable MS", and propose as diagnostic variants like "MS", "possible MS", or "not MS",[4] though these terms change between revisions. As of 2017 revision The term ‘possible MS’ was added for people with a typical clinically isolated syndrome who did not meet the criteria.[7]

Criticism

Pathology is generally regarded as the gold standard in defining different forms of inflammatory demyelinating diseases.[8]

Specificity of the McDonald criteria is low due to the fact that the nature of the lesions is not considered, but only their dissemination. None of the criteria are MS-specific. In order to reduce false positives, McDonald et al. propose that their criteria should be applied only after any other disease has been ruled out.[4] In 2008 a consensus was developed for differential diagnosis.[9]

Another criticism of the McDonald criteria is that the definition of "lesions typical of MS" is unclear; a 2013 review identified the following characteristics: specific cell morphology shown by hematoxylin, demyelination shown by Luxol fast blue, macrophage appearance by KiM1P or CD68, damage to the axons shown by Bielschowsky stain, astrocytopathy shown by glial fibrillary acidic protein, and different lymphocyte subtypes, reacting to CD3, CD4, CD8, CD20 and CD138.[10]

The sensitivity of McDonald criteria is low with regard to pathologically defined MS because around 25% of MS cases are silent MS cases.[11]

McDonald criteria have been shown to have a low sensitivity and specificity (with respect to the pathological presence of lesions) in Asiatic populations.[12][13] They have good predictive quality (with respect to CIS [clinically isolated syndrome] to CDMS [Clinically Definite Multiple Sclerosis] conversion) when evaluated in non-selected populations.[14]

Comparison of McDonald versions

Currently there is not too much information comparing the sensibility and specificity of different McDonald versions against autopsy. Some reports have used Poser "CDMS" delayed diagnosis (during a two-year follow-up) as milestone to evaluate these parameters.

It seems that 2017 revision has higher sensitivity (85 vs. 30% and 85 vs. 41%) and lower specificity (33 vs. 63% and 63 vs. 85%) compared to the 2010 revisions and Poser CDMS,[15] at two years follow-up.

2010 Revisions

In 2010, the International Panel on Diagnosis of MS met in Dublin, Ireland for a third time to discuss and revise the McDonald diagnostic criteria.[2] Reasons for revisions to the criteria included the simplification of demonstration of CNS lesions in space and time via imaging, and to address criticisms that the previous criteria did not appropriately apply to Asian populations.[2]

One study has suggested that the new criteria allow a faster diagnosis, but with slight sacrifice in accuracy.[16]

Revised Diagnostic Criteria (2010)

Clinical Presentation Additional Data Needed
* 2 or more attacks (relapses)
* 2 or more objective clinical lesions 		None; clinical evidence will suffice (additional evidence desirable but must be consistent with MS)
* 2 or more attacks
* 1 objective clinical lesion 		Dissemination in space, demonstrated by:
* MRI
* or further clinical attack involving different site.
New criteria: Dissemination in Space (DIS) can be demonstrated by the presence of 1 or more T2 lesions in at least 2 of 4 of the following areas of the CNS: Periventricular, Juxtacortical, Infratentorial, or Spinal Cord.
* 1 attack
* 2 or more objective clinical lesions 		Dissemination in time (DIT), demonstrated by:
* MRI
* or second clinical attack
New criteria: No longer a need to have separate MRIs run; Dissemination in time, demonstrated by: Simultaneous presence of asymptomatic gadolinium-enhancing

and nonenhancing lesions at any time; or A new T2 and/or gadolinium-enhancing lesion(s) on follow-up MRI, irrespective of its timing with reference to a baseline scan; or Await a second clinical attack. [This allows for quicker diagnosis without sacrificing specificity, while improving sensitivity.]

* 1 attack
* 1 objective clinical lesion
(clinically isolated syndrome) 		New criteria: Dissemination in space and time, demonstrated by:

For DIS: 1 or more T2 lesion in at least 2 of 4 MS-typical regions of the CNS (periventricular, juxtacortical, infratentorial, or spinal cord); or Await a second clinical attack implicating a different CNS site; and For DIT: Simultaneous presence of asymptomatic gadolinium-enhancing and nonenhancing lesions at any time; or A new T2 and/or gadolinium-enhancing lesion(s) on follow-up MRI, irrespective of its timing with reference to a baseline scan; or Await a second clinical attack.

