Peripartum cardiomyopathy

disease
On this page

Also known as Meadows' syndromepostpartum cardiomyopathy

Summary

Peripartum cardiomyopathy (MONDO:0018920) is a disease and 12 clinical trials. Top therapeutic interventions include bromocriptine, sodium chloride, and sodium selenate. A subtype of non-familial dilated cardiomyopathy — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Prevalence: 6-9 / 10 000 (Singapore) [Orphanet-validated]
  • Phenotypes (HPO): 45
  • Clinical trials: 12

Clinical features

Epidemiology

Prevalence records

6 prevalence record(s), Orphanet:

TypeClassValueGeographyValidation
Prevalence at birth6-9 / 10 00089SingaporeValidated
Prevalence at birth1-9 / 100 0005JapanValidated
Prevalence at birth>1 / 1000334HaitiValidated
Prevalence at birth>1 / 1000100South AfricaValidated
Prevalence at birth1-5 / 10 00030WorldwideNot yet validated
Prevalence at birth1-5 / 10 00036United StatesNot yet validated

Signs & symptoms

Clinical features (HPO)

45 HPO clinical features (Orphanet curated; top 45 by frequency):

HPO IDTermFrequency
HP:0000822HypertensionFrequent (30-79%)
HP:0001635Congestive heart failureFrequent (30-79%)
HP:0001644Dilated cardiomyopathyFrequent (30-79%)
HP:0001649TachycardiaFrequent (30-79%)
HP:0001712Left ventricular hypertrophyFrequent (30-79%)
HP:0001962PalpitationsFrequent (30-79%)
HP:0002094DyspneaFrequent (30-79%)
HP:0002875Exertional dyspneaFrequent (30-79%)
HP:0005135Abnormal T-waveFrequent (30-79%)
HP:0010741Pedal edemaFrequent (30-79%)
HP:0011703Sinus tachycardiaFrequent (30-79%)
HP:0012378FatigueFrequent (30-79%)
HP:0012664Reduced left ventricular ejection fractionFrequent (30-79%)
HP:0012764OrthopneaFrequent (30-79%)
HP:0025169Left ventricular systolic dysfunctionFrequent (30-79%)
HP:0030848Elevated jugular venous pressureFrequent (30-79%)
HP:0001653Mitral regurgitationOccasional (5-29%)
HP:0001708Right ventricular failureOccasional (5-29%)
HP:0001907ThromboembolismOccasional (5-29%)
HP:0002092Pulmonary arterial hypertensionOccasional (5-29%)
HP:0004756Ventricular tachycardiaOccasional (5-29%)
HP:0005120Abnormal cardiac atrium morphologyOccasional (5-29%)
HP:0005133Right ventricular dilatationOccasional (5-29%)
HP:0006705Abnormal atrioventricular valve morphologyOccasional (5-29%)
HP:0012398Peripheral edemaOccasional (5-29%)
HP:0012763Paroxysmal dyspneaOccasional (5-29%)
HP:0012819MyocarditisOccasional (5-29%)
HP:0030148Heart murmurOccasional (5-29%)
HP:0030356Increased serum interferon-gamma levelOccasional (5-29%)
HP:0030830CracklesOccasional (5-29%)
HP:0031295Left atrial enlargementOccasional (5-29%)
HP:0100602PreeclampsiaOccasional (5-29%)
HP:0100603Toxemia of pregnancyOccasional (5-29%)
HP:0100749Chest painOccasional (5-29%)
HP:0000819Diabetes mellitusVery rare (<1-4%)
HP:0001513ObesityVery rare (<1-4%)
HP:0001903AnemiaVery rare (<1-4%)
HP:0002027Abdominal painVery rare (<1-4%)
HP:0002099AsthmaVery rare (<1-4%)
HP:0002401Stroke-like episodeVery rare (<1-4%)
HP:0002878Respiratory failureVery rare (<1-4%)
HP:0002926Abnormality of thyroid physiologyVery rare (<1-4%)
HP:0002960AutoimmunityVery rare (<1-4%)
HP:0011713Left bundle branch blockVery rare (<1-4%)
HP:0030149Cardiogenic shockVery rare (<1-4%)

Identifiers

Disease identifiers

FieldValue
Canonical nameperipartum cardiomyopathy
Mondo IDMONDO:0018920
EFOEFO:0002628
Orphanet563
DOIDDOID:9997
ICD-10-CMO90.3
ICD-111218807936
NCITC171602
SNOMED CT62377009
UMLSC0877208
MedGen163756
GARD0000220
MedDRA10049430
Is cancer (heuristic)no

Also known as: Meadows’ syndrome · peripartum cardiomyopathy · postpartum cardiomyopathy

Data availability: 4 cell lines.

Disease family

Classification path: disease › human disease › disease by body system or component › musculoskeletal system disordermuscle tissue disordercardiomyopathyintrinsic cardiomyopathydilated cardiomyopathy › non-familial dilated cardiomyopathy › peripartum cardiomyopathy

Related subtypes (1): cirrhotic cardiomyopathy

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

Drugs indicated for this disease

0 approved, 1 in late-stage (phase 3) trials. Disease-direct ChEMBL indications, not inferred from the associated-gene cohort below.

DrugDevelopment status
BromocriptinePhase 3 (in late-stage trials)

Earlier-phase candidates (phase 2, investigational — efficacy not yet established): Sodium Chloride.

Clinical trials & evidence

Clinical trials

Clinical trials: 12.

Phase distribution (across all retrieved trials)

PhaseTrials
Not specified8
PHASE41
PHASE31
PHASE2/PHASE31
PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT03081949PHASE4COMPLETEDPeripartum Cardiomyopathy in Nigeria Registry
NCT02590601PHASE3WITHDRAWNBromocriptine in the Treatment of Peripartum Cardiomyopathy
NCT03907267PHASE2/PHASE3COMPLETEDTaurine in Peripartum Cardiomyopathy
NCT00998556PHASE2COMPLETEDEffect of Bromocriptine on Left Ventricular Function in Women With Peripartum Cardiomyopathy
NCT06607471Not specifiedRECRUITINGMultimodal and Multidisciplinary Approach to Optimize Diagnostic, Prognostic, and Therapeutic Management of Patients with Non-ischemic Cardiomyopathies and Arrhythmogenic-inflammatory Phenotypes: a Multicenter, Observational, Retrospective and Prospective Registry Study.
NCT03364140Not specifiedUNKNOWNA Registry of Peripartum Cardiomyopathy in Turkey
NCT04049136Not specifiedCOMPLETEDNT-proBNP Levels and Obesity in Pregnancy
NCT04143997Not specifiedWITHDRAWNDiastolic Dysfunction PPCM in Patients With Documented Left Ventricular Systolic Function Recovery
NCT04144660Not specifiedCOMPLETEDTreatment Use of ECMO In Pregnancy or Peripartum Patient.
NCT04234659Not specifiedCOMPLETEDPPCM Observational Study (Peripartum Cardiomyopathy)
NCT04927715Not specifiedUNKNOWNIrisin Expression and Gene Polymorphism With Peripartum Cardiomyopathy.
NCT05878041Not specifiedUNKNOWNCreation of a Multicenter National Registry for Peripartum Cardiomyopathy.

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
BROMOCRIPTINE46
SODIUM CHLORIDE41
SODIUM SELENATE31
SODIUM SELENITE31
TAURINE31
CHEMBL162514102
CHEMBL420647602
CHEMBL420692502