Coronary anomalies of the left anterior descending artery (LAD) are very rare, with a frequency of less than 1% in the general population.[1] Most patients with LAD anomalies are asymptomatic, and therefore most are discovered incidentally. However, some anomalies of the LAD put patients at risk for myocardial dysfunction, myocardial infarction, ventricular arrhythmias, and even sometimes produce a steal phenomenon. These potentially life-threatening coronary artery anomalies need to be identified and treated promptly to lower the risk of morbidity and mortality. Traditionally, the percutaneous transcatheter arteriography (PCA) was the recommended diagnostic test of choice. However, now with advancement in technology, the electrocardiographically (ECG)–gated multi-detector row computed tomography (CT) is the preferred method of diagnosis an anomalous LAD.[2] The CT scan allows for the accurate and noninvasive depiction of coronary artery anomalies of origin, course, and termination. Treatment modalities vary by the type of LAD anomaly present. Some require surgical intervention or transcatheter intervention, while others require only medical therapy or observation. This article will describe in detail the normal structure and function of the LAD, embryologic anomalies of the LAD, surgical considerations, and clinical significance of anomalous LAD.

Normal Anatomy of the LAD

The normal origin of the LAD is at the bifurcation of the distal left main coronary artery (LMCA). From there, it travels around the left side of the pulmonary artery (PA) and passes into the epicardial fat obliquely in the direction of the apex of the heart in the anterior interventricular sulcus. The LAD is made up of a proximal segment, middle segment, and distal segment. The proximal segment contains the first branch of the septal perforator. The middle segment is bordered by the first septal branch and represents the halfway point between the septal branch and the ventricular apex. The distal segment is from the halfway point to the apex. The length of the LAD usually measures approximately 10 cm to 13 cm long. Branches of the LAD are called diagonal branches and septal perforator branches. There are usually one or two large diagonal branches that may arise and descend diagonally across the anterior surface of the LV. The septal perforator branches supply the anterior two-thirds of the basal interventricular septum and the entire septum at the mid and apical levels.[2]

Anomalies of Origin

The most common coronary artery anomalies of the LAD are congenital abnormalities of the origin. One of the most dangerous anomalies of origin of the LAD is when the LAD originates off the pulmonary artery, which is a very rare anomaly that can lead to myocardial injury and potential death.[3] Patients tend to experience symptoms early in life. Approximately 90% of untreated infants die in the 1st year of life, and only a few patients survive to adulthood.[4] Another potentially fatal LAD anomaly is when the LAD is the only coronary artery to arise with a single ostium from the aortic trunk, called a single coronary artery.[5] Population studies reveal a frequency of single LAD to be less than 0.0024 to 0.044%. [6] These patients are at increased risk of sudden cardiac death (SCD), especially if the vessel takes an inter-atrial path, or passes between the aorta and pulmonary artery. Another anomaly of origin of the LAD is when the LAD originates from the RCA; this correlates with the tetralogy of Fallot. The LAD can also originate from the right sinus of Valsalva and has been known to correlate with double outlet right ventricle, tetralogy of Fallot, and transposition complexes. Sometimes these occur in the congenital absence of the LMCA. The absence of the LMCA is associated with aortic valve disease and left dominance. When the LMCA is atretic, a fibrous connection may be seen between the LAD, left circumflex (LCx) arterial junction, and the left sinus of Valsalva. The LAD and the LCx are found on rare occasions to branch from the same origin and bifurcate at the same time; this is called multiple Ostia. Patients with multiple Ostia coronary anomalies are a high risk of coronary artery disease in the affected vessels.[7] While there can be multiple Ostia in some patients, rarely there can also be congenital ostial stenosis or atresia.[8] This condition can be a life-threatening congenital anomaly when it involves the LAD unless there is sufficient collateral supply to the LAD cardiac muscle domain.

Anomalies of Course

There are five different possible paths by which the coronary arteries can connect with the opposite coronary cusps. These paths are called pre-pulmonic, petro-aortic, inter-atrial, trans-septal, and retro-cardiac. The LAD is more commonly associated with the transeptal path; however, it can also be involved with all the other paths. The trans-septal path is when the coronary artery has a subpulmonic course as the artery travels anteriorly and inferiorly through the interventricular septum and takes an intramyocardial course, giving off septal branches and finally emerging at its normal epicardial position.[9]

Sometimes arteries are duplicated. The LAD has been noted in the literature to be a duplicate in 0.13% to 1% of the general population. It is noteworthy that sometimes one of the duplicated LAD arteries may arise from the RCA and take a pre-pulmonic, septal or inter-arterial course. Dual LAD is associated with congenital heart disease, most commonly Tetralogy of Fallot and transposition of the great vessels. One case report by Belostotsky et al. depicts a dual LAD from the LMCA and the other from the right aortic sinus of Valsalva.[10] This anomaly is not intrinsically hemodynamically significant, but its presence may complicate surgical intervention when aortocoronary bypass or other coronary artery surgery is performed.

Angiographic classification of dual LADs was a proposal by Spinaldo-Franco et al. According to Spinaldo-Franco et al. there are four types of dual LADs. Type I dual LAD has a short and long arm, both of which travels in the anterior interventricular sulcus (AIVS). The shorter LAD usually branches into all the major proximal septal perforators. The longer LAD travels on the left-ventricular side of the AIVS and then reenters the distal AIVS to reach the apex. Type II dual LAD has a similar short LAD as seen in Type I. The long arm, however, travels on the right ventricular side before reentering the AIVS to supply the apex. Type III also has a short arm similar to Type I, but the long arm descends intramyocardially into the septum. Type IV the long arm arises from the RCA.[11]  Manchanda et al. described another variant termed a type V dual LAD where the shorter LAD originates independently, starting from the left coronary sinus, and the longer LAD originates from the right sinus separate from the right coronary artery and undergoes an intramyocardial course before reaching the distal interventricular groove.[12]

Anomalies Termination

Coronary fistulas occur about 0.3% to 0.87% in patients who undergo cardiac catheterization. In 60% of cases, these fistulae drain into the right heart chambers.[13] Coronary fistulas are communications between a coronary artery and either the cardiac chamber, coronary sinus, pulmonary artery, or superior vena cava (SVC). Fistulas that connect to the cardiac chamber are called coronary cameral fistulas. The LAD has been noted to form all of these fistula types.[14][15][16] Coronary fistulas correlate with an increased risk of bacterial endocarditis. There have also been rare cases of communication between the LAD and the systemic circulation through an anomalous coronary artery formation. Systemic communications also correlate with the presence of congenital heart disease.