Insidious neurological progression
suggestive of MS
(primary progressive MS) 		New criteria: One year of disease progression (retrospectively or prospectively determined) and

two or three of the following:
1. Evidence for DIS in the brain based on 1 or more T2 lesions in the MS-characteristic (periventricular, juxtacortical, or infratentorial) regions
2. Evidence for DIS in the spinal cord based on 2 or more T2 lesions in the cord
3. Positive CSF (isoelectric focusing evidence of oligoclonal bands and/or elevated IgG index)

2017 revision

The last revision (as of 2018) is the 2017 revision.[6] It has been reported to improve sensibility up to an 82% (respect around 8 years CIS to MS conversion, retrospectively evaluated). The 2017 revision predicted 86.8% of positives in the follow-up using as reference the 2010 criteria after a follow-up of 3.8 ± 2.9 years.[17] No reduction in specificity was reported.

The 2017 revision tries to accelerate the diagnosis without risking specificity. The new recommendations include:[6]

  • First of all, probably the most polemical change, a patient with CIS (only one demyelinating lesion) can now be diagnosed as MS if an MRI shows dissemination in space (DIS). In these cases dissemination in time (DIT) can be substituted by a laboratory testing of oligoclonal bands.
  • Second, both symptomatic and asymptomatic lesions can be considered for showing DIS and DIT
  • Third, also cortical lesions can be used to show DIS.
  • Fourth, also for PPMS cortical and asymptomatic lesions can be used in diagnosis.

Future directions

Improvements in imaging technology

MRI results do not pick up all MS lesions.[18] The European group MAGNIMS periodically publishes guidelines for using MRI in the diagnosis of MS that are updated as MRI technology evolves.[19][third-party source needed] Moreover, new MRI techniques, such as double inversion recovery imaging or phase sensitive inversion recovery, can be used to identify more lesions in MS which, if further validated, could be included in future criteria. Another promising MRI technique is magnetic transfer imaging, which will allow the detection of damage in normal-appearing brain tissue away from focal lesions. Finally, high resolution spectral domain optical coherence tomography could prove to be a very promising and sensitive way of identifying optic neuritis in the future.[5]

Improvements in biomarkers

Four biomarkers were identified for further study by the 2010 revisions of McDonald Criteria: The CSF,[20] the serum anti-GAGA4[21] and protein signatures[22] and finally the circulating microRNA[23] Some blood tests have been proposed based in circulating neurofilament light chain (NFL), in RNA profiling[24] or in the MRZ reaction.

Addressing subclinical disease

Another issue of great clinical significance that is not addressed by 2010 McDonald criteria is subclinical disease. There are some patients who were incidentally found to have brain lesions with appearance and location consistent with MS who are now classified as having a radiologically isolated syndrome (RIS). Some of these people will develop MS even after several years. Because early initiation of MS disease-modifying therapy is associated with better clinical outcomes, it is important to identify individuals in the subclinical stage of disease and determine if initiation of treatment at this stage is beneficial. More research is currently being conducted to clarify this issue and address which RIS patients will progress to definite MS. Depending on the findings of this research, future criteria might address this controversial but highly important issue of MS care.[5]

References

  1. ↑ 1.0 1.1 Polman, Chris H; Reingold, Stephen C; Edan, Gilles; Filippi, Massimo; Hartung, Hans-Peter; Kappos, Ludwig; Lublin, Fred D; Metz, Luanne M et al. (2005). "Diagnostic criteria for multiple sclerosis: 2005 revisions to the 'McDonald Criteria'". Annals of Neurology 58 (6): 840–6. doi:10.1002/ana.20703. PMID 16283615. 
  2. ↑ 2.0 2.1 2.2 2.3 Polman, Chris H; Reingold, Stephen C; Banwell, Brenda; Clanet, Michel; Cohen, Jeffrey A; Filippi, Massimo; Fujihara, Kazuo; Havrdova, Eva et al. (2011). "Diagnostic criteria for multiple sclerosis: 2010 Revisions to the McDonald criteria". Annals of Neurology 69 (2): 292–302. doi:10.1002/ana.22366. PMID 21387374. 
  3. ↑ Thompson, Alan J; Banwell, Brenda L; Barkhof, Frederik; Carroll, William M; Coetzee, Timothy; Comi, Giancarlo; Correale, Jorge; Fazekas, Franz et al. (2018). "Diagnosis of multiple sclerosis: 2017 revisions of the Mc Donald criteria". The Lancet Neurology 17 (2): 162–173. doi:10.1016/S1474-4422(17)30470-2. PMID 29275977. http://discovery.ucl.ac.uk/10041020/1/Barkhof_Diagnostic%20criteria_revision%201_final_10OCT2017.pdf. 
  4. ↑ 4.0 4.1 4.2 McDonald, W. Ian; Compston, Alistair; Edan, Gilles; Goodkin, Donald; Hartung, Hans-Peter; Lublin, Fred D; McFarland, Henry F; Paty, Donald W et al. (2001). "Recommended diagnostic criteria for multiple sclerosis: Guidelines from the international panel on the diagnosis of multiple sclerosis". Annals of Neurology 50 (1): 121–7. doi:10.1002/ana.1032. PMID 11456302. 
  5. ↑ 5.0 5.1 5.2 5.3 Ntranos, Achilles; Lublin, Fred (2016). "Diagnostic Criteria, Classification and Treatment Goals in Multiple Sclerosis: The Chronicles of Time and Space". Current Neurology and Neuroscience Reports 16 (10): 90. doi:10.1007/s11910-016-0688-8. PMID 27549391. 
  6. ↑ 6.0 6.1 6.2 Thompson, Alan J; Banwell, Brenda L; Barkhof, Frederik; Carroll, William M; Coetzee, Timothy; Comi, Giancarlo; Correale, Jorge; Fazekas, Franz et al. (2018). "Diagnosis of multiple sclerosis: 2017 revisions of the Mc Donald criteria". The Lancet Neurology 17 (2): 162–173. doi:10.1016/S1474-4422(17)30470-2. PMID 29275977. http://discovery.ucl.ac.uk/10041020/1/Barkhof_Diagnostic%20criteria_revision%201_final_10OCT2017.pdf. 
  7. ↑ P. Brex, V. Williams, Updated criteria for diagnosing Multiple Sclerosis, ACNR, VOLUME 18 NUMBER 2, NOVEMBER-JANUARY 2019
  8. ↑ Lassmann Hans (2010). "Acute disseminated encephalomyelitis and multiple sclerosis". Brain 133 (Pt 2): 317–319. doi:10.1093/brain/awp342. PMID 20129937. 
  9. ↑ "Differential diagnosis of suspected multiple sclerosis: a consensus approach". Mult Scler 14 (9): 1157–1174. 2008. doi:10.1177/1352458508096878. PMID 18805839. 
  10. ↑ Popescu, Bogdan F. Gh; Pirko, Istvan; Lucchinetti, Claudia F (2013). "Pathology of Multiple Sclerosis". CONTINUUM: Lifelong Learning in Neurology 19 (4 Multiple Sclerosis): 901–21. doi:10.1212/01.CON.0000433291.23091.65. PMID 23917093. 
  11. ↑ Engell T (May 1989). "A clinical patho-anatomical study of clinically silent multiple sclerosis". Acta Neurol Scand 79 (5): 428–30. doi:10.1111/j.1600-0404.1989.tb03811.x. PMID 2741673. 
  12. ↑ HT Chong et al (2006) Proposed modifications to McDonald diagnostic criteria for Asians with multiple sclerosis, Neurology Asia 11:87–90
  13. ↑ Chong, H; Kira, J; Tsai, C; Ong, B; Li, P; Kermode, A; Tan, C (19 June 2009). "Proposed modifications to the McDonald criteria for use in Asia". Multiple Sclerosis 15 (7): 887–888. doi:10.1177/1352458509104587. PMID 19542266. 
  14. ↑ Fortini, Alexandre S.; Sanders, Elizabeth L.; Weinshenker, Brian G.; Katzmann, Jerry A. (1 November 2003). "Cerebrospinal Fluid Oligoclonal Bands in the Diagnosis of Multiple Sclerosis Isoelectric Focusing With IgG Immunoblotting Compared With High-Resolution Agarose Gel Electrophoresis and Cerebrospinal Fluid IgG Index". American Journal of Clinical Pathology 120 (5): 672–675. doi:10.1309/Y5VFF2UAW0RK5W63. PMID 14608891. 
  15. ↑ Habek M, Establishing (Jul 2018). "2010 versus 2017 McDonald criteria". Mult Scler Relat Disord 25: 99–103. doi:10.1016/j.msard.2018.07.035. PMID 30059896. http://medlib.mef.hr/3506/1/habek_m_et_al_rep_3506.pdf. 
  16. ↑ Runia, TF; Jafari, N; Hintzen, RQ (December 2013). "Application of the 2010 revised criteria for the diagnosis of multiple sclerosis to patients with clinically isolated syndromes.". European Journal of Neurology 20 (12): 1510–6. doi:10.1111/ene.12243. PMID 23906114. 
  17. ↑ Gaetani L, Prosperini L, Mancini A, Eusebi P, Cerri MC, Pozzilli C, Calabresi P, Sarchielli P, Di Filippo M (2017). "revisions of McDonald criteria shorten the time to diagnosis of multiple sclerosis in clinically isolated syndromes". J Neurol 265 (11): 2684–2687. doi:10.1007/s00415-018-9048-8. PMID 30196327. 
  18. ↑ McDonald criteria
  19. ↑ Filippi, Massimo; Rocca, Maria A; Ciccarelli, Olga; De Stefano, Nicola; Evangelou, Nikos; Kappos, Ludwig; Rovira, Alex; Sastre-Garriga, Jaume et al. (2016). "MRI criteria for the diagnosis of multiple sclerosis: MAGNIMS consensus guidelines". The Lancet Neurology 15 (3): 292–303. doi:10.1016/S1474-4422(15)00393-2. PMID 26822746. 
  20. ↑ Awad, Amer; Hemmer, Bernhard; Hartung, Hans-Peter; Kieseier, Bernd; Bennett, Jeffrey L; Stuve, Olaf (2010). "Analyses of cerebrospinal fluid in the diagnosis and monitoring of multiple sclerosis". Journal of Neuroimmunology 219 (1–2): 1–7. doi:10.1016/j.jneuroim.2009.09.002. PMID 19782408. 
  21. ↑ Brettschneider, Johannes; Jaskowski, Troy D; Tumani, Hayrettin; Abdul, Sana; Husebye, Dee; Seraj, Haniah; Hill, Harry R; Fire, Ella et al. (2009). "Serum anti-GAGA4 IgM antibodies differentiate relapsing remitting and secondary progressive multiple sclerosis from primary progressive multiple sclerosis and other neurological diseases". Journal of Neuroimmunology 217 (1–2): 95–101. doi:10.1016/j.jneuroim.2009.07.017. PMID 19879655. 
  22. ↑ "Antigen microarrays identify unique serum autoantibody signatures in clinical and pathologic subtypes of multiple sclerosis". Proc Natl Acad Sci U S A 105 (48): 18889–18894. 2008. doi:10.1073/pnas.0806310105. PMID 19028871. Bibcode: 2008PNAS..10518889Q. 
  23. ↑ "Multiple sclerosis: microRNA expression profiles accurately differentiate patients with relapsing-remitting disease from healthy controls". PLOS ONE 4 (10): e7440. 2009. doi:10.1371/journal.pone.0007440. PMID 19823682. Bibcode: 2009PLoSO...4.7440K. 
  24. ↑ Nickles D et al., Blood RNA profiling in a large cohort of multiple sclerosis patients and healthy controls, Hum Mol Genet. 2013 Oct 15;22(20):4194-205. doi: 10.1093/hmg/ddt267. Epub 2013 Jun 6.



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